The Gut-Immune-Brain Axis in Autism Spectrum Disorders; A Focus on Amino Acids
- 1Division of Pharmacology, Utrecht Institute for Pharmaceutical Sciences, Faculty of Science, Utrecht University, Utrecht, Netherlands
- 2Danone Nutricia Research, Utrecht, Netherlands
- 3Laboratory of Neuroimmunology, Department of Symptom Research, The University of Texas MD Anderson Cancer Center, Houston, TX, United States
- 4Veterinary Pharmacology, Institute for Risk Assessment Studies, Faculty of Veterinary Sciences, Utrecht University, Utrecht, Netherlands
Autism spectrum disorder (ASD) is a range of neurodevelopmental conditions that affect communication and social behavior. Besides social deficits, systemic inflammation, gastrointestinal immune-related problems, and changes in the gut microbiota composition are characteristic for people with ASD. Animal models showed that these characteristics can induce ASD-associated behavior, suggesting an intimate relationship between the microbiota, gut, immune system and the brain in ASD. Multiple factors can contribute to the development of ASD, but mutations leading to enhanced activation of the mammalian target of rapamycin (mTOR) are reported frequently. Hyperactivation of mTOR leads to deficits in the communication between neurons in the brain and to immune impairments. Hence, mTOR might be a critical factor linking the gut-brain-immune axis in ASD. Pharmacological inhibition of mTOR is shown to improve ASD-associated behavior and immune functions, however, the clinical use is limited due to severe side reactions. Interestingly, studies have shown that mTOR activation can also be modified by nutritional stimuli, in particular by amino acids. Moreover, specific amino acids are demonstrated to inhibit inflammation, improve gut barrier function and to modify the microbiota composition. In this review we will discuss the gut-brain-immune axis in ASD and explore the potential of amino acids as a treatment option for ASD, either via modification of mTOR activity, the immune system or the gut microbiota composition.
The Gut-Brain Axis in Autism Spectrum Disorder
Autism spectrum disorder (ASD) is a spectrum of neurological disorders that become apparent in early childhood and last throughout a person's life. This spectrum of disorders is characterized by varying levels of deficits in social behavior and communication, as well as stereotypical behaviors (1). Estimates of the prevalence of ASD vary widely among different studies, largely attributable to differences in diagnostic criteria, the ages and gender of the children screened, as well as the geographical location (2). Meta-analyses comprising studies in different geographical locations indicate a global incidence of ASD between 0.6 and 0.7% (3, 4). Over the past decades, the reported global prevalence has increased markedly (4, 5). Studies suggest that part of this increase is attributable to changes in diagnostic criteria, an increased awareness and the ability to diagnose at a younger age (3, 6). However, these changes alone are not sufficient to explain the rise in ASD prevalence. Other factors, including prenatal, natal and postnatal environmental factors like diet, intestinal microbiota, and immunological triggers are likely to also contribute to this increase (7–9).
In addition to behavioral deficits, autistic individuals often present with mild systemic inflammation and gastrointestinal disorders (10, 11). Although current epidemiological data is limited, a recent meta-analysis confirms that children with ASD experience four times more gastrointestinal symptoms than control groups and that gastrointestinal symptoms may identify a unique subgroup of children with ASD (12). Moreover, numerous studies showed a link between immune disturbances and ASD (11, 13, 14). Although research into the relation between immune disturbances and ASD is still in its early phases, studies suggest that many different aspects of the immune system are involved (15–17). For instance, ASD has been associated with a deregulated activation of microglia and astroglia (the “immune-like” cells in the brain) (18, 19), autoimmunity (20), increased T cell activation (21), deregulated innate immune functioning (11) and mutations in genes controlling the functioning of immune cells (11, 22, 23). The deregulated immune functions in people with ASD are reflected by abnormal cytokine levels in their body fluids. More specifically, levels of pro-inflammatory and allergy-associated type 2 helper T (Th2) cell-derived cytokines (e.g., TNFα, IL-4, IL-5, IL-6, IL-8) are shown to be upregulated in either cerebrospinal fluid, plasma or serum of people with ASD (21), whereas levels of regulatory cytokines IL-10 and TGF-β are downregulated (24–26). Multiple studies investigated the relation between the aberrant cytokine levels and autism. One example is a study performed by Hashim et al. (27). Here, it was shown that serum levels of TGF-β negatively correlated with the severity of autistic symptoms. A similar negative correlation was found between the severity of autism and the frequency of regulatory T (Treg) cells in blood, which appears to be lower in autistic individuals (28). As TGF-β plays a critical role in Treg cell development (29), there might be a causal relation between lower TGF-β levels, lower Treg levels and autism severity. Besides its role in the development of Treg cells, TGF-β is also indicated to play an important role in brain development (30, 31). More specifically, TGF-β regulates survival and differentiation of neurons and directs the growth of synapses, as observed in various invertebrate models (30, 31). Hence, a lack of TGF-β could contribute to dysregulated brain functioning, representing another mechanism by which aberrant TGF-β levels could be involved in the development of autistic phenotypes observed in autistic patients. The presence of a relation between abnormal cytokine levels in autistic individuals and autism severity is further corroborated by two large studies in children with ASD (32, 33). In these studies it was demonstrated that the increase of a broad range of cytokines including pro-inflammatory, Th2 as well as type 1 helper T (Th1) cell-derived cytokines and chemokines correlates with aberrant (autistic) behavior and impaired development (32, 33).
The exact mechanisms underlying the increased production of pro-inflammatory cytokines and allergy-associated Th2 cytokines in autistic individuals are yet to be elucidated. However, a potential explanation of these findings might be sought in the observation that allergy, especially food allergy, and eosinophilic esophagitis are often reported in ASD patients (34, 35). A food-induced allergic disease is an unfavorable immune reaction that can occur on exposure to specific food components, particularly proteins (36). Classically, food allergy is regarded as a type 1 hypersensitivity, i.e., an IgE-mediated immune response to harmless food proteins (Figure 1).
Figure 1. In the first phase of allergy or type 1 hypersensitivity reactions sensitization to the food allergen takes place (sensitization phase). During this phase, allergens cross the intestinal mucosal barrier and are presented via MHC-II to naïve T cells that develop into type 2 helper T (Th2) cells. Th2 cells induce the plasma cells to produce IgE antibodies (37), after which IgE binds to the FcεRI receptor on mast cells. In the challenge phase, upon a second exposure to the same allergen, cross-linking of mast cell-bound IgE occurs. In turn, this leads to mast cell degranulation, a process resulting in the release of several mediators including histamine, cytokines and tryptases. The release of these mediators is the direct cause of most of the allergic intestinal symptoms, including nausea, vomiting, cramps, and diarrhea (38). With permission of Dr J. Wu.
The Immune-Brain Axis in ASD With a Focus on Food Allergy
It has been shown from parental reports that food allergies are observed more often in autistic individuals than in the general population (39–41). This differential occurrence of food allergies might be even more evident than reported, since impaired communication by autistic individuals could lead to underdiagnoses (39). Multiple studies investigated the relation of food allergies with ASD. For instance, it has been reported that autistic children have higher serum levels of IgA, IgG, and IgM specific for cow's milk proteins compared to healthy controls (42, 43). Interestingly, Lucarelli et al. showed that autistic children on a cow's milk free diet showed improved behavioral symptoms (43). Vice versa, challenging autistic individuals with cow's milk led to an increase in hallmark behaviors associated with ASD, providing evidence for a relation between food allergic reactions and behavior (43). Preclinical studies provide further evidence for a relation between food allergies and ASD, as cow's milk allergic (CMA) mice show autistic-like behavior such as reduced social interaction, increased repetitive behavior, disturbed spatial memory and reduced exploration behavior (44). The changes in behavior of CMA mice were associated with increased neuronal activation in the prefrontal cortex (PFC). Similarly, patients with ASD show enhanced neuronal activation in the PFC in response to tasks involving facial recognition (45) and attention (46). Furthermore, the activation of the dopaminergic system in the PFC of CMA mice was reduced as compared to non-allergic mice (44). Interestingly, in mouse models for ASD as well as in patients with ASD, dampening of the dopaminergic system in the PFC is observed as well (47–49). Taken together, it can be hypothesized that intestinal allergic responses may affect brain circuits involved in social behavior in ASD patients with food allergies.
A variety of studies examined the underlying mechanism of the apparent relation between the induction of food allergy and autistic behavior. As described earlier, individuals with ASD are associated with a pro-inflammatory cytokine profile in various body fluids and a disbalance in Th2 and Treg cells, which are common features for allergic individuals as well (21, 27, 32). Besides differences involving T cells, ASD is also associated with deviations involving the activation of mast cells, which are cells that, upon activation, play a central role in driving allergic reactions. For instance, mast cell activation is shown to be increased in ASD patients, resulting in elevated release of inflammatory and neurotoxic mediators, which in turn could contribute to the development of autistic phenotypes (14, 50, 51). The influence of mast cells on behavior is not limited to the effects of mediator-release, as mast cells can also influence behavior via direct mast cell-neuron interactions, which take place in the brain (52) and the gut (53, 54). The potential of mast cell abnormalities to drive ASD-associated behavior in human is supported by a study performed by Theoharides et al. (55). In this study, the occurrence of mastocytosis, as characterized by the presence of proliferating and hyperactivated mast cells in several organs, is investigated in children with ASD (55). This study indicated that the incidence of mastocytosis is ten times higher in ASD patients than in the general population (55). In addition, 15% of the people who suffered from mastocytosis showed aberrant behaviors, such as concentration problems, decreased attention span, memory impairment, irritation, and distraction (55). These abnormal behaviors are similar to those encountered in ASD, suggesting that hyperactivation of mast cells, as occurs during allergic reactions, might be one of the mechanisms underlying the relation between food allergies and ASD-associated behavior. The potential involvement of mast cell hyperactivation in inducing ASD-associated behavior is further supported by studies showing that mast cell hyperactivation is associated with increased intestinal permeability (55). Accordingly, it is frequently reported that people with ASD have an increased intestinal permeability (56, 57). This disruption of the intestinal barrier might be involved in inducing ASD-like behavior, as preclinical research demonstrated that animals with ASD who suffer from defects in the intestinal barrier show increased levels of bacterial toxins in the bloodstream, which in turn could influence brain function (58).
The Mammalian Target of Rapamycin in ASD and its Connection With the Immune System
ASD is thought to be a neurodevelopmental disorder caused by multiple genetic and environmental factors. The genes involved in ASD are variable and diverse, but mutations in genes related to the mammalian target of rapamycin (mTOR) pathway, including NF1 (59), PTEN (60), TSC1 (61), TSC2 (62), eIF4E (63), FMRP (64), are among those most widely associated with ASD (Figure 2).
Figure 2. Schematic representation of the mTOR-signaling pathway in ASD. Mutations in various components involved in the mTOR signaling pathway such as PTEN, Nf1, TSC, eIF4E, FMRP (indicated by red circles) affect the protein synthesis machinery, leading to the development of ASD. Adapted from Ehninger et al. (62, 65). With permission of Dr. J. Wu.
NF1, PTEN, and TSC1/TSC2 act as negative regulators of mTOR complex 1 (mTORC1), of which single gene mutations lead to enhanced mTOR activity in the brain in various mouse models (60, 62, 65). Enhanced activation of mTOR leads to an increase in the phosphorylation of proteins downstream of mTORC1, such as S6 kinase (S6K) and eIF4E-binding proteins (4E-BPs), thereby promoting cap-dependent protein translation (66, 67). In this way, enhanced mTOR activation leads to an increase in the translation of neuroligins (67), which are proteins that are involved in the formation and maintenance of synapses between neurons. In turn, this results in an increased synaptic excitation/inhibition ratio, which may contribute to the development of ASD phenotypes (67). Interestingly, apart from its important role in neurological disorders, the mTOR-signaling pathway is also involved in directing immune responses (Figure 3).
Figure 3. Schematic representation regarding the possible role of mTOR activity in the balance of T cell profiling in food allergy. Enhanced mTOR activity is required for Th1, Th2, and Th17 cell differentiation. Suppression of the mTOR activity induces the differentiation into Treg cells. Adapted from Delgoffe et al. (68) and Kim et al. (69). With permission of Dr J. Wu.
Several studies suggest that Th1 and T helper 17 (Th17) cell differentiation are specifically regulated by mTORC1 signaling, whereas Th2 cell differentiation depends on mTOR complex 2 (mTORC2) signaling (68, 70, 71). This is supported by studies that show that T cells in which mTORC2 activity is eliminated fail to differentiate into Th2 cells in vitro and in vivo, but are able to differentiate into Th1 and Th17 cells (72). When mTORC1 and mTORC2 are both inhibited using rapamycin, T cells differentiate into Treg cells (72). Indeed, rapamycin-induced mTOR inhibition resulted in elevated numbers of Treg cells in tissue culture of nasal polyps obtained from patients suffering from chronic allergic rhinitis (73). Further evidence of the ability of mTOR to direct immune responses is provided by a study by Kim et al. showing that mTORC1 activation in mast cells is associated with survival, differentiation, migration, and cytokine production (69). Finally, increased mTOR activity is shown to attenuate autophagy (74) which, in the intestine, is an important process to limit chronic intestinal inflammation (75). Thus, hyperactivity of mTOR in the intestinal tract might lead to a loss of immune regulation and barrier integrity, leading to an inflammatory profile possibly associated with allergy. Taken together, these findings reveal that in ASD the mTOR signaling pathways could be disturbed at the level of the immune system, the gastro-intestinal tract as well as the brain. As such, the mTOR signaling pathways could be considered as a central point in the gut-immune-brain axis. Manipulation of the mTOR signaling pathway may therefore serve as a therapeutic strategy for inflammation-associated neurodevelopmental disorders including ASD.
In order to more specifically investigate the role of mTOR in ASD, a variety of mTOR-inhibitors have been used. The mTOR inhibitor that is most commonly used for this purpose is rapamycin. Rapamycin interacts with the intracellular receptor FK506 binding protein (FKBP12). The formed FKBP12-rapapmycin complex binds to mTOR and directly inhibits mTORC1, while mTORC2 is inhibited indirectly in a manner not fully understood (76, 77). As described earlier, mTORC1 drives translation of proteins, like neuroligins, that increase autistic-like phenotypes (77). Therefore, inhibition of mTORC1 by rapamycin might represent a therapeutic strategy for ASD patients. Indeed, rapamycin treatment improved ASD-associated behavior in various animal models for ASD, including the widely used BTBRT(+)ltpr3(tf)/J mouse model (78–81). Moreover, rapamycin treatment was shown to inhibit the social behavioral deficits and normalize the repetitive self-grooming behavior of CMA mice (82). In these mice, the humoral immune responses and mucosal mast cell activation in the intestines were also inhibited (82). At the molecular level, several changes were observed in the intestines of rapamycin-treated CMA mice that might underlie the observed improvement in behavioral outcomes. For instance, it has been shown that rapamycin treatment inhibited the enhanced phosphorylation and activation of the downstream target of mTOR p70 ribosomal protein S6 kinase (p70S6K) in the small intestines (82). Moreover, rapamycin significantly increased the mRNA expression of forkhead box P3 (Foxp3) both in the ileum and the Peyer's Patches of CMA mice, indicating an increase in Treg cell development (82). Finally, rapamycin treatment increased the expression of Treg cell-associated cytokines, including IL-10 and TGF-β in the small intestine of CMA mice (82). Till this day, however, the effects of targeting mTOR on possible immune dysregulations found in the rodent ASD models mentioned above remain understudied.
Collectively, these data support the relevance to further investigate the therapeutic potential of mTOR inhibiting strategies in both genetic and idiopathic forms of ASD. However, the occurrence of serious side effects of chronic administration of pharmacological mTOR inhibitors like rapamycin, such as severe immunosuppression, is reason for concern and limits their potential as a viable treatment option for ASD (83, 84). Hence, safer alternative strategies to normalize mTOR activity are required.
Targeting ASD-Associated Abnormal mTOR Activity With Amino Acids
Besides pharmacological compounds, nutritional components are also able to modulate mTOR activity. Often described as being the most potent nutrition-derived modulators of mTOR are amino acids (AAs) (85, 86). Although it is not yet fully understood how AAs regulate mTOR activity, AA transporters seem to play a crucial role. A variety of mechanisms involving AA transporters are proposed by which AAs can regulate mTOR activity. First, AA transporters can form a passageway for AAs through the plasma membrane. Once inside the cell, the AAs activate cytoplasmic AA sensors by interacting with a multi-protein complex involving RAG GTPases, Ragulator, and the v-ATPase on the lysosomal surface (87–89). This interaction recruits mTORC1 to lysosomes, where it can be activated. One example of a cell-surface AA transporter is the well-studied heterodimeric CD98, which transports preferably branched chain AAs (BCAAs). In combination with a glutamine transporter (SLC1A5), CD98 exchanges leucine for glutamine to increase the intracellular leucine concentration which, in turn, activates mTORC1 through different signaling molecules (90). Another mechanism by which AAs can modulate mTORC1 activation involves a specific subset of AA transporters, known as AA transceptors, which have a dual transporter-receptor function. The binding or translocation of AAs by transceptors initiates an intracellular signaling cascade, ultimately leading to the modulation of mTORC1 activation (89, 91). Thus, AA transceptors can modulate mTORC1 activation by sensing the extracellular AA concentration. Finally, AAs can also modulate mTORC1 activity by mechanisms that do not involve the translocation of AAs across the plasma membrane (89, 91). Studies have demonstrated that specific AAs can bind and activate G-protein-coupled receptors, which in turn induce lysosomal localization and activation of mTORC1 (89). One example is the G protein-coupled receptor family C group 6 member A (GPRC6A), which is activated by basic, aliphatic and polar AAs such as serine, arginine and lysine.
As AAs can modulate mTORC1 activity via multiple mechanisms, which involve receptors and transceptors that specifically recognize different types of AAs, it is likely that the modulation of mTORC1 activity is different for each type of AA. Consistently, a previous study using mammary epithelial cells demonstrated that the BCAAs leucine (Leu), isoleucine (Ile), and valine (Val) enhanced mTORC1 activity, whereas histidine (His), lysine (Lys), and threonine (Thr) suppressed mTORC1 activity (92). Similar results were found in an in vitro allergic mast cell model (93). Inhibition of mTOR signaling by a combination of the AAs His, Lys and Thr in this mast cell model was accompanied by an inhibition of acute mast cell degranulation and an attenuated allergy-associated cytokine production following antigen-IgE mediated activation (93). Based on the outcomes of these in vitro studies, a diet containing relatively higher amounts of His, Lys and Thr and relatively lower amounts of Leu, Ile, and Val was developed for preclinical ASD studies (93). It was hypothesized that mTOR signaling could either be normalized or reduced in ASD animals using this AA diet. Consistent with this hypothesis, the AA diet restored the social interaction and normalized the repetitive behavior of CMA mice (93). In addition, dietary intervention with the AAs inhibited the enhanced mTOR signaling pathway in the PFC and amygdala of CMA mice. Since the mTOR signaling pathway is centrally involved in directing immune responses including differentiation of T cells (94), T cell responses were measured as well. Indeed, the CMA-induced Th2 and Th17 cell immune responses were downregulated by the specific AA diet (93). These effects of dietary AAs on effector T cells was accompanied by an upregulation of Treg cells in the small intestines of CMA mice. In another set of experiments using the same AA diet, the diet normalized the repetitive behavior of BTBRT(+)ltpr3(tf)/J mice, a frequently used murine model for ASD (93). This outcome was associated with an inhibition of the enhanced mTOR signaling pathway in the PFC of these mice, suggesting beneficial effects of the AA diet in both genetic and idiopathic forms of ASD (93).
The studies described above further establish mTOR activity to be a crucial factor in the gut-immune-brain axis playing a key role in the regulation of ASD-associated behavior. It has become clear that not only the effects of mTOR on the brain are important, but also the effects of mTOR concerning the regulation of immune responses and intestinal health. This warrants further investigation into the activity status of mTOR in peripheral blood mononuclear cells and intestinal biopsies of autistic patients. These data are needed to further substantiate mTOR as a therapeutic target or as biomarker in patients with ASD. Finally, based on the positive outcomes of an AA-based nutritional intervention on autistic behavior in mouse models for ASD, a proof of principle clinical study in ASD patients using this specific diet is warranted.
The Effects of Amino Acids on the Gut-Immune-Brain Axis in ASD Beyond mTOR
As described, specific AAs can modulate the activity of mTOR in a manner that might be beneficial for people with ASD. However, the potential of AAs to be beneficial for ASD is not limited to mTOR modulation. Numerous studies have shown that AAs can also exert beneficial effects on other components in the gut-immune-brain axis. Below, the interactions of AAs with the immune system and the gut microbiota (composition) will be discussed in relation to ASD.
The Potential Effects of Amino Acids on the Derailed Immune System Characteristic for ASD
Beyond targeting the ASD-enhanced mTOR signaling, AAs have been demonstrated to exhibit anti-inflammatory capabilities. As previously described, intestinal and systemic inflammation, as evaluated by a.o. higher levels of pro-inflammatory cytokines (e.g., IL-6, TNFα, and IL1β) are characteristic for people with ASD. In fact, inflammation is shown to induce ASD-associated behavior. Therefore, inhibition of systemic and/or intestinal inflammation might be beneficial for people diagnosed with ASD. Below, the immunomodulatory effects, mostly anti-inflammatory effects, of several AAs are described in relation to ASD.
Numerous studies investigated the immune modulatory functions of AAs in in vitro studies. Among these are studies that demonstrate anti-inflammatory effects of AAs on immune cells that might be affected in people with ASD. For instance, application of the BCAAs Leu, Ile and Val individually reduced the production of NO as well as mRNA and protein levels of the pro-inflammatory cytokine IL-6 in LPS-stimulated macrophages in vitro (95). Moreover, application of Leu, Ile, and Val individually or in combinations inhibited the acute degranulation and IL-6 production in antigen-IgE-activated mast cells, as previously mentioned (96). Whereas, increasing the availability of BCAAs has anti-inflammatory effects on specified immune cells, a decreased availability of the BCAAs leads to immune cell impairments. For instance, human lymphocytes cultured in medium containing Leu, Ile and Val at levels lower than the typical concentration in adult human plasma showed decreased ability to proliferate (97, 98). Not only in vitro, but also in vivo experiments demonstrate the importance of an adequate availability of BCAAs for normal immune cell functioning. For example, reducing the levels of Leu, Ile, and Val by 50% in an otherwise normal mice diet increased the susceptibility of mice to salmonella infections, potentially due to an impaired antibody production (99). These mice also showed a lowered number of spleen cells, which might be indicative of a decreased lymphocyte proliferation in vivo (99). Interestingly, Novarino et al. identified inactivating mutations in the gene branched chain keto-acid dehydrogenase kinase (BCKDK) in several ASD patients (100). Loss of BCKDK function resulted in hypercatabolism of Leu, Ile and Val, leading to abnormally low levels of these BCAAs in serum and in the brain (100). Knowing the importance of adequate BCAA availability for normal immune cell functioning, these mutations might contribute to the immune impairments observed in a subgroup of individuals with ASD.
In addition to the observed anti-inflammatory effects of the BCAAs in vitro and in mouse models, this group of AAs also has demonstrated anti-inflammatory effects in immune compromised humans. For example, in cirrhotic patients, daily supplementation of Leu, Ile and Val improved innate immune cell functions including the phagocytic function of neutrophils and natural killer activity of lymphocytes, which are processes that are also impaired in people with ASD (17, 101, 102). Also, in patients with rectal cancer, infusing a solution enriched in Leu, Ile and Val led to an increase in the number of CD4+ (Th) cells in blood, and led to an increased ratio of CD4+/CD8+ (cytotoxic T) cells in the blood (103). Studies have demonstrated that autistic individuals have fewer CD4+ cells and a lower CD4+/CD8+ cell ratio in blood, indicating immune impairments (104–106). Interestingly, Abd El-Aziz et al. showed a negative correlation between the CD4+/CD8+ cell ratio in blood of individuals with ASD and the severity of autistic behavior. Thus, factors like Leu, Ile and Val that increase the ratio of CD4+/CD8+ cells might provide therapeutic benefits for ASD patients (104).
Besides their modulatory capacities on peripheral immune cells, the BCAAs also affect microglial cells, the immune cells of the brain. Culturing rat microglial cells in a medium enriched with these BCAAs induced a more anti-inflammatory state of the microglial cells after LPS stimulation (107). This was supported by a decreased microglial production of IL-1β, TNFα, and inducible nitric-oxide synthase (iNOS), as well as an increased production of IL-10, both at the level of mRNA and at the protein level (107). Moreover, microglial phagocytic capacity, which is critical for normal brain functioning and is impaired in individuals with ASD (108), was stimulated by the presence of high levels of the BCAAs (107). However, neuroprotective functions of microglial cells were impaired in the presence of high levels of Leu, Ile and Val, as represented by a decreased production of the neuroprotective factor Insulin-like growth factor 1 (IGF-1) (107). The latter observation is in line with the possible detrimental effects of mTOR-hyperactivation.
Alongside the BCAAs, the essential AAs Thr, Lys, and His also have immunomodulating capacities, potentially via modulation of mTOR signaling (93). Of these AAs, Thr has been most widely associated with immunomodulation in vivo. Animal studies have demonstrated that Thr is critical for intestinal barrier and immune function and can improve intestinal epithelial integrity in inflammatory conditions where the gut barrier is impaired, as is the case in ASD (109). For instance, in various rat models of colitis, a Thr-enriched diet was shown to restore mucus synthesis and normalize the gut microbiota, thereby improving intestinal function (110, 111). Studies in animals and humans also suggest an increased requirement of Thr by the intestines in inflammatory conditions in order to maintain intestinal barrier function (112, 113). Although less widely studied, the AA His also interacts with the immune system. Apart from its use for the generation of histamine, a key molecule involved in immune responses, His exhibits anti-inflammatory effects on a variety of immune cells. For instance, in vitro studies show that supplementation of His suppressed IL-8 secretion in TNFα-activated human epithelial cells, PBMCs and monocytes (114, 115). The immunomodulating ability of His is also demonstrated in vivo, as dietary His improved murine colitis by inhibiting the production of pro-inflammatory cytokines by macrophages (116). Studies examining the immunomodulatory effects of Lys are limited. However, dietary deficiency of Lys has been shown to limit lymphocyte proliferation and induces a pro-inflammatory state, represented by increased levels of pro-inflammatory cytokines and NO in the kidney, liver and spleen of piglets (117). Taken together, data from both in vitro and in vivo experiments suggest that there is a potential for the AAs Thr, Lys, and His to ameliorate the compromised gut-immune-brain axis in ASD.
In addition to the AAs that are demonstrated to interact with mTOR, several other AAs also have anti-inflammatory capabilities, in particular glycine (Gly), glutamine (Gln) and glutamate (Glu). In vitro studies demonstrated that supplementation of Gly protects intestinal epithelial cells against inflammatory oxidative stress (118), and reduces pro-inflammatory cytokine production while enhancing IL-10 expression of LPS-stimulated monocytes (119). The capacity of Gly to exert anti-inflammatory effects is further supported by in vivo studies using a variety of animal immune models. For instance, oral intake of Gly reduced TNFα production and improved the survival rate of LPS-injected rats (120), reduced inflammation and oxidative stress in a mouse model of cancer cachexia (121) and inhibited the onset of CMA in mice (122). As the pro-inflammatory, allergic-like status of the intestines in people with ASD might play a role in the induction of autistic-like behavior, it can be speculated that dietary Gly supplementation might have therapeutic potential for individuals with ASD.
The AAs Gln and Glu are related to each other, both in terms of structure and their immunomodulatory capabilities. Both Gln and Glu are critical for intestinal growth and functions and are shown to reduce intestinal hyperpermeability both in vitro and in vivo (123–125). Remarkably, plasma levels of Gln are reported to be lower in patients with ASD as compared to healthy individuals (126). The reduced bioavailability of Gln might be involved in the mucosal barrier impairments observed in individuals with ASD. This is supported by studies demonstrating that low levels of serum Gln correlate with intestinal barrier disruption and inflammation in children (127, 128). Besides its involvement in intestinal barrier function, Gln is also widely known as an anti-inflammatory agent, likely via inhibition of the activation of nuclear factor kappa B (NF-κB) and signal transducers and activators of transcription (STAT) (129). In turn, this inhibition leads to suppression of the production of inflammatory cytokines such as IL-6, TNFα and IL-8 as shown for various immune cells in vitro, in animal immune models and in immune-compromised human (129–131). As such, Gln is proposed as candidate for treating inflammatory disorders. Anti-inflammatory effects of Glu include the inhibition of Th2 cells, the stimulation of the production of regulatory cytokine IL-10 by Treg cells and the stimulation of Treg cell development via modulation of the cytokine expression by dendritic cells (132, 133).
Besides their involvement in inflammatory immune responses, Gly and Glu are also neuroactive AAs. Glu is the primary excitatory neurotransmitter of the brain, which is stored in the form of Gln until it is transferred to presynaptic terminals and converted back to Glu (134). Normally, Glu has a protective effect on cognitive function and neural plasticity. However, excessive levels of Glu may be neurotoxic and may play a role in neuroinflammation events in the pathogenesis of ASD (135). Accordingly, multiple studies report higher levels of Glu in serum, plasma and the brain of people with ASD as compared to healthy controls (136–138). In contrast, levels of Gly, a major inhibitory neurotransmitter, are found to be unchanged in patients with ASD (126). The imbalance between Gly and Gln might drive an imbalance in inhibitory and excitatory neurotransmitters, which is indicated to lead to excessive neuroinflammation (137).
As discussed, specific AAs can modify the functions of the immune system in a way that might be beneficial for individuals with ASD. Conversely, the derailed immune system observed in ASD can also modulate the bioavailability of specific AAs, and thereby drive the pathogenesis of ASD. This has been demonstrated most clearly for tryptophan (Trp), of which plasma levels are consistently shown to be lower in ASD patients (139–141). Apart from being a precursor for the neurotransmitter serotonin, Trp is extensively metabolized in the kynurenine pathway (142). This pathway produces several immunomodulatory and neuroactive compounds, examples of which include kynurenine (142) and quinolinic acid (143), respectively. In pro-inflammatory conditions, like ASD, the activation of the kynurenine pathway is enhanced (144), leading to abnormal production of metabolites with neurotoxic effects (144, 145). Furthermore, the kynurenine pathway produces metabolites that induce apoptosis in Th1 cells but not in Th2 cells, suggesting that an increased activation of this pathway favors Th2 polarization, which is characteristic for ASD (146). Finally, aberrant activation of the kynurenine pathway in ASD also diverts Trp from the serotonin synthesis route (144, 147, 148). Psychological complications characteristic for a.o. ASD patients may originate from serotonin deficiency mediated by the depletion of Trp following kynurenine pathway activation (139, 148), which is also reported in a murine model for ASD (149, 150). Whereas, aberrant Trp metabolism might induce neurotoxicity and a Th2-type immune status, Trp can also act as an anti-inflammatory agent. For instance, dietary supplementation of Trp in a mouse and piglet model for colitis reduced inflammation (151, 152), whereas mice fed a low-Trp diet became increasingly susceptible to chemically induced inflammation (153). Promising effects of a multi-nutrient diet containing high Trp on disturbed behavior and reduced intestinal and CNS serotonin levels are reported in a murine model for ASD (96). Whether dietary supplementation of Trp has therapeutic potential for ASD patients remains open to speculation: it might further drive abnormal activation of the kynurenine pathway, however, it could also provide benefits by reducing inflammation and normalizing serotonin synthesis.
The Interaction Between Amino Acids and the Gut Microbiome in Relation to ASD
Accumulating evidence has demonstrated a bidirectional communication between the brain and the gut, with the intestinal microbiota as a key factor in both health and disease (154, 155). The microbiota can affect cognition and behavior, as has been demonstrated in an increasing number of studies (156–158). Modification of the microbiota composition or absence of the microbiota impacts the hypothalamic-pituitary-adrenal (HPA) axis, the immune system and behavior (158). The importance of gut microbiota in early life and brain development is demonstrated by animal studies showing that maternal separation of neonates does not only lead to a dysbiotic state of the microbiota that persists into adulthood, but also results in long-term cognitive and behavioral deficits (159). Nevertheless, the mechanistic link between the gut microbiota, gut immune homeostasis, and brain functioning remains poorly understood. A variety of mechanisms including immune, hormonal and neural pathways are likely to be involved and may depend on the nature of the microbiota dysbiosis. Also for ASD, the microbiome-gut-immune-brain axis is suggested to be important as profound changes in the microbial composition and activity have been reported (160). Below, we describe the possible interaction between AAs and the gut microbiota in perspective of ASD.
Over the last decades extensive studies have revealed that the gut microbiota composition plays an important role in the metabolism and recycling of nitrogen-containing compounds (161, 162). One of the major nitrogenous compounds utilized by gut bacteria are AAs. AAs derived from either the host or from food enter the gut and are metabolized by gut bacteria into a wide variety of products (163). Hence, it can be speculated that the gut microbiota regulates the AA pool and composition that is available to the host. This is supported by a study demonstrating that gut bacteria alter the AA distribution in the gastrointestinal tract (164). Alterations in AA availability may lead to changes in signaling pathways that are sensitive to AAs, including the mTOR signaling and inflammatory pathways (77, 165). For instance, studies demonstrated that people with ASD have lower BCAA levels in their plasma, urine and cerebrospinal fluid (141, 166, 167). A deficiency of any of the BCAAs is shown to cause immune cell impairments in various animal models, leading to a more pro-inflammatory immune status (168), which is also observed in people with ASD. A possible explanation for the abnormal levels of BCAAs might be an increased conversion of these AAs by gut Proteobacteria, as these are among the most extensive BCAA-fermenting bacteria (169) and are shown to be more abundant in people with ASD (170–172).
Gut bacteria do not only alter AA availability, but they also play a role in the availability of AA-derived metabolites. For instance, levels of Thr are shown to be decreased in patients with ASD (141, 167, 173). Gut bacteria use Thr for a.o. the production of short-chain fatty acids (SCFAs), mainly propionate (163, 174). Studies have revealed an increased abundance of propionate in people with ASD (175, 176). In fact, elevated propionate production is postulated to be involved in the pathogenesis of ASD, as this SCFA is shown to cross the blood-brain barrier and is able to induce ASD-like behavior in adult rodents, possibly via activation of microglia (177–179). The gut microbiome also has a role in the regulation Trp metabolism (180, 181). Deviations in either endogenous or bacterial Trp metabolism have been associated with a variety of immune-related disorders, including ASD (182, 183). For instance, a recent study demonstrated a significant reduction of serotonin bioavailability in the intestines of a mouse models for ASD (96, 149). This reduction was accompanied by a down-regulation of the gene Tph1, indicating a lower production of serotonin from dietary Trp (149). Interestingly, serotonin production from Trp was positively associated with the abundance of the Blautia bacteria present in the gut. In both mouse models of ASD and in humans with ASD, the abundance of Blautia bacteria is reported to be lower compared to healthy controls (149, 184). This change in the microbiota might underlie the abnormal Trp-metabolism and serotonin bioavailability that is frequently observed in ASD patients as well as in in vivo models for ASD and thus may drive ASD pathogenesis.
As discussed, the gut microbiota influences the bioavailability of AAs and their metabolites. Vice versa, the availability of AAs can also influence the microbiota composition. For instance, several studies have reported that the gut microbiota of people with ASD as well as in murine ASD models is characterized by a significantly higher ratio of Firmicutes to Bacteroidetes, mainly due to a decrease in Bacteroidetes (171, 185, 186). The ratio of Firmicutes to Bacteroidetes, which are the two most abundant bacterial phyla in human, is considered of significant relevance in human health (187). An increased Firmicutes/Bacteroidetes ratio might be involved in inducing inflammation, as this is observed in several inflammatory conditions and as this ratio is shown to be positively associated with dysregulated humoral and cellular immunity (188, 189). Interestingly, dietary supplementation of arginine (Arg) in healthy mice decreased the Firmicutes to Bacteroidetes ratio in the small intestine, mainly due to an increase in Bacteroidetes (190). Similarly, dietary supplementation of Gln decreased the Firmicutes/Bacteroidetes ratio in sows (191). Whether modulation of Gln and Arg intake can restore the aberrant Firmicutes/Bacteroidetes ratio observed in ASD patients, and subsequently improve their immune status remains to be examined.
Furthermore, several studies have reported an increase in the abundance of Proteobacteria in people with ASD (170–172). Proteobacteria are often found to be increased in inflammatory conditions such as colitis and inflammatory bowel disease and have been identified as a marker for microbiota instability and gut inflammation (192, 193). Supplementation of BCAAs was shown to largely reduce the abundance of Proteobacteria in mice, accompanied by lower concentrations of inflammatory marker LPS-binding protein (LBP) in serum (194), which has been shown to be elevated in ASD patients (195). In addition, BCAA supplementation also reduced the Firmicutes/Bacteroidetes ratio in middle-aged mice (194). However, whether BCAA supplementation is able to restore the abnormal gut microbiota in ASD, and which underlying mechanisms are involved remains to be further investigated.
In Table 1, an overview is presented of the complex roles of AAs described in this review regarding the microbiome-gut-immune-brain axis in ASD. Besides behavioral deficits, people with ASD are characterized by systemic inflammation, gastrointestinal immune-related disturbances and changes in the gut microbiota composition. Moreover, differences in levels of specific AAs in various body compartments, including the intestinal tract, blood, urine and brain have been reported in patients with ASD, as well as in rodent models for ASD. This review described that specific AAs can modulate the intestinal epithelial immune barrier and are able to tune the mucosal immune system, possibly through influencing the mTOR pathway in immune cells. Moreover, specific AAs can influence neuroinflammatory processes and can target the aberrant mTOR signaling in the brain, thereby influencing neuronal activity and disturbed behavior associated with ASD. Finally, though limited reports are available, dietary AAs can influence the changed intestinal microbiota composition and activity of people with ASD. Figure 4 shows a graphical overview of the different targets for dietary AAs in ASD. Taken together, this review creates more insight in the complex pathogenic relevance of the microbiome-gut-immune-brain axis in ASD and warrants additional research into the opportunities for AA-based nutritional interventions as treatment for ASD in the system medicine approach.
Table 1. Overview of the complex roles of amino acids in the microbiome-gut-immune-brain axis in ASD.
Figure 4. Schematic representation of the possible targets for dietary amino acids in the impaired gut-microbiome-immune-brain axis in ASD.
All authors listed have made a substantial, direct and intellectual contribution to the work, and approved it for publication.
This review was funded by the Nutricia-Utrecht University alliance.
Conflict of Interest Statement
JvS, JG, JvB, AH are current employees of Danone Nutricia Research.
The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
5. Hansen SN, Schendel DE, Parner ET. Explaining the increase in the prevalence of autism spectrum disorders: the proportion attributable to changes in reporting practices. JAMA Pediatr. (2015) 169:56–62. doi: 10.1001/jamapediatrics.2014.1893
6. Kim YS, Leventhal BL, Koh YJ, Fombonne E, Laska E, Lim EC, et al. Prevalence of autism spectrum disorders in a total population sample. Am J Psychiatry. (2011) 168:904–12. doi: 10.1176/appi.ajp.2011.10101532
7. Lyall K, Croen L, Daniels J, Fallin MD, Ladd-Acosta C, Lee BK, et al. The changing epidemiology of autism spectrum disorders. Annu Rev Public Health. (2017) 38:81–102. doi: 10.1146/annurev-publhealth-031816-044318
18. Morgan JT, Chana G, Pardo CA, Achim C, Semendeferi K, Buckwalter J, et al. Microglial activation and increased microglial density observed in the dorsolateral prefrontal cortex in autism. Biol Psychiatry. (2010) 68:368–76. doi: 10.1016/j.biopsych.2010.05.024
20. Atladottir HO, Pedersen MG, Thorsen P, Mortensen PB, Deleuran B, Eaton WW, et al. Association of family history of autoimmune diseases and autism spectrum disorders. Pediatrics. (2009) 124:687–94. doi: 10.1542/peds.2008-2445
21. Molloy CA, Morrow AL, Meinzen-Derr J, Schleifer K, Dienger K, Manning-Courtney P, et al. Elevated cytokine levels in children with autism spectrum disorder. J Neuroimmunol. (2006) 172:198–205. doi: 10.1016/j.jneuroim.2005.11.007
23. Odell D, Maciulis A, Cutler A, Warren L, McMahon WM, Coon H, et al. Confirmation of the association of the c4b null allelle in autism. Hum Immunol. (2005) 66:140–5. doi: 10.1016/j.humimm.2004.11.002
24. Ashwood P, Enstrom A, Krakowiak P, Hertz-Picciotto I, Hansen RL, Croen LA, et al. Decreased transforming growth factor beta1 in autism: a potential link between immune dysregulation and impairment in clinical behavioral outcomes. J Neuroimmunol. (2008) 204:149–53. doi: 10.1016/j.jneuroim.2008.07.006
25. Enstrom A, Onore C, Hertz-Picciotto I, Hansen R, Croen L, Van de Water J, et al. Detection of il-17 and il-23 in plasma samples of children with autism. Am J Biochem Biotechnol. (2008) 4:114–20. doi: 10.3844/ajbbsp.2008.114.120
26. Okada K, Hashimoto K, Iwata Y, Nakamura K, Tsujii M, Tsuchiya KJ, et al. Decreased serum levels of transforming growth factor-beta1 in patients with autism. Prog Neuropsychopharmacol Biol Psychiatry. (2007) 31:187–90. doi: 10.1016/j.pnpbp.2006.08.020
27. Hashim H, Abdelrahman H, Mohammed D, Karam R. Association between plasma levels of transforming growth factor-β1, il-23 and il-17 and the severity of autism in egyptian children. Res Autism Spectr Disord. (2013) 7:199–204. doi: 10.1016/j.rasd.2012.08.007
28. Mostafa GA, Al Shehab A, Fouad NR. Frequency of cd4+cd25high regulatory t cells in the peripheral blood of egyptian children with autism. J Child Neurol. (2010) 25:328–35. doi: 10.1177/0883073809339393
29. Shevach EM, Tran DQ, Davidson TS, Andersson J. The critical contribution of tgf-beta to the induction of foxp3 expression and regulatory t cell function. Eur J Immunol. (2008) 38:915–7. doi: 10.1002/eji.200738111
32. Ashwood P, Krakowiak P, Hertz-Picciotto I, Hansen R, Pessah I, Van de Water J. Elevated plasma cytokines in autism spectrum disorders provide evidence of immune dysfunction and are associated with impaired behavioral outcome. Brain Behav Immun. (2011) 25:40–5. doi: 10.1016/j.bbi.2010.08.003
33. Ashwood P, Krakowiak P, Hertz-Picciotto I, Hansen R, Pessah IN, Van de Water J. Associations of impaired behaviors with elevated plasma chemokines in autism spectrum disorders. J Neuroimmunol. (2011) 232:196–9. doi: 10.1016/j.jneuroim.2010.10.025
34. Leigh LY, Spergel JM. An in-depth characterization of a large cohort of adults patients with eosinophilic esophagitis. Ann Allergy Asthma Immunol. (2018) 122:65–72.e1. doi: 10.1016/j.anai.2018.09.452
35. Theoharides TC, Tsilioni I, Patel AB, Doyle R. Atopic diseases and inflammation of the brain in the pathogenesis of autism spectrum disorders. Transl Psychiatry. (2016) 6:e844. doi: 10.1038/tp.2016.77
36. NIAID-Sponsored Expert Panel, Boyce JA, Assa'ad A, Burks AW, Jones SM, Sampson HA, et al. Guidelines for the diagnosis and management of food allergy in the united states: report of the niaid-sponsored expert panel. J Allergy Clin Immunol. (2010) 126:S1–58. doi: 10.1016/j.jaci.2010.10.007
37. Kobayashi T, Iijima K, Dent AL, Kita H. Follicular helper t cells mediate ige antibody response to airborne allergens. J Allergy Clin Immunol. (2017) 139:300–313.e307. doi: 10.1016/j.jaci.2016.04.021
39. de Theije CG, Wu J, da Silva SL, Kamphuis PJ, Garssen J, Korte SM, et al. Pathways underlying the gut-to-brain connection in autism spectrum disorders as future targets for disease management. Eur J Pharmacol. (2011) 668 (Suppl. 1):S70–80. doi: 10.1016/j.ejphar.2011.07.013
40. Gurney JG, McPheeters ML, Davis MM. Parental report of health conditions and health care use among children with and without autism: National survey of children's health. Arch Pediatr Adolesc Med. (2006) 160:825–30. doi: 10.1001/archpedi.160.8.825
41. Lyall K, Van de Water J, Ashwood P, Hertz-Picciotto I. Asthma and allergies in children with autism spectrum disorders: Results from the charge study. Autism Res. (2015) 8:567–74. doi: 10.1002/aur.1471
42. Sanctuary MR, Kain JN, Angkustsiri K, German JB. Dietary considerations in autism spectrum disorders: the potential role of protein digestion and microbial putrefaction in the gut-brain axis. Front Nutr. (2018) 5:40. doi: 10.3389/fnut.2018.00040
44. de Theije CG, Wu J, Koelink PJ, Korte-Bouws GA, Borre Y, Kas MJ, et al. Autistic-like behavioural and neurochemical changes in a mouse model of food allergy. Behav Brain Res. (2014) 261:265–74. doi: 10.1016/j.bbr.2013.12.008
45. Dalton KM, Nacewicz BM, Johnstone T, Schaefer HS, Gernsbacher MA, Goldsmith HH, et al. Gaze fixation and the neural circuitry of face processing in autism. Nat Neurosci. (2005) 8:519–26. doi: 10.1038/nn1421
46. Belmonte MK, Gomot M, Baron-Cohen S. Visual attention in autism families: 'Unaffected' sibs share atypical frontal activation. J Child Psychol Psychiatry. (2010) 51:259–76. doi: 10.1111/j.1469-7610.2009.02153.x
47. Hara Y, Takuma K, Takano E, Katashiba K, Taruta A, Higashino K, et al. Reduced prefrontal dopaminergic activity in valproic acid-treated mouse autism model. Behav Brain Res. (2015) 289:39–47. doi: 10.1016/j.bbr.2015.04.022
52. Rozniecki JJ, Dimitriadou V, Lambracht-Hall M, Pang X, Theoharides TC. Morphological and functional demonstration of rat dura mater mast cell-neuron interactions in vitro and in vivo. Brain Res. (1999) 849:1–15. doi: 10.1016/S0006-8993(99)01855-7
56. de Magistris L, Familiari V, Pascotto A, Sapone A, Frolli A, Iardino P, et al. Alterations of the intestinal barrier in patients with autism spectrum disorders and in their first-degree relatives. J Pediatr Gastroenterol Nutr. (2010) 51:418–24. doi: 10.1097/MPG.0b013e3181dcc4a5
57. Konig J, Wells J, Cani PD, Garcia-Rodenas CL, MacDonald T, Mercenier A, et al. Human intestinal barrier function in health and disease. Clin Transl Gastroenterol. (2016) 7:e196. doi: 10.1038/ctg.2016.54
58. Hsiao EY, McBride SW, Hsien S, Sharon G, Hyde ER, McCue T, et al. Microbiota modulate behavioral and physiological abnormalities associated with neurodevelopmental disorders. Cell. (2013) 155:1451–63. doi: 10.1016/j.cell.2013.11.024
59. Costa RM, Federov NB, Kogan JH, Murphy GG, Stern J, Ohno M, et al. Mechanism for the learning deficits in a mouse model of neurofibromatosis type 1. Nature. (2002) 415:526–30. doi: 10.1038/nature711
60. Zhou J, Blundell J, Ogawa S, Kwon CH, Zhang W, Sinton C, et al. Pharmacological inhibition of mtorc1 suppresses anatomical, cellular, and behavioral abnormalities in neural-specific pten knock-out mice. J Neurosci. (2009) 29:1773–83. doi: 10.1523/JNEUROSCI.5685-08.2009
61. Goorden SM, van Woerden GM, van der Weerd L, Cheadle JP, Elgersma Y. Cognitive deficits in tsc1+/- mice in the absence of cerebral lesions and seizures. Ann Neurol. (2007) 62:648–55. doi: 10.1002/ana.21317
68. Delgoffe GM, Pollizzi KN, Waickman AT, Heikamp E, Meyers DJ, Horton MR, et al. The kinase mtor regulates the differentiation of helper t cells through the selective activation of signaling by mtorc1 and mtorc2. Nat Immunol. (2011) 12:295–303. doi: 10.1038/ni.2005
70. Delgoffe GM, Kole TP, Zheng Y, Zarek PE, Matthews KL, Xiao B, et al. The mtor kinase differentially regulates effector and regulatory t cell lineage commitment. Immunity. (2009) 30:832–44. doi: 10.1016/j.immuni.2009.04.014
71. Deason K, Troutman TD, Jain A, Challa DK, Mandraju R, Brewer T, et al. Bcap links il-1r to the pi3k-mtor pathway and regulates pathogenic th17 cell differentiation. J Exp Med. (2018) 215:2413–28. doi: 10.1084/jem.20171810
72. Lee K, Gudapati P, Dragovic S, Spencer C, Joyce S, Killeen N, et al. Mammalian target of rapamycin protein complex 2 regulates differentiation of th1 and th2 cell subsets via distinct signaling pathways. Immunity. (2010) 32:743–53. doi: 10.1016/j.immuni.2010.06.002
73. Xu G, Xia J, Hua X, Zhou H, Yu C, Liu Z, et al. Activated mammalian target of rapamycin is associated with t regulatory cell insufficiency in nasal polyps. Respir Res. (2009) 10:13. doi: 10.1186/1465-9921-10-13
75. Pott J, Kabat AM, Maloy KJ. Intestinal epithelial cell autophagy is required to protect against tnf-induced apoptosis during chronic colitis in mice. Cell Host Microbe. (2018) 23:191–202.e194. doi: 10.1016/j.chom.2017.12.017
76. Magdalon J, Sánchez-Sánchez SM, Griesi-Oliveira K, Sertié AL. Dysfunctional mtorc1 signaling: A convergent mechanism between syndromic and nonsyndromic forms of autism spectrum disorder? Int J Mol. Sci. (2017) 18:659. doi: 10.3390/ijms18030659
78. Burket JA, Benson AD, Tang AH, Deutsch SI. Rapamycin improves sociability in the btbr t(+)itpr3(tf)/j mouse model of autism spectrum disorders. Brain Res Bull. (2014) 100:70–5. doi: 10.1016/j.brainresbull.2013.11.005
79. Chi OZ, Wu CC, Liu X, Rah KH, Jacinto E, Weiss HR. Restoration of normal cerebral oxygen consumption with rapamycin treatment in a rat model of autism-tuberous sclerosis. Neuromolecular Med. (2015) 17:305–13. doi: 10.1007/s12017-015-8359-5
80. Steinmetz AB, Stern SA, Kohtz AS, Descalzi G, Alberini CM. Insulin-like growth factor ii targets the mtor pathway to reverse autism-like phenotypes in mice. J Neurosci. (2018) 38:1015. doi: 10.1523/JNEUROSCI.2010-17.2017
82. Wu J, de Theije CG, da Silva SL, van der Horst H, Reinders MT, Broersen LM, et al. Mtor plays an important role in cow's milk allergy-associated behavioral and immunological deficits. Neuropharmacology. (2015) 97:220–32. doi: 10.1016/j.neuropharm.2015.04.035
83. Fischer KE, Gelfond JAL, Soto VY, Han C, Someya S, Richardson A, et al. Health effects of long-term rapamycin treatment: the impact on mouse health of enteric rapamycin treatment from four months of age throughout life. PLoS ONE. (2015) 10:e0126644. doi: 10.1371/journal.pone.0126644
86. Shah OJ, Anthony JC, Kimball SR, Jefferson LS. 4e-bp1 and s6k1: translational integration sites for nutritional and hormonal information in muscle. American journal of physiology Endocrinology and metabolism. (2000) 279:E715–729. doi: 10.1152/ajpendo.2000.279.4.E715
93. Wu J, de Theije CGM, da Silva SL, Abbring S, van der Horst H, Broersen LM, et al. Dietary interventions that reduce mtor activity rescue autistic-like behavioral deficits in mice. Brain Behav Immun. (2017) 59:273–87. doi: 10.1016/j.bbi.2016.09.016
95. Lee JH, Park E, Jin HJ. Anti-inflammatory and anti-genotoxic activity of branched chain amino acids (bcaa) in lipopolysaccharide (lps) stimulated raw 264.7 macrophages. Food Sci Biotechnol. (2017) 26:1371–7. doi: 10.1007/s10068-017-0165-4
98. Skaper SD, Molden DP, Seegmiller JE. Maple syrup urine disease: branched-chain amino acid concentrations and metabolism in cultured human lymphoblasts. Biochem Genet. (1976) 14:527–39. doi: 10.1007/BF00485832
99. Petro TM, Bhattacharjee JK. Effect of dietary essential amino acid limitations upon the susceptibility to salmonella typhimurium and the effect upon humoral and cellular immune responses in mice. Infect Immun. (1981) 32:251–9.
100. Novarino G, El-Fishawy P, Kayserili H, Meguid NA, Scott EM, Schroth J, et al. Mutations in bckd-kinase lead to a potentially treatable form of autism with epilepsy. Science. (2012) 338:394–7. doi: 10.1126/science.1224631
101. Nakamura I. (2014). Impairment of innate immune responses in cirrhotic patients and treatment by branched-chain amino acids. World J Gastroenterol. (2014) 20:7298–305. doi: 10.3748/wjg.v20.i23.7298
102. Vojdani A, Mumper E, Granpeesheh D, Mielke L, Traver D, Bock K, et al. Low natural killer cell cytotoxic activity in autism: the role of glutathione, il-2 and il-15. J Neuroimmunol. (2008) 205:148–54. doi: 10.1016/j.jneuroim.2008.09.005
103. Zhang HW, Wang F, Wei-zhong L, Meng-bin JG, Guan C. The effects of bcaa-enriched amino acid solution on immune function and protein metabolism in postoperative patients with rectal cancer. Parenter Enteral Nutr. (2007) 2:009. Available online at: http://en.cnki.com.cn/Article_en/CJFDTOTAL-CWCN200702009.htm
104. Abd El-Aziz SA, Alm El-Din RA. Cellular-mediated and humoral immunity in children with autism. Egypt J Pediatr Allergy Immunol. (2012) 10:25–32. Available online at: https://www.ajol.info/index.php/ejpai/article/view/108274
105. Bjorklund G, Saad K, Chirumbolo S, Kern JK, Geier DA, Geier MR, et al. Immune dysfunction and neuroinflammation in autism spectrum disorder. Acta Neurobiol Exp. (2016) 76:257–68. doi: 10.21307/ane-2017-025
106. Bradstreet JJ, Sych N, Antonucci N, Klunnik M, Ivankova O, Matyashchuk I, et al. Efficacy of fetal stem cell transplantation in autism spectrum disorders: An open-labeled pilot study. Cell Transplant. (2014) 23 (Suppl. 1):S105–12. doi: 10.3727/096368914X684916
107. De Simone R, Vissicchio F, Mingarelli C, De Nuccio C, Visentin S, Ajmone-Cat MA, et al. Branched-chain amino acids influence the immune properties of microglial cells and their responsiveness to pro-inflammatory signals. Biochim Biophys Acta. (2013) 1832:650–9. doi: 10.1016/j.bbadis.2013.02.001
108. Kim HJ, Cho MH, Shim WH, Kim JK, Jeon EY, Kim DH, et al. Deficient autophagy in microglia impairs synaptic pruning and causes social behavioral defects. Mol Psychiatry. (2017) 22:1576–84. doi: 10.1038/mp.2016.103
110. Faure M, Mettraux C, Moennoz D, Godin JP, Vuichoud J, Rochat F, et al. Specific amino acids increase mucin synthesis and microbiota in dextran sulfate sodium-treated rats. J Nutr. (2006) 136:1558–64. doi: 10.1093/jn/136.6.1558
111. Liu X, Beaumont M, Walker F, Chaumontet C, Andriamihaja M, Matsumoto H, et al. Beneficial effects of an amino acid mixture on colonic mucosal healing in rats. Inflamm Bowel Dis. (2013) 19:2895–905. doi: 10.1097/01.MIB.0000435849.17263.c5
112. Dawson P, Filipe MI. Uptake of (3h)thr in human colonic mucosa associated with carcinoma: an autoradiographic analysis at the ultrastructural level. Histocheml J. (1982) 14:385–401. doi: 10.1007/BF01011851
113. Remond D, Buffiere C, Godin JP, Mirand PP, Obled C, Papet I, et al. Intestinal inflammation increases gastrointestinal threonine uptake and mucin synthesis in enterally fed minipigs. J Nutr. (2009) 139:720–6. doi: 10.3945/jn.108.101675
114. Hasegawa S, Ichiyama T, Sonaka I, Ohsaki A, Hirano R, Haneda Y, et al. Amino acids exhibit anti-inflammatory effects in human monocytic leukemia cell line, thp-1 cells. Inflamm Res. (2011) 60:1013–9. doi: 10.1007/s00011-011-0362-1
115. Son DO, Satsu H, Shimizu M. Histidine inhibits oxidative stress- and tnf-alpha-induced interleukin-8 secretion in intestinal epithelial cells. FEBS Lett. (2005) 579:4671–7. doi: 10.1016/j.febslet.2005.07.038
116. Andou A, Hisamatsu T, Okamoto S, Chinen H, Kamada N, Kobayashi T, et al. Dietary histidine ameliorates murine colitis by inhibition of proinflammatory cytokine production from macrophages. Gastroenterology. (2009) 136:564–574.e562. doi: 10.1053/j.gastro.2008.09.062
118. Howard A, Tahir I, Javed S, Waring SM, Ford D, Hirst BH. Glycine transporter glyt1 is essential for glycine-mediated protection of human intestinal epithelial cells against oxidative damage. J Physiol. (2010) 588:995–1009. doi: 10.1113/jphysiol.2009.186262
119. Spittler A, Reissner CM, Oehler R, Gornikiewicz A, Gruenberger T, Manhart N, et al. Immunomodulatory effects of glycine on lps-treated monocytes: reduced tnf-alpha production and accelerated il-10 expression. FASEB J. (1999) 13:563–71. doi: 10.1096/fasebj.13.3.563
121. Ham DJ, Murphy KT, Chee A, Lynch GS, Koopman R. Glycine administration attenuates skeletal muscle wasting in a mouse model of cancer cachexia. Clin Nutr. (2014) 33:448–58. doi: 10.1016/j.clnu.2013.06.013
122. van Bergenhenegouwen J, Braber S, Loonstra R, Buurman N, Rutten L, Knipping K, et al. Oral exposure to the free amino acid glycine inhibits the onset of cow's milk allergy. Nutr Res. (2018) 58:95–105. doi: 10.1016/j.nutres.2018.07.005
123. Ewaschuk JB, Murdoch GK, Johnson IR, Madsen KL, Field CJ. Glutamine supplementation improves intestinal barrier function in a weaned piglet model of escherichia coli infection. Br J Nutr. (2011) 106:870–7. doi: 10.1017/S0007114511001152
124. Vermeulen MA, de Jong J, Vaessen MJ, van Leeuwen PA, Houdijk AP. Glutamate reduces experimental intestinal hyperpermeability and facilitates glutamine support of gut integrity. World J Gastroenterol. (2011) 17:1569–73. doi: 10.3748/wjg.v17.i12.1569
125. Wu X, Zhang Y, Liu Z, Li TJ, Yin YL. Effects of oral supplementation with glutamate or combination of glutamate and n-carbamylglutamate on intestinal mucosa morphology and epithelium cell proliferation in weanling piglets. J Anim Sci. (2012) 90 (Suppl. 4):337–9. doi: 10.2527/jas.53752
126. Zheng HF, Wang WQ, Li XM, Rauw G, Baker GB. Body fluid levels of neuroactive amino acids in autism spectrum disorders: a review of the literature. Amino Acids. (2017) 49:57–65. doi: 10.1007/s00726-016-2332-y
127. Guerrant RL, Oria RB, Moore SR, Oria MO, Lima AA. Malnutrition as an enteric infectious disease with long-term effects on child development. Nutr Rev. (2008) 66:487–505. doi: 10.1111/j.1753-4887.2008.00082.x
128. Lima NL, Soares AM, Mota RM, Monteiro HS, Guerrant RL, Lima AA. Wasting and intestinal barrier function in children taking alanyl-glutamine-supplemented enteral formula. J Pediatr Gastroenterol Nutr. (2007) 44:365–74. doi: 10.1097/MPG.0b013e31802eecdd
131. Lechowski S, Feilhauer K, Staib L, Coeffier M, Bischoff SC, Lorentz A. Combined arginine and glutamine decrease release of de novo synthesized leukotrienes and expression of proinflammatory cytokines in activated human intestinal mast cells. Eur J Nutr. (2013) 52:505–12. doi: 10.1007/s00394-012-0353-1
132. Pacheco R, Ciruela F, Casado V, Mallol J, Gallart T, Lluis C, et al. Group i metabotropic glutamate receptors mediate a dual role of glutamate in t cell activation. J Biol Chem. (2004) 279:33352–8. doi: 10.1074/jbc.M401761200
133. Pacheco R, Oliva H, Martinez-Navio JM, Climent N, Ciruela F, Gatell JM, et al. Glutamate released by dendritic cells as a novel modulator of t cell activation. J Immunol. (2006) 177:6695–704. doi: 10.4049/jimmunol.177.10.6695
134. Magistretti PJ, Pellerin L. Cellular mechanisms of brain energy metabolism and their relevance to functional brain imaging. Philos Trans R Soc Lond Ser B Biol Sci. (1999) 354:1155–63. doi: 10.1098/rstb.1999.0471
135. Sheldon AL, Robinson MB. The role of glutamate transporters in neurodegenerative diseases and potential opportunities for intervention. Neurochem Int. (2007) 51:333–55. doi: 10.1016/j.neuint.2007.03.012
137. El-Ansary A, Al-Ayadhi L. Gabaergic/glutamatergic imbalance relative to excessive neuroinflammation in autism spectrum disorders. J Neuroinflammation. (2014) 11:189. doi: 10.1186/s12974-014-0189-0
138. Hassan TH, Abdelrahman HM, Fattah NRA, El-Masry NM, Hashim HM, El-Gerby KM, et al. Blood and brain glutamate levels in children with autistic disorder. Res Autism Spectr Disord. (2013) 7:541–8. doi: 10.1016/j.rasd.2012.12.005
139. Essa MM, Subash S, Braidy N, Al-Adawi S, Lim CK, Manivasagam T, et al. Role of nad(+), oxidative stress, and tryptophan metabolism in autism spectrum disorders. Int J Tryptophan Res. (2013) 6:15–28. doi: 10.4137/IJTR.S11355
141. Tirouvanziam R, Obukhanych TV, Laval J, Aronov PA, Libove R, Banerjee AG, et al. Distinct plasma profile of polar neutral amino acids, leucine, and glutamate in children with autism spectrum disorders. J Autism Dev Disord. (2012) 42:827–36. doi: 10.1007/s10803-011-1314-x
145. Lim CK, Essa MM, de Paula Martins R, Lovejoy DB, Bilgin AA, Waly MI, et al. Altered kynurenine pathway metabolism in autism: implication for immune-induced glutamatergic activity. Autism Res. (2016) 9:621–31. doi: 10.1002/aur.1565
147. Croonenberghs J, Verkerk R, Scharpe S, Deboutte D, Maes M. Serotonergic disturbances in autistic disorder: L-5-hydroxytryptophan administration to autistic youngsters increases the blood concentrations of serotonin in patients but not in controls. Life Sci. (2005) 76:2171–83. doi: 10.1016/j.lfs.2004.06.032
148. Gabriele S, Sacco R, Persico AM. Blood serotonin levels in autism spectrum disorder: a systematic review and meta-analysis. Eur Neuropsychopharmacol. (2014) 24:919–29. doi: 10.1016/j.euroneuro.2014.02.004
149. Golubeva AV, Joyce SA, Moloney G, Burokas A, Sherwin E, Arboleya S, et al. Microbiota-related changes in bile acid & tryptophan metabolism are associated with gastrointestinal dysfunction in a mouse model of autism. EBioMedicine. (2017) 24:166–78. doi: 10.1016/j.ebiom.2017.09.020
150. Williams M, Zhang Z, Nance E, Drewes JL, Lesniak WG, Singh S, et al. Maternal inflammation results in altered tryptophan metabolism in rabbit placenta and fetal brain. Dev Neurosci. (2017) 39:399–412. doi: 10.1159/000471509
151. Kim CJ, Kovacs-Nolan JA, Yang C, Archbold T, Fan MZ, Mine Y. L-tryptophan exhibits therapeutic function in a porcine model of dextran sodium sulfate (dss)-induced colitis. J Nutr Biochem. (2010) 21:468–75. doi: 10.1016/j.jnutbio.2009.01.019
152. Zelante T, Iannitti RG, Cunha C, De Luca A, Giovannini G, Pieraccini G, et al. Tryptophan catabolites from microbiota engage aryl hydrocarbon receptor and balance mucosal reactivity via interleukin-22. Immunity. (2013) 39:372–85. doi: 10.1016/j.immuni.2013.08.003
153. Hashimoto T, Perlot T, Rehman A, Trichereau J, Ishiguro H, Paolino M, et al. Ace2 links amino acid malnutrition to microbial ecology and intestinal inflammation. Nature. (2012) 487:477–81. doi: 10.1038/nature11228
156. De Palma G, Collins SM, Bercik P, Verdu EF. The microbiota-gut-brain axis in gastrointestinal disorders: Stressed bugs, stressed brain or both? J Physiol. (2014) 592:2989–97. doi: 10.1113/jphysiol.2014.273995
158. Huo R, Zeng B, Zeng L, Cheng K, Li B, Luo Y, et al. Microbiota modulate anxiety-like behavior and endocrine abnormalities in hypothalamic-pituitary-adrenal axis. Front Cell Infect Microbiol. (2017) 7:489. doi: 10.3389/fcimb.2017.00489
159. O'Mahony SM, Marchesi JR, Scully P, Codling C, Ceolho AM, Quigley EM, et al. Early life stress alters behavior, immunity, and microbiota in rats: implications for irritable bowel syndrome and psychiatric illnesses. Biol Psychiatry. (2009) 65:263–7. doi: 10.1016/j.biopsych.2008.06.026
164. Macfarlane GT, Allison C, Gibson SA, Cummings JH. Contribution of the microflora to proteolysis in the human large intestine. J Appl Bacteriol. (1988) 64:37–46. doi: 10.1111/j.1365-2672.1988.tb02427.x
166. Arnold GL, Hyman SL, Mooney RA, Kirby RS. Plasma amino acids profiles in children with autism: potential risk of nutritional deficiencies. J Autism Dev Disord. (2003) 33:449–54. doi: 10.1023/A:1025071014191
170. Finegold SM, Dowd SE, Gontcharova V, Liu C, Henley KE, Wolcott RD, et al. Pyrosequencing study of fecal microflora of autistic and control children. Anaerobe. (2010) 16:444–53. doi: 10.1016/j.anaerobe.2010.06.008
171. Williams BL, Hornig M, Buie T, Bauman ML, Cho Paik M, Wick I, et al. Impaired carbohydrate digestion and transport and mucosal dysbiosis in the intestines of children with autism and gastrointestinal disturbances. PLoS ONE. (2011) 6:e24585. doi: 10.1371/journal.pone.0024585
172. Williams BL, Hornig M, Parekh T, Lipkin WI. Application of novel pcr-based methods for detection, quantitation, and phylogenetic characterization of sutterella species in intestinal biopsy samples from children with autism and gastrointestinal disturbances. mBio. (2012) 3:e00261–11. doi: 10.1128/mBio.00261-11
174. Davila AM, Blachier F, Gotteland M, Andriamihaja M, Benetti PH, Sanz Y, et al. Intestinal luminal nitrogen metabolism: role of the gut microbiota and consequences for the host. Pharmacol Res. (2013) 68:95–107. doi: 10.1016/j.phrs.2012.11.005
175. Frye RE, Rose S, Slattery J, MacFabe DF. Gastrointestinal dysfunction in autism spectrum disorder: the role of the mitochondria and the enteric microbiome. Microb Ecol Health Dis. (2015) 26:27458. doi: 10.3402/mehd.v26.27458
176. Wang L, Christophersen CT, Sorich MJ, Gerber JP, Angley MT, Conlon MA. Elevated fecal short chain fatty acid and ammonia concentrations in children with autism spectrum disorder. Dig Dis Sci. (2012) 57:2096–102. doi: 10.1007/s10620-012-2167-7
177. MacFabe DF, Cain DP, Rodriguez-Capote K, Franklin AE, Hoffman JE, Boon F, et al. Neurobiological effects of intraventricular propionic acid in rats: possible role of short chain fatty acids on the pathogenesis and characteristics of autism spectrum disorders. Behav Brain Res. (2007) 176:149–69. doi: 10.1016/j.bbr.2006.07.025
178. MacFabe DF, Cain NE, Boon F, Ossenkopp KP, Cain DP. Effects of the enteric bacterial metabolic product propionic acid on object-directed behavior, social behavior, cognition, and neuroinflammation in adolescent rats: relevance to autism spectrum disorder. Behav Brain Res. (2011) 217:47–54. doi: 10.1016/j.bbr.2010.10.005
179. Ossenkopp KP, Foley KA, Gibson J, Fudge MA, Kavaliers M, Cain DP, et al. Systemic treatment with the enteric bacterial fermentation product, propionic acid, produces both conditioned taste avoidance and conditioned place avoidance in rats. Behav Brain Res. (2012) 227:134–41. doi: 10.1016/j.bbr.2011.10.045
181. Gao J, Xu K, Liu H, Liu G, Bai M, Peng C, et al. Impact of the gut microbiota on intestinal immunity mediated by tryptophan metabolism. Front Cell Infect Microbiol. (2018) 8:13. doi: 10.3389/fcimb.2018.00013
182. Anderson G, Maes M, Berk M. Inflammation-related disorders in the tryptophan catabolite pathway in depression and somatization. Adv Protein Chem Struct Biol. (2012) 88:27–48. doi: 10.1016/B978-0-12-398314-5.00002-7
183. Nikolaus S, Schulte B, Al-Massad N, Thieme F, Schulte DM, Bethge J, et al. Increased tryptophan metabolism is associated with activity of inflammatory bowel diseases. Gastroenterology. (2017) 153:1504–1516.e1502. doi: 10.1053/j.gastro.2017.08.028
184. Inoue R, Sakaue Y, Sawai C, Sawai T, Ozeki M, Romero-Perez GA, et al. A preliminary investigation on the relationship between gut microbiota and gene expressions in peripheral mononuclear cells of infants with autism spectrum disorders. Biosci Biotechnol Biochem. (2016) 80:2450–8. doi: 10.1080/09168451.2016.1222267
185. Strati F, Cavalieri D, Albanese D, De Felice C, Donati C, Hayek J, et al. New evidences on the altered gut microbiota in autism spectrum disorders. Microbiome. (2017) 5:24. doi: 10.1186/s40168-017-0242-1
186. Tomova A, Husarova V, Lakatosova S, Bakos J, Vlkova B, Babinska K, et al. Gastrointestinal microbiota in children with autism in slovakia. Physiol Behav. (2015) 138:179–87. doi: 10.1016/j.physbeh.2014.10.033
188. Shen X, Miao J, Wan Q, Wang S, Li M, Pu F, et al. Possible correlation between gut microbiota and immunity among healthy middle-aged and elderly people in southwest china. Gut Pathog. (2018) 10:4. doi: 10.1186/s13099-018-0231-3
190. Ren W, Chen S, Yin J, Duan J, Li T, Liu G, et al. Dietary arginine supplementation of mice alters the microbial population and activates intestinal innate immunity. J Nutr. (2014) 144:988–95. doi: 10.3945/jn.114.192120
191. Zhang Y, Lu T, Han L, Zhao L, Niu Y, Chen H. L-glutamine supplementation alleviates constipation during late gestation of mini sows by modifying the microbiota composition in feces. Biomed Res Int. (2017) 2017:4862861. doi: 10.1155/2017/4862861
194. Yang Z, Huang S, Zou D, Dong D, He X, Liu N, et al. Metabolic shifts and structural changes in the gut microbiota upon branched-chain amino acid supplementation in middle-aged mice. Amino Acids. (2016) 48:2731–45. doi: 10.1007/s00726-016-2308-y
195. Vojdani A, Lambert J, Vojdani E. Blood-based markers in autism spectrum disorders. Int Med Rev. (2017) 3:1–30. Available online at: https://www.researchgate.net/publication/321642638_Blood-based_markers_in_autism_spectrum_disorders_Blood-based_markers_in_autism_spectrum_disorders
Keywords: autism spectrum disorder, amino acids, mammalian target of rapamycin, nutritional intervention, gut-immune-brain axis
Citation: van Sadelhoff JHJ, Perez Pardo P, Wu J, Garssen J, van Bergenhenegouwen J, Hogenkamp A, Hartog A and Kraneveld AD (2019) The Gut-Immune-Brain Axis in Autism Spectrum Disorders; A Focus on Amino Acids. Front. Endocrinol. 10:247. doi: 10.3389/fendo.2019.00247
Received: 18 December 2018; Accepted: 29 March 2019;
Published: 16 April 2019.
Edited by:John Bienenstock, McMaster University, Canada
Reviewed by:Arturo Ortega, Centro de Investigación y de Estudios Avanzados (CINVESTAV), Mexico
Elena Gonzalez-Rey, Instituto de Parasitología y Biomedicina López-Neyra (IPBLN), Spain
Copyright © 2019 van Sadelhoff, Perez Pardo, Wu, Garssen, van Bergenhenegouwen, Hogenkamp, Hartog and Kraneveld. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Aletta D. Kraneveld, email@example.com