Impact Factor 5.511
2017 JCR, Clarivate Analytics 2018

Among the world's top 10 most-cited Immunology journals

Original Research ARTICLE

Front. Immunol., 04 January 2019 | https://doi.org/10.3389/fimmu.2018.03001

Circulating Senescent T Cells Are Linked to Systemic Inflammation and Lesion Size During Human Cutaneous Leishmaniasis

Luciana P. Covre1, Régia F. Martins1, Oliver P. Devine2, Emma S. Chambers2, Milica Vukmanovic-Stejic2, Juliana A. Silva1, Reynaldo Dietze1,3, Rodrigo R. Rodrigues1, Herbert L. de Matos Guedes4, Aloísio Falqueto5, Arne N. Akbar2* and Daniel C. O. Gomes1,6*
  • 1Núcleo de Doenças Infecciosas, Universidade Federal do Espírito Santo, Vitória, Brazil
  • 2Division of Infection and Immunity, University College London, London, United Kingdom
  • 3Saúde Global e Medicina Tropical, Instituto de Higiene e Medicina Tropical, Universidade Nova de Lisboa, Lisbon, Portugal
  • 4Instituto de Biofísica Carlos Chagas Filho, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil
  • 5Departamento de Medicina Social, Universidade Federal do Espírito Santo, Vitória, Brazil
  • 6Núcleo de Biotecnologia, Universidade Federal do Espírito Santo, Vitória, Brazil

Leishmania (Viannia) braziliensis induces American tegumentary leishmaniasis that ranges in severity from the milder form, cutaneous (CL) to severe disseminated cutaneous leishmaniasis. Patients with CL develop a cell-mediated Th1 immune response accompanied by production of inflammatory cytokines, which contribute to parasite control and pathogenesis of disease. Here, we describe the accumulation of circulating T cells with multiple features of telomere dependent-senescence including elevated expression of CD57, KLRG-1, and γH2AX that have short telomeres and low hTERT expression during cutaneous L. braziliensis infection. This expanded population of T cells was found within the CD45RA+CD27 (EMRA) subset and produced high levels of inflammatory cytokines, analogous to the senescence-associated secretory profile (SASP) that has been described in senescent non-lymphoid cells. There was a significant correlation between the accumulation of these cells and the extent of systemic inflammation, suggesting that they are involved in the inflammatory response in this disease. Furthermore, these cells expressed high level of the skin homing receptor CLA and there was a highly significant correlation between the number of these cells in the circulation and the size of the Leishmania-induced lesions in the skin. Collectively our results suggest that extensive activation during the early stages of leishmaniasis drives the senescence of T cells with the propensity to home to the skin. The senescence-related inflammatory cytokine secretion by these cells may control the infection but also contribute to the immunopathology in the disease.

Introduction

Parasites belonging to the Leishmania genus are among of the most diverse human pathogens in terms of both geographical distribution and clinical manifestations. Worldwide, 350 million people are at risk of acquiring the disease, 1.5–2 million new cases of Leishmania occur each year, and leishmaniasis causes 70,000 deaths per year in 88 tropical and subtropical countries. The disease ranges from a localized cutaneous to a fatal visceral form, depending on parasite species and host immunity (1).

Parasites from the Viannia subgenus that include Leishmania (Viannia) braziliensis are the most widespread species in the Americas, causing cutaneous leishmaniasis (CL) (1). The development of cutaneous lesions during CL is prevalent in more than 90% of cases and is characterized by an intense local cell-mediated Th1 immune response and production of inflammatory cytokines, which contribute to parasite control and tissue damage (2, 3). In addition, increased production of pro-inflammatory mediators, such as TNF-α, C-reactive protein (CRP), and adenosine deaminase (ADA) are observed in patients infected with Leishmania and may play an important role in the pathogenesis of disease (4, 5).

Immunosenescence is a term used to define the physiological decline in immune functions associated with the impaired ability of the host to mount an effective immune responses (6). In humans, immunosenescence naturally occurs with aging or is driven by chronic inflammatory conditions, inducing multiple phenotypic and dysfunctional characteristics in the T-cell pool (7).

Senescent T cells have been described in human CD4+ and CD8+ populations (810). These cells exhibit low proliferative potential after activation, short telomeres and low telomerase activity, elevated reactive oxygen species (ROS) production, constitutive p38 MAP kinase activation, expression of DNA damage response machinery and increased cyclin-dependent kinase inhibitor p16INK4a expression (11). The senescent T cells express the CD45RA+CD27 EMRA phenotype and have preferential homing capacity for peripheral tissues (12). Furthermore, these senescent T cells, secrete high levels of pro-inflammatory cytokines that has been suggested to be a manifestation of the senescence associated secretory phenotype (SASP), as described previously in non-lymphoid cells (10, 13).

Although T cell dysfunctions are linked to increased replication and survival in parasite diseases (14, 15) there is no data associating T cell senescence and Leishmania infection so far. Here, we demonstrate that the intense inflammatory cytokine secretion that has previously been shown to occur in this disease is linked to the accumulation of senescent T cells with a SASP-like functional profile. Furthermore, these circulating cells have skin homing potential and correlate numerically with leishmanial-related skin lesion size.

Collectively our data offer a re-interpretation of the immune events that occur during leishmaniasis by demonstrating that the intensive proliferative drive to T cells induces T senescence and associated pro-inflammatory cytokine secretion that contributes to parasite control and also immunopathology during cutaneous leishmaniasis.

Materials and Methods

Study Subjects

Peripheral blood from 17 untreated cutaneous leishmaniasis (CL) patients attendant at Hospital Universitário Cassiano Antônio de Morais, Universidade Federal do Espirito Santo–Brazil were used in this study. The diagnosis of CL was determined by clinical and laboratory criteria. All patients in this study tested positive for the PCR/restriction fragment length polymorphism for L. braziliensis and reported no prior Leishmania infections or treatment (Supplementary Figure 1). The control group consisted of 15 healthy age matched individuals (HC) from non-endemic areas, without treatment history. All study participants consented to take part and were serologically negative for HIV, HBV, and HCV infection. They also had no history of chemotherapy, radiotherapy or treatment with immunosuppressive medications within the last 6 months. All volunteers and patients provided written informed consent, and study procedures were performed in accordance with the principles of the Declaration of Helsinki. The study was registered at HUCAM ethical committee under referential number 735.274.

PBMC and T Cells Isolation

PBMCs from CL and HC were isolated by centrifugation of heparinized whole blood through a Ficoll-Hypaque gradient (GE Healthcare, Uppsala, Sweden). Cryopreserved cells from both controls and patients were thawed in RPMI complete medium supplemented with 10% of fetal calf serum. Viability and recovery were measured using trypan blue dye exclusion in haemocytometer. The CD4+ and CD8+ T cell isolations were performed by negative selection using MACS cell separation (Milteny Biotec) according to the manufacturer's protocol.

Flow Cytometric Analysis

Flow cytometric analysis was carried out using the following reagents: Live/dead UV Zombie, KLRG1 APC (2F1), CD4 Brilliant Violet 711 (OKT-4), CD28 Brilliant Violet 510 (CD28.2) and CD45RA PECy7 (HI100) all from Biolegend. CD28 Brilliant Violet 786 (U28), CD3 PECF594 (UCHT1), CD8 APC-H7 (SK1), CD57 Alexa Fluor 421 (NK-1), and human cutaneous lymphocyte antigen (CLA) FITC (HECA-452) from BD Biosciences. Cell suspensions were incubated with antibody solutions for 30 min at 4°C for extracellular staining. Intracellular staining for Ki67 (clone B56, BD Bioscience) was performed with Foxp3 Staining Buffer Set (Miltenyi Biotec, Bisley, UK). Cytokine and anti-hTERT (rabbit IgG—Abcam) staining were performed using Fix and Perm Cell Permeabilization Kit (Invitrogen, Paisley, UK) according to the manufacturer's protocol. Samples were processed at Fortessa X-20 cytometer (BD Biosciences) and analyzed using FlowJo software (Treestar). Isotype control staining and fluorescence-minus-one controls were used to set the quadrants.

Phospho-Flowcytometry

The levels of p38 (pT180/pY182) Alexa Fluor 488 and γH2AX (pSer139) Alexa Fluor 647 (B56), all from BD Biosciences were analyzed ex vivo in PBMCs fixed with warm Cytofix Buffer (BD Biosciences) at 37°C for 10 min. Cells were permeabilized with ice-cold Perm Buffer III (BD Biosciences) at 4°C for 30 min and incubated with the respective antibodies for 30 min at room temperature.

Cytokine Determination

Cytokine production was determined in the supernatant of PBMC unstimulated or stimulated samples with 10 μg/ml of L. braziliensis promastigote antigens (LbAg) or 0.5 μg/mL plate-coated anti-CD3 (OKT3) (Biolegend) in the presence of 5 ng/mL of rhIL-2 for 72 h. IFN-γ, TNF-α, Granzyme B, IL-10, and IL-4 levels were assayed by Cytokine Bead Array (CBA) (BD Biosciences) according to the manufacturer's protocol. Serum evaluation of IL-10, IFN-γ, TNF-α, and CRP levels were performed by ELISA assay according to the manufacturer's protocol (R&D systems).

Proliferation Assay

Proliferation was performed by using PBMC unstimulated or stimulated with 0.5 μg/mL plate-coated anti-CD3 (OKT3) (Biolegend) in the presence of 5 ng/mL of rhIL-2 for 72 h followed of evaluation by intracellular staining for the cell cycle related nuclear antigen Ki67 by flow cytometry.

Telomere Fluorescence in situ Hybridisation

CD4+ and CD8+ T cells were isolated (as above) from HC and CL samples and prepared on poly-L-lysine coated glass slides by cytocentrifugation (Cytospin, Thermo Scientific, USA). Cytological specimens were then dried and fixed in ethanol/acetone prior to freezing. Specimens were thawed prior to staining. Specimens were PFA fixed, dehydrated in cold ethanol prior to permeabilization and blocking with BSA. Slides were washed prior to further dehydration across an ethanol gradient and air dried prior to hybridization with the PNA probe (Panagene, TelC Cy3, #14 1224PL-01) for 2 h in the dark as described in (16). Slides were subsequently washed in formamide/SSC prior to mounting with Vectorshield/DAPI (Vector Laboratories, USA). Imaging was performed using a Leica SPE2 confocal microscope using LAS X version 3.3.0 software (Leica Microsystem, Wetzlar, Germany). The images corresponded to a full z stack of CD4 or CD8 T cells were analyzed using ImageJ software.

t-SNE Analysis

Unbiased representations of multi-parameter flow cytometry data were generated using the t-distributed stochastic neighbor embedding (t-SNE) algorithm. The R package “Rtsne” available on CRAN (github.com/jkrijthe/Rtsne) was used to perform the Barnes Hut implementation of t-SNE on flow cytometry data. FlowJo software was used to export events of interest (in fcs format) for each sample. After using the Bioconductor “flowCore” R package to import.fcs file data and the Logicle transform to scale the data similarly to that displayed in FlowJo, 10.000 events from each samples analyzed in parallel were merged and the relevant fluorescent parameters were used. t-SNE is a non-linear dimensionality reduction method that optimally places cells with similar expression levels near to each other and cells with dissimilar expression levels further apart.

Statistics

GraphPad Prism was used to perform statistical analysis. KS normality test was prior performed and the statistical significance was evaluated using Student t-test for paired samples or repeated-measures ANOVA with Tukey correction used for post-hoc testing. A Mann-Whitney test was performed for all continuous, non-parametric variables. Differences were considered significant when P was < 0.05.

Results

T Cells From Cutaneous Leishmaniasis Patients Exhibit Characteristics of Senescence

Senescent T cells demonstrate both intra- and extra- cellular phenotypic changes as well as functional defects often implicated in the susceptibility of host immunity. We observed increased frequencies of the cells surface senescence associated markers CD57 in CD4+ and CD8+ T cells (Figure 1A) and the inhibitory killer cell lectin-like receptor G1 (KLRG1) in CD8+ T cells in CL patients compared to controls (Figure 1B). T cells from patients also expressed more of the DNA damage-related protein γH2AX (Figure 1C) and exhibited elevated phosphorylation of p38 protein that was significantly higher in CD4+ and CD8+ T cells than controls (Figure 1D). In addition, confocal microscopy analysis demonstrated shorter telomeres in both CD4+ and CD8+T cells that were significantly shorter than observed in the HC control group (Figure 1E). Therefore, T cells that exhibit multiple characteristics of senescence accumulate in patients with CL.

FIGURE 1
www.frontiersin.org

Figure 1. Characterization of senescent markers in T cells during cutaneous leishmaniasis. CD4+ and CD8+ T cells isolated from healthy controls (HC) (n = 14) and patients with active cutaneous leishmaniasis patients (CL) (n = 16) were stained for CD57, KLRG1, phosphorylated histone H2AX (γH2AX) or phosphorylated p38 protein and analyzed by flow cytometry. Representative cytometry plots and cumulative data of CD57 (A), KLRG1 (B), γH2AX- expressing cells (C), fold change of fluorescence intensity of phospho-p38 protein (D), telomere FISH image in purified CD4+ and CD8+ T cells hybridized with telomere probe and fold change of quantitative fluorescence intensity levels normalized with HC group (E). The graphs show the mean ± SEM. P-values were calculated using repeated-measures ANOVA with the Tukey correction used for post-hoc testing. *p < 0.05, **p < 0.01, ****p < 0.0001.

Senescent T Cells From Cutaneous Leishmaniasis Patients Are Found Within the EMRA Population

Both CD8+ and CD4+ T cells can be subdivided into four populations on the basis of their relative surface expression of CD27 and CD45RA molecules. This can define naive (CD45RA+CD27+), central memory (CM; CD45RACD27+), effector memory (EM; CD45RACD27), and effector memory T cells that re-express CD45RA (EMRA; CD45RA+CD27) that contain the majority of senescent T cells (8). CL patients possess increased frequencies of effector memory (EM) and EMRA and decreased central memory (CM) populations in both CD4+ and CD8+ T cell subsets (Figures 2A,B). No difference in total circulating white cell count was observed between healthy controls and CL patients (Supplementary Figure 1) indicating a proportional increase of these cells in the circulating CD4+ and CD8+ subsets.

FIGURE 2
www.frontiersin.org

Figure 2. End-stage memory T cells (EMRA) accumulate during the CL and displays functional characteristics of senescence. Representative plots and cumulative data of percentage of CD4+ (A) and CD8+ (B) T cells subsets isolated from HC (n = 12) or CL (n = 14) and characterized by expressing CD45RA and CD27 markers (naive-CD45RA+ CD27+; CM-central memory, CD45RA CD27+; EM-effector memory, CD45RACD27; and EMRA-effector memory T cells that re-express CD45RA, CD45RA+ CD27). Frequencies of CD27 and CD28 co-stimulatory molecules loss within CD4+ and CD8+ EMRA subset (C). Proliferative capacity evaluated by Ki67 staining (D) and telomerase reverse transcriptase (hTERT) MFI (E) of CD4+ and CD8+ EMRA subset (F) from HC or CL stimulated with 0.5μg/mL of anti-CD3 for 72 h. The graphs show the mean ± SEM. P-values were calculated using repeated measures ANOVA with the Tukey correction used for post-hoc testing. *p < 0.05, ** p < 0.01, ***p < 0.001, ****p < 0.0001.

Chronic infection and continuous antigen-specific stimulation of T cells induces loss of co-stimulatory receptors, such as CD28 and CD27 and replicative capacity resulting from telomere shortening and decreased activity of the enzyme telomerase. The CL-EMRA T cell subset within both CD4+ and CD8+ compartments have lost CD27 and CD28 coexpression (Figure 2C) and demonstrated diminished proliferative capacity (Figure 2D) that was also observed in both CM and EF memory subsets (Supplementary Figure 2) and identified by Ki67 staining, after polyclonal stimulation in vitro. We analyzed the expression of catalytic telomerase component (hTERT) within CD4+ and CD8+ EMRA from both groups and found that CL patients exhibit decreased expression of hTERT compared to controls (Figures 2E,F). This observation was extended to CM and EM memory subsets of both compartments (CD4+ and CD8+) in response to activation (data no shown). Therefore, the EMRA subset that accumulates during CL exhibits phenotypic as well as functional characteristics of senescence.

T Cells From Cutaneous Leishmaniasis Patients Exhibit a Pro-Inflammatory Functional Phenotype

The abundant capacity to secrete pro-inflammatory mediators including cytokines has been associated with aging and chronic infections. Compared to controls, the PBMC from CL patients secreted significantly higher levels of IFN-γ, TNF-α, and Granzyme B after anti-CD3 stimulation (Figure 3). In addition, L. braziliensis antigen (LbAg) stimulation induced high levels of these mediators in CL patients but not in the healthy controls, suggesting that there is an accumulation of parasite specific T cells with a secretory profile in these individuals. While IL-10 was induced after anti-CD3 stimulation of patients and controls, LbAg stimulation did not induce this inhibitory cytokine in CL patients indicating an imbalance of pro-inflammatory vs. anti-inflammatory cytokines in response to specific antigen stimulation.

FIGURE 3
www.frontiersin.org

Figure 3. Cytokines production by activated cells. PBMC from HC (n = 13) or CL (n = 14) groups were cultured with 10 μg/ml of L. braziliensis promastigote antigens (LbAg) or 0.5 μg/mL of anti-CD3 for 72 h. Production of IFN-γ, TNF-α, Granzyme B, and IL-10 were determined in the culture supernatants by CBA. The graphs show the mean ± SEM. P-values were calculated using repeated measures ANOVA with the Tukey correction used for post-hoc testing. **p < 0.01, ***p < 0.001, ****p < 0.0001.

To investigate the pro-inflammatory cytokine secretion in more detail we used the t-Distribution Stochastic Neighbor Embedding (t-SNE) algorithm, which projects high dimensional data into two dimensional space (t-SNE1 and t-SNE2) through performing repeated pairwise comparison of randomly selected cellular phenotypes based on their marker expression—ultimately clustering closely related cells. This allowed us to characterize the phenotypic diversity identified by specific clusters associated with granular contents (Granzyme B, Perforin, and CD107a) and cytokines (IFN-γ, TNF-α) on CD4+ (Figures 4A,B) and CD8+ T cells (Figures 4D,E) obtained from healthy controls and CL patients. The relative low expression of pro- inflammatory mediators in HC were combined with a strong expression of them in both T cell compartments of CL patients. This indicates the differential composition of functional markers with the predominance of TNF-α, CD107a, and perforin associated to CL-CD4+ (2, 4, 14, and 19) and CD8+ (7, 8, 10, 16, 13, and 15) clusters, but not in controls, as presented in the heat map (Figures 4C,F).

FIGURE 4
www.frontiersin.org

Figure 4. Pro-inflammatory cytokines and cytotoxic granules are highly diverse across CD4+ and CD8+ T cells from HC and CL patients. PBMC from healthy donors (HC) (n = 14) and cutaneous leishmaniasis patients (CL) (n = 16) were stimulated with 0.5 μg/mL of anti-CD3 for 24 h and stained for surface and intra-cellular markers for cytometry analysis. t-SNE was performed gating on CD4+ and CD8+ T cells, which are identified general differences in functional markers expression between both compartments from HC and CL groups and evidenced by the numbered and colored clusters (A,D). The expression of granzyme B, IFN-γ, TNF-α, CD27, CD45RA, perforin, and CD107a were evaluated separately on live CD4+ and CD8+ T cells (B,E). Heatmap showing hierarchical clusters and functional markers expression levels of CD4+ and CD8+ T cells from HC and CL patients (C,F). Normalized protein expression levels were represented in red for high expression, whereas blue represents low expression (cold-to-hot heat map).

To investigate this further we examined the secretory phenotype of cytokine-producing T cells within CL patient and HC by flow cytometric analysis using the expression of senescence surface markers CD45RA and CD27. Ex vivo and polyclonal stimulation analyses demonstrated increased frequencies of senescent T cells subset (EMRA) within both CD8+ (Figure 5) and CD4+ T cells (data not shown) from CL patients that produce IFN-γ, TNF-α, Granzyme B, Perforin, and CD107a, supporting the pro-inflammatory secretory profile of these populations.

FIGURE 5
www.frontiersin.org

Figure 5. EMRA subsets from CL patients present evident senescent-associated secretory phenotype. Cumulative data of perforin, CD107a, TNF-α, IFN-γ, and Granzyme B-producing CD8+-EMRA frequencies from HC (n = 11) and CL (n = 13) unstimulated or stimulated with 0.5 μg/mL of anti-CD3 stimulation for 24 h. The graphs show the mean ± SEM. P-values were calculated using repeated measures ANOVA with the Tukey correction used for post-hoc testing. **p < 0.01, ***p < 0.001, ****p < 0.0001.

CL Patients Have Increased Systemic Inflammation That Correlates With the Accumulation of Senescent (EMRA) and Effector Memory T Cells

Systemic production of pro-inflammatory mediators is linked to the development of phenotypic and dysfunctional senescence features of T cells. Thus, we performed a serological analysis for some common immune mediators in both HC and CL groups. CL patients had increased systemic levels of C-reactive protein (CRP), IFN-γ, and TNF-α (Figure 6A), which correlated significantly with the accumulation of senescent CD8+ (Figure 6B) and CD4+ (Supplementary Figure 3) T cell subsets. Moreover, CRP levels correlated positively with the accumulation of EF memory T cell within both CD4+ and CD8+, but not naïve or central memory subsets (Supplementary Figure 4). There was no correlation between the level of IL-10 and EMRA T cells further suggesting an imbalance between pro and anti-inflammatory cytokines in CL patients. There was also no correlation between the levels of these cytokines and the CM or EM memory T cell subsets (data not shown).

FIGURE 6
www.frontiersin.org

Figure 6. Inflammatory profile is exhibited in the serum of CL patients and correlates with EMRA frequency. Serological analysis of C-reative protein (CRP), IFN-γ, TNF-α, and IL-10 levels in CL patients (n = 16) and healthy control group (HC) (n = 15) (A). Correlation between cytokines or CRP levels and frequency of CD8+ EMRA T cells in HC (○) or CL patients (■) were tested using Pearson's correlation test (B). For all tests, a *p < 0.05, ****p < 0.0001 were considered statistically significant.

Circulating Senescent (EMRA) T Cells Correlate With Lesion Size and Propensity for Skin Homing After L. braziliensis Antigen Stimulation

As senescent T cells that accumulated in CL patients were pro-inflammatory, especially after stimulation with L. braziliensis antigens, we investigated if they were associated with the skin immunopathology that occurs during the infection. To do this we correlated the EMRA CD4+ and CD8+ T cell subsets with the size of the skin lesions in patients with cutaneous leishmaniasis (Figure 7A). We found a strong correlation between the EMRA CD4+ and moderate correlation between CD8+ T cell subsets cells with lesion size suggesting that these circulating cells contributed to skin immunosurveillance and immunopathology during the course of the disease. The same correlation was observed with EM subset from both compartments, supporting previous observations (1719).

FIGURE 7
www.frontiersin.org

Figure 7. CL- EMRA subset correlates with lesion size and up regulate the skin homing receptor cutaneous leucocyte-associated antigen (CLA). Pearson's correlation test between frequencies of CD4+ and CD8+ T subsets (Naïve, CM, EF, and EMRA) and lesions size (mm2) of CL patients (n = 14) (A,B). Cumulative data of CLA- expressing T cell subsets from HC and CL (C) in response to 10 μg/ml of L. braziliensis promastigote antigen (LbAg) stimulation for 72 h and analyzed by flow cytometry. The graphs show the mean ± SEM. P-values were calculated using repeated measures ANOVA with the Tukey correction used for post-hoc testing. *p < 0.05, **p < 0.01, ***p < 0.001, ****p < 0.0001.

We therefore evaluated the ability of EMRA subsets to regulate the skin homing receptors cutaneous leucocyte-associated antigen (CLA) and chemokine receptor CCR4 before and after activation with LbAg. Polyclonal activation with anti-CD3 induced increased expression of CLA in both CL and HC groups (not shown), however EMRAs and EM from CL upregulated the CLA expression in response to L. braziliensis antigen recall (Figures 7B,C). Circulating CD4+ and CD8+ T cells showed higher frequencies of CLA compared to HC group (Supplementary Figure 5) confirming previous reports (18, 19). However, we extended previous observations by showing that LbAg induced high levels of CLA predominantly in EF and EMRA memory T cell subsets within both CD4+ and CD8+ compartments. These findings suggest that there is preferential induction of CLA on T cells from CL conferring increased ability to target skin lesion sites. No differences in CCR4 expression were observed between HC and CL groups in none of the conditions evaluated (data not shown).

Discussion

Persistent antigenic stimulation can result in phenotypic characteristics and functional changes associated with senescence in human T cells. These include decreased responsiveness to TCR stimulation, diminished proliferative capacity, increased susceptibility to apoptosis and expression of immune inhibitory receptors (11, 20) that directly impede the host effort to mount an effective immunity against pathogens (21, 22).

In our experiments, both CD4+ and CD8+ T cells from CL patients exhibit increased expression of many senescence-related markers including CD57, KLRG1, p38 MAPK, and phosphorylation of histone protein H2AX. Although the increased expression of these markers has been described previously in aging and infection (23, 24) it was not clear if these cells also accumulated during parasitic infections. As previously reported and supported by our findings, circulating CD4+ and CD8+ T cells from CL patients demonstrated higher expression of CD57 as compared to healthy controls (25, 26), and this was also observed in T cells from the lesions of CL patients or during visceral leishmaniasis (27).

KLRG1 expression has been shown to impair microbicidal function of NK cells and CD8+ T cells (28, 29) and this may have an impact on host immunity during Leishmania infections. In addition, murine CD8+ T cells expressing KLRG1 downregulate its receptor under pro-inflammatory conditions, which is essential for developing peripheral and tissue-resident memory cells with increased proliferative capacity (30); this supports the limitation of the isolated use of KLRG1 as a senescent marker. However, in the present and previous studies (31), we have used KLRG1 expression in conjunction with other markers to define senescent T cells.

The phosphorylation of both p38MAPK and H2AX is induced in response to telomere shortening, which have been associated with proliferative defect in human T cells (32). This is related to minimal telomerase activity that in other situations can be restored with the transduction of hTERT resulting in telomere elongation and an increase in replicative life span after stimulation (8, 33). Consistent with these, both CD4+ and CD8+ T cells from CL patients show short telomeres and low expression of the catalytic telomerase component in memory subsets.

Similar to our findings, continued antigenic exposure drives the expansion and differentiation of both CD4+ and CD8+ T cells to an end-stage/senescent population that re-express CD45RA associated with the loss of CD27/CD28 co-stimulatory receptors (EMRA). As extensively demonstrated in HIV and CMV infections these populations exhibit decreased proliferative capacity, as demonstrated here and increased propensity to apoptosis and decreased TCR stimulation (20). Although we did not perform analyzes regarding propensity to apoptosis and decreased TCR stimulation that could be a limitation to the study, our previous observations we have demonstrated that T cells with the phenotype of senescent cells as described here do exhibit these characteristics (9, 34).

Cutaneous leishmaniasis caused by L. braziliensis is also are associated with potent Th1-type responses and chronic production of pro-inflammatory cytokines (2, 3). Although these responses are beneficial for the activation of leishmanicidal mechanisms and parasite control, the exaggerated inflammation contributes to the development of skin lesions and tissue destruction observed in human ML and CL patients (35, 36). He we show that the inflammatory T cells that accumulate in the circulation of infected individuals have characteristics of senescent cells and since they are highly secretory, they may have the equivalent of a senescence-associated secretory phenotype (SASP) (13). In addition, we consider that the extent of senescence may depend on the clinical type of leishmaniasis as well as during other parasitic infections (27, 37, 38). A key observation was that the stimulation with Leishmania antigens induced an imbalance in the pro vs. anti-inflammatory cytokine ratio compared with anti-CD3 activation of T cells from infected patients. In patients and murine models, the exacerbated production of IFN-γ and TNF-α, and the decreased production of IL-10 positively correlate with lesions size in CL and tissue damage in severe mucosal leishmaniasis (ML) (35, 36). Intralesional analysis of cytokine gene expression has shown high frequencies of granzyme, IL-2, IFN-γ, and TNF-α and enrichment of Leishmania-specific CD8+ T (19, 39). Moreover, patients treated with anti-inflammatory drugs show increased healing of lesions, supporting the deleterious role of inflammation (40, 41). High frequencies of cytotoxic cells were observed in lesions of patients with CL caused by L. braziliensis and correlated with inflammatory potential and cutaneous tissue damage. Moreover, the exaggerated inflammation correlates with increased tissue hyperplasia, granuloma development, T cells apoptosis and susceptibility to visceral leishmaniasis (19, 39, 42).

Increased inflammatory markers have been linked to a wide variety of adverse outcomes and chronic conditions, even as reciprocally impaired antigen-specific immune responses compromise protective capacities (43). According to our experiments, increased levels of pro-inflammatory mediators are observed systemically in patients with both CL and ML or induced in vitro after specific-antigen recall (5, 44, 45). Inflammatory products, such as TNF-α, IL-1β, CRP are potent inductor of phenotypic and dysfunctional senescence features of T cells accelerating the impairment of the immune effector function (7).

We now show that circulating senescent cells in infected individuals have increased potential to home to the skin as indicated by high CLA expression, extending previous reports that demonstrate the up regulation of this receptor in circulating and local effector memory T cells (1719). CLA is a unique skin-homing receptor expressed by circulating memory T cells that infiltrate the skin which facilitates targeting of T cells to inflamed skin, which also has been associated with the pathogenesis or severity of many inflammatory skin diseases, such as leprosy, atopic dermatitis and psoriasis (46, 47). Furthermore, the activation of T cells from patients with L. braziliensis antigens in vitro further induced the expression of CLA but not CCR4 on the senescent T cells. During Leishmania infection skin homing receptors can be induced by proinflammatory mediators, such as IL-1 and TNF-α as consequence of tissue injury and systemic inflammation (40). CLA-positive cells can use both VLA-4/VCAM-1 and LFA-1/ICAM-1 for extravasation on skin surfaces (48), which could account the enrichment of T cells expressing this receptor in the lesion of cutaneous leishmaniasis patients (18, 49).

The observation of a positive correlation between the accumulation of circulating senescent T cells and lesion size provides a link between events in the blood and in the skin suggesting that the recruitment of these proinflammatory cells, resulting from increased CLA expression, may contribute to the skin pathology in CL.

The findings presented here demonstrate that senescent T cells with a unique functional profile are extensively induced by telomere dependent-senescence during cutaneous leishmaniasis. This study identifies the role of cellular senescence in regulating the function of parasite-specific T cells and demonstrates that these cells can also be associated with the immunopathology that occurs during acute infection.

Author Contributions

LC, RM, OD, HdM, JS, and DG performed experiments. LC, DG, OD, and EC analyzed data. AF selected the patients. DG, AA, RD, and MV-S designed the project and discussed data. DG, AA, MV-S, RR, and EC wrote the manuscript the support of all other co-authors.

Funding

This work was supported by Fundação de Amparo a Pesquisa do Espírito Santo-FAPES/Newton Fund and Medical Research Council-UK (Grant 72939273/16) and Coordination for the Improvement of Higher Education Personnel—CAPES-Brazil - Code 001.

Conflict of Interest Statement

The 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.

Acknowledgments

The authors would like to thank Dr. Bruna Mendonça Portela (HUCAM-UFES) and Dr. Lorenzzo Lyrio Stringari for CRP and serological cytokine evaluations and Dr. Alessio Lanna (Kennedy Institute of Rheumatology—UK) for the scientific discussion.

Supplementary Material

The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fimmu.2018.03001/full#supplementary-material

Supplementary Figure 1. Clinical features of cutaneous leishmaniasis patients and healthy controls participating in the study. NA, Not applicable.

Supplementary Figure 2. Proliferative capacity evaluated by Ki67 staining of CD4+ and CD8+ subsets [Naïve; Central memory (CM) and Effector memory (EF)] from HC or CL stimulated with 0.5 μg/mL of anti-CD3 for 72 h. The graphs show the mean ± SEM. P-values were calculated using repeated measures ANOVA with the Tukey correction used for post-hoc testing. **p < 0.01, ****p < 0.0001.

Supplementary Figure 3. Correlation between cytokines levels and frequency of CD4+ EMRA subset in HC (○) or CL patients (■) were tested using Pearson's correlation test. For all tests, a p < 0.05 was considered statistically significant.

Supplementary Figure 4. Inflammatory profile correlates with differentiation state. Correlation between cytokines levels and frequency of CD4 (A) and CD8 (B) subsets in HC or CL patients were tested using Pearson's 1124 correlation test. For all tests, a p < 0.05 was considered statistically significant.

Supplementary Figure 5. Characterization of CLA expression in T cells during cutaneous leishmaniasis. CD4+ and CD8+ T cells isolated from healthy controls (HC) (n = 12) and patients with active cutaneous leishmaniasis patients (CL) (n = 14) were stained for cutaneous leucocyte-associated antigen (CLA) and analyzed by flow cytometry. Representative cytometry plots and cumulative data of CLA- expressing cells. The graphs show the mean ± SEM. P-values were calculated using repeated-measures ANOVA with the Tukey correction used for post-hoc testing. ****p < 0.0001.

References

1. WHO. Leishmaniasis. WHO (2016). Available online at: http://whqlibdoc.who.int/trs/WHO_TRS_949_eng.pdf

2. Scott P, Novais FO. Cutaneous leishmaniasis: immune responses in protection and pathogenesis. Nat Rev Immunol. (2016) 16:581–92. doi: 10.1038/nri.2016.72

PubMed Abstract | CrossRef Full Text | Google Scholar

3. Pirmez C, Yamamura M, Uyemura K, Paes-Oliveira M, Conceicao-Silva F, Modlin RL. Cytokine patterns in the pathogenesis of human Leishmaniasis. J Clin Invest. (1993) 91:1390–5. doi: 10.1172/JCI116341

PubMed Abstract | CrossRef Full Text | Google Scholar

4. Junior ADO, Machado P, Bacellar O, Cheng LH. Evaluation of IFN-γ and TNF-α as immunological markers of clinical outcome in cutaneous leishmaniasis IFN-γ e TNF-α como marcadores da resposta clínica na leishmaniose cutânea. Rev Soc Bras Med Trop. (2002) 35:7–10. doi: 10.1590/s0037-86822002000100002

CrossRef Full Text | Google Scholar

5. Kip AE, Balasegaram M, Beijnen JH, Schellens JHM, De Vries PJ, Dorloa TPC. Systematic review of biomarkers to monitor therapeutic response in leishmaniasis. Antimicrob Agents Chemother. (2015) 59:1–14. doi: 10.1128/AAC.04298-14

PubMed Abstract | CrossRef Full Text | Google Scholar

6. Akbar AN, Fletcher JM. Memory T cell homeostasis and senescence during aging. Curr Opin Immunol. (2005) 17:480–5. doi: 10.1016/j.coi.2005.07.019

PubMed Abstract | CrossRef Full Text | Google Scholar

7. Macaulay R, Akbar AN, Henson SM. The role of the T cell in age-related inflammation. Age (2013) 6:563–72. doi: 10.1007/s11357-012-9381-2

CrossRef Full Text | Google Scholar

8. Di Mitri D, Azevedo RI, Henson SM, Libri V, Riddell NE, Macaulay R, et al. Reversible senescence in human CD4+CD45RA+CD27 memory T cells. J Immunol. (2011) 187:2093–100. doi: 10.4049/jimmunol.1100978

PubMed Abstract | CrossRef Full Text | Google Scholar

9. Lanna A, Henson SM, Escors D, Akbar AN. The kinase p38 activated by the metabolic regulator AMPK and scaffold TAB1 drives the senescence of human T cells. Nat Immunol. (2014) 15:965–72. doi: 10.1038/ni.2981

PubMed Abstract | CrossRef Full Text | Google Scholar

10. Callender LA, Carroll EC, Beal RWJ, Chambers ES, Nourshargh S, Akbar AN, et al. Human CD8+EMRA T cells display a senescence-associated secretory phenotype regulated by p38 MAPK. Aging Cell (2018) 17:1–9. doi: 10.1111/acel.12675

PubMed Abstract | CrossRef Full Text | Google Scholar

11. Akbar AN, Henson SM, Lanna A. Senescence of T lymphocytes: implications for enhancing human immunity. Trends Immunol. (2016) 37:866–76. doi: 10.1016/j.it.2016.09.002

PubMed Abstract | CrossRef Full Text | Google Scholar

12. Henson SM, Riddell NE, Akbar AN. Properties of end-stage human T cells defined by CD45RA. Curr Opin Immunol. (2012) 24:476–81. doi: 10.1016/j.coi.2012.04.001

PubMed Abstract | CrossRef Full Text | Google Scholar

13. Tchkonia T, Zhu Y, van Deursen J, Campisi J, Kirkland JL. Cellular senescence and the senescent secretory phenotype: therapeutic opportunities. J Clin Invest. (2013) 123:966–72. doi: 10.1172/JCI64098

PubMed Abstract | CrossRef Full Text | Google Scholar

14. Gigley JP, Bhadra R, Moretto MM, Khan IA. T cell exhaustion in protozoan disease. Trends Parasitol. (2012) 28:377–84. doi: 10.1016/j.pt.2012.07.001

PubMed Abstract | CrossRef Full Text | Google Scholar

15. Rodrigues V, Cordeiro-da-Silva A, Laforge M, Ouaissi A, Akharid K, Silvestre R, et al. Impairment of T cell function in parasitic infections. PLoS Negl Trop Dis. (2014) 8:e2567. doi: 10.1371/journal.pntd.0002567

PubMed Abstract | CrossRef Full Text | Google Scholar

16. Riddell NE, Griffiths SJ, Rivino L, King DCB, Teo GH, Henson SM, et al. Multifunctional cytomegalovirus (CMV)-specific CD8+T cells are not restricted by telomere-related senescence in young or old adults. Immunology (2015) 144:549–60. doi: 10.1111/imm.12409

CrossRef Full Text | Google Scholar

17. Santamaria-Babí LF. CLA+ T cells in cutaneous diseases. Eur J Dermatol. (2004) 14:13–8.

PubMed Abstract | Google Scholar

18. Mendes-Aguiar CDO, Gomes-Silva A, Nunes E, Pereira-Carvalho R, Nogueira RS, Oliveira-Neto MDP, et al. The skin homing receptor cutaneous leucocyte-associated antigen (CLA) is up-regulated by Leishmania antigens in T lymphocytes during active cutaneous leishmaniasis. Clin Exp Immunol. (2009) 157:377–84. doi: 10.1111/j.1365-2249.2009.03970.x

CrossRef Full Text | Google Scholar

19. Santos CDS, Boaventura V, Ribeiro Cardoso C, Tavares N, Lordelo MJ, Noronha A, et al. CD8+granzyme B+-mediated tissue injury vs. CD4+IFNγ+-mediated parasite killing in human cutaneous leishmaniasis. J Invest Dermatol. (2013) 133:1533–40. doi: 10.1038/jid.2013.4

CrossRef Full Text | Google Scholar

20. Akbar AN, Beverley PCL, Salmon M. Will telomere erosion lead to a loss of T-cell memory? Nat Rev Immunol. (2004) 4:737–43. doi: 10.1038/nri1440

PubMed Abstract | CrossRef Full Text | Google Scholar

21. Nikolich-Žugich J. Ageing and life-long maintenance of T-cell subsets in the face of latent persistent infections. Nat Rev Immunol. (2008) 8:512–22. doi: 10.1038/nri2318

PubMed Abstract | CrossRef Full Text | Google Scholar

22. Goronzy JJ, Weyand CM. Understanding immunosenescence to improve responses to vaccines. Nat Immunol. (2013) 14:428–36. doi: 10.1038/ni.2588

PubMed Abstract | CrossRef Full Text | Google Scholar

23. Griffiths SJ, Riddell NE, Masters J, Libri V, Henson SM, Wertheimer A, et al. Age-associated increase of low-avidity cytomegalovirus-specific CD8+ T cells that re-express CD45RA. J Immunol. (2013) 190:5363–72. doi: 10.4049/jimmunol.1203267

PubMed Abstract | CrossRef Full Text | Google Scholar

24. Henson SM, Akbar AN. KLRG1—more than a marker for T cell senescence. Age (2009) 31:285–91. doi: 10.1007/s11357-009-9100-9

PubMed Abstract | CrossRef Full Text | Google Scholar

25. Parodi C, García Bustos MF, Barrio A, Ramos F, González Prieto AG, Mora MC, et al. American tegumentary leishmaniasis: T-cell differentiation profile of cutaneous and mucosal forms—co-infection with Trypanosoma cruzi. Med Microbiol Immunol. (2016) 205:353–69. doi: 10.1007/s00430-016-0455-0

PubMed Abstract | CrossRef Full Text | Google Scholar

26. Gomes AHS, Martines RB, Kanamura CT, Barbo MLP, Iglezias SD, Lauletta Lindoso JA, et al. American cutaneous leishmaniasis: in situ immune response of patients with recent and late lesions. Parasite Immunol. (2017) 39:e12423. doi: 10.1111/pim.12423

PubMed Abstract | CrossRef Full Text | Google Scholar

27. Casado JL, Abad-Fernández M, Moreno S, Pérez-Elías MJ, Moreno A, Bernardino JI, et al. Visceral leishmaniasis as an independent cause of high immune activation, T-cell senescence, and lack of immune recovery in virologically suppressed HIV-1-coinfected patients. HIV Med. (2015) 16:240–8. doi: 10.1111/hiv.12206

PubMed Abstract | CrossRef Full Text | Google Scholar

28. Wang JM, Cheng YQ, Shi L, Ying RS, Wu XY, Li GY, et al. KLRG1 Negatively regulates natural killer cell functions through the akt pathway in individuals with chronic hepatitis C virus infection. J Virol. (2013) 87:11626–36. doi: 10.1128/JVI.01515-13

PubMed Abstract | CrossRef Full Text | Google Scholar

29. Müller-Durovic B, Lanna A, Polaco Covre L, Mills RS, Henson SM, Akbar AN. Killer cell lectin-like receptor G1 inhibits NK cell function through activation of adenosine 5′-monophosphate-activated protein kinase. J Immunol. (2016) 197:2891–9. doi: 10.4049/jimmunol.1600590

PubMed Abstract | CrossRef Full Text | Google Scholar

30. Herndler-Brandstetter D, Ishigame H, Shinnakasu R, Plajer V, Stecher C, Zhao J, et al. KLRG1+effector CD8+T cells lose KLRG1, differentiate into all memory T cell lineages, and convey enhanced protective immunity. Immunity (2018) 48:716–29.e8. doi: 10.1016/j.immuni.2018.03.015

PubMed Abstract | CrossRef Full Text | Google Scholar

31. Henson SM, Macaulay R, Riddell NE, Nunn CJ, Akbar AN. Blockade of PD-1 or p38 MAP kinase signaling enhances senescent human CD8+ T-cell proliferation by distinct pathways. Eur J Immunol. (2015) 45:1441–51. doi: 10.1002/eji.201445312

PubMed Abstract | CrossRef Full Text | Google Scholar

32. von Zglinicki T, Saretzki G, Ladhoff J, d'Adda di Fagagna F, Jackson SP. Human cell senescence as a DNA damage response. Mech Ageing Dev. (2005) 126:111–7. doi: 10.1016/j.mad.2004.09.034

PubMed Abstract | CrossRef Full Text | Google Scholar

33. Henson SM. Reversal of functional defects in highly differentiated young and old CD 8 T cells by PDL blockade. Immunology (2011) 135:355–63. doi: 10.1111/j.1365-2567.2011.03550.x

CrossRef Full Text

34. Lanna A, Gomes DCO, Muller-Durovic B, McDonnell T, Escors D, Gilroy DW, et al. A sestrin-dependent Erk-Jnk-p38 MAPK activation complex inhibits immunity during aging. Nat Immunol. (2017) 18:354–63. doi: 10.1038/ni.3665

PubMed Abstract | CrossRef Full Text | Google Scholar

35. Bacellar O, Lessa H, Schriefer A, Machado P, De Jesus AR, Dutra WO, et al. Up-regulation of Th1-type responses in mucosal leishmaniasis patients. Infect Immun. (2002) 70:6734–40. doi: 10.1128/IAI.70.12.6734-6740.2002

PubMed Abstract | CrossRef Full Text | Google Scholar

36. Antonelli LR, Dutra WO, Almeida RP, Bacellar O, Carvalho EM, Gollob KJ. Activated inflammatory T cells correlate with lesion size in human cutaneous leishmaniasis. Immunol Lett. (2005) 101:226–30. doi: 10.1016/j.imlet.2005.06.004

PubMed Abstract | CrossRef Full Text | Google Scholar

37. Albareda MC, Olivera GC, Laucella SA, Alvarez MG, Fernandez ER, Lococo B, et al. Chronic human infection with Trypanosoma cruzi drives CD4+ T cells to immune senescence. J Immunol. (2009) 183:4103–8. doi: 10.4049/jimmunol.0900852

PubMed Abstract | CrossRef Full Text | Google Scholar

38. Guimarães-Pinto K, Nascimento DO, Corrêa-Ferreira A, Morrot A, Freire-de-Lima CG, Lopes MF, et al. Trypanosoma cruzi infection induces cellular stress response and senescence-like phenotype in murine fibroblasts. Front Immunol. (2018) 9:1–11. doi: 10.3389/fimmu.2018.01569

PubMed Abstract | CrossRef Full Text | Google Scholar

39. Novais FO, Carvalho LP, Passos S, Roos DS, Carvalho EM, Scott P, et al. Genomic profiling of human Leishmania braziliensis lesions identifies transcriptional modules associated with cutaneous immunopathology. J Invest Dermatol. (2015) 135:94–101. doi: 10.1038/jid.2014.305

PubMed Abstract | CrossRef Full Text | Google Scholar

40. Báfica A, Oliveira F, Freitas LAR, Nascimento EG, Barral A. American Cutaneous Leishmaniasis unresponsive to antimonial drugs: successful treatment using combination of N-methilglucamine antimoniate plus pentoxifylline. Int J Dermatol. (2003) 42:203–7. doi: 10.1046/j.1365-4362.2003.01868.x

PubMed Abstract | CrossRef Full Text | Google Scholar

41. Lessa HA, Machado P, Lima F, Cruz ÁA, Bacellar O, Guerreiro J, et al. Successful treatment of refractory mucosal leishmaniasis with pentoxifylline plus antimony. Am J Trop Med Hyg. (2001) 65:87–9. doi: 10.4269/ajtmh.2001.65.87

PubMed Abstract | CrossRef Full Text | Google Scholar

42. Novais FO, Carvalho AM, Clark ML, Carvalho LP, Beiting DP, Brodsky IE, et al. CD8+T cell cytotoxicity mediates pathology in the skin by inflammasome activation and IL-1β production. PLoS Pathog. (2017) 13:1–21. doi: 10.1371/journal.ppat.1006196

PubMed Abstract | CrossRef Full Text | Google Scholar

43. Nasi M, De Biasi S, Gibellini L, Bianchini E, Pecorini S, Bacca V, et al. Ageing and inflammation in patients with HIV infection. Clin Exp Immunol. (2017) 187:44–52. doi: 10.1111/cei.12814

PubMed Abstract | CrossRef Full Text | Google Scholar

44. Da-Cruz AM, De Oliveira MP, De Luca PM, Mendonça SCF, Coutinho SG. Tumor necrosis factor-α in human American tegumentary leishmaniasis. Mem Inst Oswaldo Cruz (1996) 91:225–9. doi: 10.1590/S0074-02761996000200019

PubMed Abstract | CrossRef Full Text | Google Scholar

45. Nateghi Rostami M, Seyyedan Jasbi E, Khamesipour A, Miramin Mohammadi A. Plasma levels of tumor necrosis factor-alpha (TNF-α), TNF-α soluble receptor type 1 (sTNFR I) and IL-22 in human leishmaniasis. Trop Biomed. (2015) 32:478–84.

PubMed Abstract | Google Scholar

46. Sigmundsdóttir H, Gudjónsson JE, Jónsdóttir I, Lúdvíksson BR, Valdimarsson H. The frequency of CLA+CD8+ T cells in the blood of psoriasis patients correlates closely with the severity of their disease. Clin Exp Immunol. (2001) 126:365–9. doi: 10.1046/j.1365-2249.2001.01688.x

PubMed Abstract | CrossRef Full Text | Google Scholar

47. Antúnez C, Torres MJ, Mayorga C, Cornejo-García JA, Santamaría-Babi LF, Blanca M. Different cytokine production and activation marker profiles in circulating cutaneous-lymphocyte-associated antigen+ T cells from patients with acute or chronic atopic dermatitis. Clin Exp Allergy (2004) 34:559–66. doi: 10.1111/j.1365-2222.2004.1933.x

CrossRef Full Text | Google Scholar

48. Woodland DL, Kohlmeier JE. Migration, maintenance and recall of memory T cells in peripheral tissues. Nat Rev Immunol. (2009) 9:153–61. doi: 10.1038/nri2496

PubMed Abstract | CrossRef Full Text | Google Scholar

49. Costa RP, Gollob KJ, MacHado PRL, Bacellar OAR, Almeida RP, Barral A, et al. Adhesion molecule expression patterns indicate activation and recruitment of CD4+ T cells from the lymph node to the peripheral blood of early cutaneous leishmaniasis patients. Immunol Lett. (2003) 90:155–9. doi: 10.1016/j.imlet.2003.09.001

PubMed Abstract | CrossRef Full Text | Google Scholar

Keywords: cutaneous leishmaniasis, immunosenescence, inflammation, SASP-analogous, L. braziliensis, T cells

Citation: Covre LP, Martins RF, Devine OP, Chambers ES, Vukmanovic-Stejic M, Silva JA, Dietze R, Rodrigues RR, de Matos Guedes HL, Falqueto A, Akbar AN and Gomes DCO (2019) Circulating Senescent T Cells Are Linked to Systemic Inflammation and Lesion Size During Human Cutaneous Leishmaniasis. Front. Immunol. 9:3001. doi: 10.3389/fimmu.2018.03001

Received: 26 June 2018; Accepted: 04 December 2018;
Published: 04 January 2019.

Edited by:

Debora Decote-Ricardo, Universidade Federal Rural do Rio de Janeiro, Brazil

Reviewed by:

Salvador Iborra, Universidad Complutense de Madrid, Spain
Tatiana Rodrigues de Moura, Federal University of Sergipe, Brazil

Copyright © 2019 Covre, Martins, Devine, Chambers, Vukmanovic-Stejic, Silva, Dietze, Rodrigues, de Matos Guedes, Falqueto, Akbar and Gomes. 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: Arne N. Akbar, a.akbar@ucl.ac.uk
Daniel C. O. Gomes, dgomes@ndi.ufes.br

These authors have contributed equally to this work