Combined Analysis of Interleukin-10 Gene Polymorphisms and Protein Expression in Children With Cerebral Palsy

Abstract

Background:

Interleukin-10 (IL-10) is an important anti-inflammatory and immunosuppressive cytokine, and it has indispensable functions in both the onset and development of inflammatory disorders. The association between persistent inflammation and the development of cerebral palsy (CP) has attracted much attention.

Objective:

The purpose of this study was to investigate whether IL-10 gene polymorphisms and plasma protein expression are associated with CP and to analyze the role of IL-10 in CP.

Methods:

A total of 282 CP patients and 197 healthy controls were genotyped for IL-10 polymorphisms (rs1554286, rs1518111, rs3024490, rs1800871, and rs1800896). Among them, 95 CP patients and 93 healthy controls were selected for plasma IL-10 measurement.

Results:

The differences in the rs3024490 (p = 0.033) and rs1800871 (p = 0.033) allele frequencies of IL-10 were determined between CP patients and controls. The frequencies of allele and genotype between CP patients with spastic tetraplegia and normal controls of IL-10 polymorphisms showed significant differences for rs1554286, rs151811, rs3024490, rs1800871, and rs1800896 (p_allele = 0.015, 0.009, 0.006, 0.003, and 0.006, p_genotype = 0.039, 0.018, 0.027, 0.012, and 0.03, respectively). The plasma IL-10 protein level in CP patients was higher than normal controls (9.13 ± 0.77 vs. 6.73 ± 0.63 pg/ml, p = 0.017). IL-10 polymorphisms and protein association analysis showed that the TT genotype had higher plasma IL-10 protein levels compared to the GG + GT genotype at rs3024490 (11.14 ± 7.27 vs. 7.44 ± 6.95 pg/ml, p = 0.045, respectively) in CP cases.

Conclusion:

These findings provide an important contribution toward explaining the pleiotropic role of IL-10 in the complex etiology of CP.

Introduction

Cerebral palsy (CP) comprises a group of disorders affecting movement and posture due to non-progressive lesions or abnormalities in the immature brain, and these can lead to costly and life-long disability (1, 2). Studies have identified a number of risk factors for the development of CP. During the last decade, intrauterine infection and inflammation have been recognized as the most common causes of preterm delivery and white-matter brain injury such as periventricular leukomalacia (PVL) and subsequent development of CP (3–6). It is also known that the activation of inflammation plays a key role in the mechanisms of intrauterine infection-triggered brain damage (7, 8).

It is well known that the pro-inflammatory cytokine level in the amniotic fluid or in neonatal blood is directly related to the risk of developing CP (3, 9), and high levels of expression of TNFα, IL-1β, and IL-6 increase the risk for development of brain lesions with PVL (7, 10). IL-17 has also been reported to act synergistically with TNF and IL-1 and to play a notable role in inducing and mediating pro-inflammatory responses (11–13). These pro-inflammatory cytokines are responsible for initiating inflammation in response to tissue damage, while anti-inflammatory cytokines are released to limit the sustained or excessive inflammatory response (14). IL-10 is a main anti-inflammatory cytokine and has been suggested to play a crucial role in neuronal homeostasis and cell survival (15, 16). IL-10 plays a protective role in microglial cultures after a pro-inflammatory insult (17) and in rat pups born to dams infected with Escherichia coli (18). However, several studies have questioned the perception of IL-10 solely as an immunosuppressive cytokine because IL-10 can also stimulate immune responses by promoting the proliferation and cytotoxic activity of natural killer cells and CD8+ T-cells (19) as well as the survival, proliferation, differentiation, MHC class II expression, and antibody production of B-cells (20, 21). Increasing evidence indicates that IL-10 is involved in both the onset and development of inflammatory diseases. In a study of very low birth weight children suspected of having late-onset sepsis, the expression of the anti-inflammatory cytokines IL-4 and IL-10 was significantly elevated (22). Together, these studies indicate that the biological activity of IL-10 is variable and results in protective or pathogenic effects at different stages of disease and that IL-10 might play an important role in the pathogenesis of CP.

The protein expression of cytokines is regulated by genetic variants in the cytokine genes (15, 23), and accumulating evidence suggests that inherited cytokine single nucleotide polymorphisms (SNPs) contribute to increased risk of CP (24, 25). In following with this, it has been reported that SNPs within the coding and promoter regions of the IL-10 gene can affect the expression and secretion of this cytokine (26, 27). Considering the potential role of IL-10 in the etiology of CP, the present research sought to evaluate the possible association of IL-10 SNPs and IL-10 plasma levels with susceptibility to CP in a Chinese population.

Materials and Methods

Subjects

A total of 282 CP patients and 197 healthy controls were enrolled (Table 1). We collected all CP patients between 1 July 2010 and 31 May 2012 from the 3rd Affiliated Hospital of Zhengzhou University and Zhengzhou Children’s Hospital, which included 98 girls (34.8%) and 184 boys (65.2%) with a mean age ± SD of 16.2 ± 12.7 months. The diagnosis of CP patients was made by child neurologists according to the guidelines proposed by the Surveillance of CP in Europe network (28) through clinical examination or medical records, including brain imaging. The healthy controls [42 girls (21.3%) and 155 boys (78.7%) with a mean age ± SD of 24.0 ± 16.4 months] were enrolled during their physical examination from the same hospitals. Of these, 95 CP patients (56 boys and 39 girls) and 93 healthy controls (78 boys and 15 girls) were selected for the assay of IL-10 protein level (Table 2), and the mean age ± SD was 20.8 ± 14.4 and 21.6 ± 13.8 months, respectively. All subjects were Han Chinese as reported by their parents. All of the subjects, including both CP patients and controls, with myopathy, metabolic anomalies, or infections were excluded because of the genetic and familial factors that are associated with CP. Approval for the study was obtained from the ethics committee of Zhengzhou University in accordance with the Helsinki Declaration (201002006). Written informed consent was obtained from at least one of the parents after fully explaining the procedure.

The clinical data were stratified by the type of CP, birth asphyxia, and complications such as PVL and hypoxic–ischemic encephalopathy. The criteria for these risk factors were as previously described (28).

Sample Collection

The blood samples were taken by skilled nurses. EDTA was routinely used as the anti-coagulant in the study. The samples were separated by centrifugation (1,500 × g for 15 min) at 21°C within 2 h after being collected. The plasma was obtained from the supernatant, and DNA was obtained from the remaining blood components in the same sample. All the fractions were stored at −80°C until use. All methods were performed in accordance with the relevant guidelines and regulations.

Polymorphism Selection

Five SNPs (rs1554286, rs1518111, rs3024490, rs1800871, and rs1800896) of the IL-10 gene whose minor allele frequencies in the Chinese Han population are more than 0.1 were selected from the dbSNP database¹ and the HapMap human SNP database.² The rs1554286 (intron 3), rs1518111 (intron 2), and rs3024490 (intron 1) SNPs are located in the coding region of IL-10, and the rs1800871 and rs1800896 SNPs are located in the upstream promoter region.

Genotyping

After collecting the plasma, the AxyPrep Blood Genomic DNA Miniprep Kit (Axygen Biosciences, Union City, CA, USA) was used for preparing genomic DNA from the remaining blood components by following the manufacturer’s protocol. After the amplification of SNP-spanning fragments by multiplex PCR, the SNPs were genotyped on the Sequenom MassARRAY SNP genotyping platform (Sequenom, San Diego, CA, USA). The probes and primers were designed by the SEQUENOM online tools.³ The genotype results were analyzed by a person who was blinded to the clinical data.

Cytokine Protein Level Measurement

The plasma samples for IL-10 protein analysis were thawed completely at room temperature, mixed by vortexing, and centrifuged at 1,500 × g for 15 min to collect the supernatants for the subsequent cytokine assay. A Milliplex Human Cytokine/Chemokine kit (IL-10, IL-17 IL-6, IL-8, TNF-α, and IFN-γ) was used with the Multiplex Cytokine Assay (Millipore, Billerica, MA, USA). Quality controls were performed in parallel between the plates using reagents provided in the kits. Data were acquired on a Luminex 200IS System (Luminex Corporation, Austin, TX, USA). There was a 6.94% plate variation in this assay, and the detection limit was 0.3 pg/mL. The samples with cytokine levels below the limit of detection were excluded. IL-10 levels were expressed as picograms per milliliter.

Statistical Analysis

All gene analyses, including Hardy–Weinberg equilibrium tests, comparison of allele and genotype frequency, calculation of odd ratios and 95% confidence interval (95% CIs), estimation of pairwise linkage disequilibrium (LD), and haplotype association analysis were conducted with the SHEsis online software platform.⁴ The program SNPSpD,⁵ which takes marker LD information into consideration, was used to correct for multiple testing performed on each individual SNP. For IL-10 analysis, Student’s unpaired t-test was used. The Mann–Whitney U-test was used for the data with unequal variances. Statistical analyses were performed with SPSS (version 19.0) and Graphpad Prism 6.0 (Graphpad, La Jolla, CA, USA). All reported p-values were two-tailed, and statistical significance was set at p < 0.05.

Results

Association of IL-10 Gene Polymorphisms With the Total Group With CP

To examine the association between CP and the polymorphisms in the IL-10 gene, we detected genotype and allele frequencies of five SNPs in the 282 CP patients and the 197 healthy controls. The frequencies and analytic results for the SNPs are presented in Table 3. The genotypic distribution of the five selected SNPs of IL-10 in the normal controls was in Hardy–Weinberg equilibrium. In the analysis of allele frequencies, differences between the total CP patients (n = 282) and normal controls (n = 197) for rs3024490 (p = 0.011, after SNPSpD correction, p = 0.033) and rs1800871 (p = 0.011, after SNPSpD correction, p = 0.033) were observed. There was also strong LD between rs3024490 and rs1800871 (r² = 0.955) (Table 4), which makes it reasonable to have the same p-value for rs3024490 and rs1800871.

Association of IL-10 Gene Polymorphisms With the Subgroups of CP

Because CP is a complex syndrome with multiple etiological factors involved in disease pathogenesis, we performed subgroup analysis of IL-10 SNPs according to subtypes of CP, birth complications, and maternal factors. The frequencies of allele and genotype were different between CP patients with spastic tetraplegia (n = 123) and normal controls (n = 197) for rs1554286, rs151811, rs3024490, rs1800871, and rs1800896 (p_allele = 0.015, 0.009, 0.006, 0.003, and 0.006, respectively, after the SNPSpD correction), but no other significant differences were found when comparing allele and genotype distributions of these five SNPs between other CP subgroups and controls (Table 5).

Cytokine Analysis

The plasma IL-10 protein level was increased significantly in CP patients compared to normal controls (9.13 ± 7.07 vs. 6.79 ± 5.63 pg/ml, respectively, p = 0.017) (Figure 1A). The subgroup analysis showed that the plasma IL-10 level was also increased in the CP patients with spastic tetraplegia compared to the controls (9.86 ± 6.00 vs. 6.79 ± 5.63 pg/ml, respectively, p = 0.044) (Figure 1B). There were no significant differences in plasma IL-10 protein levels in other subgroup analyses.

Figure 1

Association of the SNPs With Cytokine Production

To confirm whether the IL-10 gene is linked with CP susceptibility, we further analyzed the relationship between genotypes of two SNPs associated with CP and plasma IL-10 protein levels. The results showed that the TT genotype had higher plasma IL-10 protein levels compared to the GG + GT genotype at rs3024490 (11.14 ± 7.27 vs. 7.44 ± 6.95 pg/ml, respectively, p = 0.045) (Figure 2A), and rs1800871 showed a tendency of high IL-10 protein level in the TT genotype compared to the CC + CT genotype (10.82 ± 7.33 vs. 7.62 ± 6.96 pg/ml, respectively, p = 0.079) in CP cases (Figure 2B), whereas no association was found for either SNP in controls. Although IL-10 is produced by constitutive or inducible expression, these results indicated that the genotypes of rs3024490 might play a more important role in the induced expression of IL-10.

Figure 2

Discussion

It has been accepted that inflammation plays an important role in the brain during the perinatal period and might contribute to the development of CP (23). Several studies have reported that increased pro-inflammatory cytokines such as IL-1β, IL-6, TNFα, and IL-8 in cord blood or amniotic fluid are associated with CP (23, 29), and IL-6 protein levels are higher in the blood (28) and cerebrospinal fluid of CP patients (30). Moreover, the balance between the levels of pro-inflammatory and anti-inflammatory cytokines determines the effect of the inflammatory responses.

IL-10 function is complicated and can have both stimulatory and inhibitory effects on different types of immune responses. IL-10 can strongly inhibit the secretion of IL-2/IFN-γ by TH1 cells, and it inhibits the secretion of IL-1, IL-6, IL-12, and tumor necrosis factor in macrophages and dendritic cells in order to reduce tissue damage (31, 32). IL-10, as a potential anti-inflammatory cytokine, creates favorable conditions for the persistence of microbes and chronic diseases (33), both of which are involved in clinical perinatal brain damage (15). It has been reported that the upregulation of IL-10 after injury might have anti-inflammatory effects in specific regions of the immature brain in the postnatal rat brain infection model (34), and anatomical characteristics have been associated with functional findings in athetotic-type and spastic-type CP using an atlas-based analysis (35). In the current study, we found that IL-10 protein levels were increased in CP patients, especially in spastic tetraplegia, the most severe subtype of CP patients. The predominantly negative immune regulatory functions of IL-10 can play a critical role in mediating T-cell functional exhaustion, which makes these cells detrimental in chronic infection (36). Prolonged microglial reactivity and increased cytokine expression have been noted in animal models of traumatic brain injury, and altered inflammatory responses have been shown to persist for at least 7 years after brain damage in CP patients (37). This suggests that one reason for why the plasma IL-10 level increases in CP patients is the inability for the body to clear antigen, which leads to repetitive antigen stimulation and IL-10 induction in a manner similar to chronic infection. In other words, the high plasma IL-10 level might be an attempt by the immune response to counterbalance the expression of pro-inflammatory cytokines (38). Our present results support the hypothesis that inflammation triggers an inadequate immunological response in preterm infants with a consequently increased risk of CP. The cytokines, as indicators of inflammation, usually have a half-life of only a few hours, whereas previous studies (3, 7, 9, 10, 23, 29) and our study have shown persistent inflammation in CP patients. Therefore, it is possible that the inflammatory process in the brain is continuously being activated after perinatal brain injury, and future studies should focus on the dynamic changes in neuroinflammation and how these changes relate to the progression of CP.

Gene polymorphism studies suggest the involvement of as yet unidentified linkages between allelic variants and the pathogenesis of disease (39), and SNPs in genes encoding cytokines and their receptors have been implicated in both increased and decreased risk of perinatal brain injury (23). Studies have suggested that IL-6, IL-8, and TNF-α SNPs (40, 41) might predispose to CP because an increased risk for CP has been shown to be positively associated with the increased production of these proteins, but nothing has been known about the relationship between IL-10 SNPs and CP.

The human IL-10 gene is located on chromosome 1q31–1q32 and is composed of four introns and five exons (42). Three SNPs in the IL-10 intron region (rs1554286, rs1518111, and rs3024490) have been reported to be associated with risk for ischemic stroke and idiopathic recurrent miscarriage (43–45), and two SNPs in the IL-10 promoter region (rs1800871 and rs1800896) have been identified as highly polymorphic risk factors for systemic sclerosis (46) and Alzheimer’s disease (47). These five SNPs are in strong LD, and this is believed to have biological significance (39). In the current study, all five SNPs were associated with tetraplegia CP patients. In addition, reports have also shown that the upregulation of IL-10 after injury might have anti-inflammatory effects in distinct anatomic sites in the postnatal rat brain infection model (34), and anatomical characteristics have been delineated with functional findings in athetotic-type and spastic-type CP using the atlas-based analysis (35). In this study, we found the TT genotype frequency in the CP group to be higher than the control group and the TT genotype of rs3024490 and rs1800871 seems to be related to higher circulating levels of IL-10 protein in CP patients but not in controls. These results suggest that the genotype TT of rs3024490 associated an increased IL-10 expression might be due to the different reactivity of genetic variants to risk factors for CP (48, 49). Therefore, we hypothesize that cytokines affect different regions of the developing brain and that the subtypes of CP are determined by the functional genotypes of IL-10 in the development of CP. Thus this group of children should be paid more attention to, especially in early life before clinical symptoms of CP begin to appear, which is exactly where the significance of the present study lies. However, we need to expand the sample size in subsequent experiments in order to test this hypothesis.

Cerebral palsy is a heterogeneous disease with complex interactions between genetic influences and environmental influences. Understanding the genes and gene–environment interactions in CP and the underlying cytokine-related mechanisms might lead to the development of new preventive and therapeutic strategies for CP. In summary, this study suggests that IL-10 SNPs are strongly associated with CP through the regulation of IL-10 gene function that leads to altered IL-10 production. Future work should focus on the interactions between genetic and cytokine-related mechanisms in the pathogenesis of CP. A better understanding of the potentially beneficial and detrimental roles of IL-10 in CP might not only help improve our understanding of CP pathogenesis, but might also help develop novel strategies for the prevention of CP.

References

• 1

  StoknesMAndersenGLElkamilAIIrgensLMSkranesJSalvesenKAet alThe effects of multiple pre- and perinatal risk factors on the occurrence of cerebral palsy. A Norwegian register based study. Eur J Paediatr Neurol (2012) 16(1):56–63.10.1016/j.ejpn.2011.10.004

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 2

  YoonBHRomeroRParkJSKimCJKimSHChoiJHet alFetal exposure to an intra-amniotic inflammation and the development of cerebral palsy at the age of three years. Am J Obstet Gynecol (2000) 182(3):675–81.10.1067/mob.2000.104207

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 3

  Kapitanovic VidakHCatela IvkovicTJokicMSpaventiRKapitanovicS. The association between proinflammatory cytokine polymorphisms and cerebral palsy in very preterm infants. Cytokine (2012) 58(1):57–64.10.1016/j.cyto.2011.12.018

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 4

  RezaiePDeanA. Periventricular leukomalacia, inflammation and white matter lesions within the developing nervous system. Neuropathology (2002) 22(3):106–32.10.1046/j.1440-1789.2002.00438.x

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 5

  BashiriABursteinEMazorM. Cerebral palsy and fetal inflammatory response syndrome: a review. J Perinat Med (2006) 34(1):5–12.10.1515/JPM.2006.001

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 6

  BackSARiddleAMcClureMM. Maturation-dependent vulnerability of perinatal white matter in premature birth. Stroke (2007) 38(2 Suppl):724–30.10.1161/01.STR.0000254729.27386.05

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 7

  YoonBHJunJKRomeroRParkKHGomezRChoiJHet alAmniotic fluid inflammatory cytokines (interleukin-6, interleukin-1beta, and tumor necrosis factor-alpha), neonatal brain white matter lesions, and cerebral palsy. Am J Obstet Gynecol (1997) 177(1):19–26.10.1016/S0002-9378(97)70432-0

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 8

  YounYAKimSJSungIKChungSYKimYHLeeIG. Serial examination of serum IL-8, IL-10 and IL-1Ra levels is significant in neonatal seizures induced by hypoxic-ischaemic encephalopathy. Scand J Immunol (2012) 76(3):286–93.10.1111/j.1365-3083.2012.02710.x

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 9

  DugganPJMaaloufEFWattsTLSullivanMHCounsellSJAllsopJet alIntrauterine T-cell activation and increased proinflammatory cytokine concentrations in preterm infants with cerebral lesions. Lancet (2001) 358(9294):1699–700.10.1016/S0140-6736(01)06723-X

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 10

  KadhimHTabarkiBVerellenGDe PrezCRonaAMSebireG. Inflammatory cytokines in the pathogenesis of periventricular leukomalacia. Neurology (2001) 56(10):1278–84.10.1212/WNL.56.10.1278

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 11

  ChiricozziAGuttman-YasskyESuarez-FarinasMNogralesKETianSCardinaleIet alIntegrative responses to IL-17 and TNF-alpha in human keratinocytes account for key inflammatory pathogenic circuits in psoriasis. J Invest Dermatol (2011) 131(3):677–87.10.1038/jid.2010.340

  • CrossRef
  • Google Scholar

• 12

  MiossecPKornTKuchrooVK. Interleukin-17 and type 17 helper T cells. N Engl J Med (2009) 361(9):888–98.10.1056/NEJMra0707449

  • CrossRef
  • Google Scholar

• 13

  BettelliEOukkaMKuchrooVK. T(H)-17 cells in the circle of immunity and autoimmunity. Nat Immunol (2007) 8(4):345–50.10.1038/ni0407-345

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 14

  SultaniMStringerAMBowenJMGibsonRJ. Anti-inflammatory cytokines: important immunoregulatory factors contributing to chemotherapy-induced gastrointestinal mucositis. Chemother Res Pract (2012) 2012:490804.10.1155/2012/490804

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 15

  DammannOO’SheaTM. Cytokines and perinatal brain damage. Clin Perinatol (2008) 35(4):643–63.10.1016/j.clp.2008.07.011

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 16

  StrleKZhouJHShenWHBroussardSRJohnsonRWFreundGGet alInterleukin-10 in the brain. Crit Rev Immunol (2001) 21(5):427–49.10.1615/CritRevImmunol.v21.i5.20

  • CrossRef
  • Google Scholar

• 17

  KremlevSGPalmerC. Interleukin-10 inhibits endotoxin-induced pro-inflammatory cytokines in microglial cell cultures. J Neuroimmunol (2005) 162(1–2):71–80.10.1016/j.jneuroim.2005.01.010

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 18

  Rodts-PalenikSWyatt-AshmeadJPangYThigpenBCaiZRhodesPet alMaternal infection-induced white matter injury is reduced by treatment with interleukin-10. Am J Obstet Gynecol (2004) 191(4):1387–92.10.1016/j.ajog.2004.06.093

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 19

  RowbottomAWLepperMAGarlandRJCoxCVCorleyEG. Interleukin-10-induced CD8 cell proliferation. Immunology (1999) 98(1):80–9.10.1046/j.1365-2567.1999.00828.x

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 20

  RoussetFGarciaEDefranceTPeronneCVezzioNHsuDHet alInterleukin 10 is a potent growth and differentiation factor for activated human B lymphocytes. Proc Natl Acad Sci U S A (1992) 89(5):1890–3.10.1073/pnas.89.5.1890

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 21

  MaCSHareNJNicholsKEDupreLAndolfiGRoncaroloMGet alImpaired humoral immunity in X-linked lymphoproliferative disease is associated with defective IL-10 production by CD4+ T cells. J Clin Invest (2005) 115(4):1049–59.10.1172/JCI200523139

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 22

  NgPCLiKWongRPChuiKWongELiGet alProinflammatory and anti-inflammatory cytokine responses in preterm infants with systemic infections. Arch Dis Child Fetal Neonatal Ed (2003) 88(3):F209–13.10.1136/fn.88.3.F209

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 23

  McAdamsRMJuulSE. The role of cytokines and inflammatory cells in perinatal brain injury. Neurol Res Int (2012) 2012:561494.10.1155/2012/561494

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 24

  GibsonCSMacLennanAHGoldwaterPNHaanEAPriestKDekkerGA. The association between inherited cytokine polymorphisms and cerebral palsy. Am J Obstet Gynecol (2006) 194(3):.e1–11.10.1016/j.ajog.2006.01.093

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 25

  GibsonCSMaclennanAHDekkerGAGoldwaterPNSullivanTRMunroeDJet alCandidate genes and cerebral palsy: a population-based study. Pediatrics (2008) 122(5):1079–85.10.1542/peds.2007-3758

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 26

  LiNZhuQLiZHanQZhangGChenJet alIL17A gene polymorphisms, serum IL-17A and IgE levels, and hepatocellular carcinoma risk in patients with chronic hepatitis B virus infection. Mol Carcinog (2014) 53(6):447–57.10.1002/mc.21992

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 27

  DordelmannMKerkJDresslerFBrinkhausMJBartelsDBDammannCEet alInterleukin-10 high producer allele and ultrasound-defined periventricular white matter abnormalities in preterm infants: a preliminary study. Neuropediatrics (2006) 37(3):130–6.10.1055/s-2006-924554

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 28

  BiDChenMZhangXWangHXiaLShangQet alThe association between sex-related interleukin-6 gene polymorphisms and the risk for cerebral palsy. J Neuroinflammation (2014) 11(1):100.10.1186/1742-2094-11-100

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 29

  GirardSKadhimHRoyMLavoieKBrochuMELaroucheAet alRole of perinatal inflammation in cerebral palsy. Pediatr Neurol (2009) 40(3):168–74.10.1016/j.pediatrneurol.2008.09.016

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 30

  AhlinKHimmelmannKHagbergGKacerovskyMCoboTWennerholmUBet alCerebral palsy and perinatal infection in children born at term. Obstet Gynecol (2013) 122(1):41–9.10.1097/AOG.0b013e318297f37f

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 31

  HwangWLeeCGLeeCVermaRRudraDParkZYet alLocus-specific reversible DNA methylation regulates transient IL-10 expression in Th1 cells. J Immunol (2018) 200(5):1865–75.10.4049/jimmunol.1701162

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 32

  ImSHHueberAMonticelliSKangKHRaoA. Chromatin-level regulation of the IL10 gene in T cells. J Biol Chem (2004) 279(45):46818–25.10.1074/jbc.M401722200

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 33

  AmbalavananNCarloWAMcDonaldSADasASchendelDEThorsenPet alCytokines and posthemorrhagic ventricular dilation in premature infants. Am J Perinatol (2012) 29(9):731–40.10.1055/s-0032-1316443

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 34

  GonzalezPBurgayaFAcarinLPeluffoHCastellanoBGonzalezB. Interleukin-10 and interleukin-10 receptor-I are upregulated in glial cells after an excitotoxic injury to the postnatal rat brain. J Neuropathol Exp Neurol (2009) 68(4):391–403.10.1097/NEN.0b013e31819dca30

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 35

  YoshidaSFariaAVOishiKKandaTYamoriYYoshidaNet alAnatomical characterization of athetotic and spastic cerebral palsy using an atlas-based analysis. J Magn Reson Imaging (2013) 38(2):288–98.10.1002/jmri.23931

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 36

  BlackburnSDWherryEJ. IL-10, T cell exhaustion and viral persistence. Trends Microbiol (2007) 15(4):143–6.10.1016/j.tim.2007.02.006

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 37

  FleissBGressensP. Tertiary mechanisms of brain damage: a new hope for treatment of cerebral palsy?Lancet Neurol (2012) 11(6):556–66.10.1016/S1474-4422(12)70058-3

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 38

  MooreKWde Waal MalefytRCoffmanRLO’GarraA. Interleukin-10 and the interleukin-10 receptor. Annu Rev Immunol (2001) 19:683–765.10.1146/annurev.immunol.19.1.683

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 39

  RezaeiNAghamohammadiAMahmoudiMShakibaYKardarGAMoradiBet alAssociation of IL-4 and IL-10 gene promoter polymorphisms with common variable immunodeficiency. Immunobiology (2010) 215(1):81–7.10.1016/j.imbio.2009.01.011

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 40

  ChenMLiTLinSBiDZhuDShangQet alAssociation of interleukin 6 gene polymorphisms with genetic susceptibilities to spastic tetraplegia in males: a case-control study. Cytokine (2013) 61(3):826–30.10.1016/j.cyto.2013.01.011

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 41

  DjukicMGibsonCSMaclennanAHGoldwaterPNHaanEAMcMichaelGet alGenetic susceptibility to viral exposure may increase the risk of cerebral palsy. Aust N Z J Obstet Gynaecol (2009) 49(3):247–53.10.1111/j.1479-828X.2009.00999.x

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 42

  DongYChenSJYuJL. A systematic review and meta-analysis of long-term development of early term infants. Neonatology (2012) 102(3):212–21.10.1159/000338099

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 43

  XieGMyintPKZamanMJLiYZhaoLShiPet alRelationship of serum interleukin-10 and its genetic variations with ischemic stroke in a Chinese general population. PLoS One (2013) 8(9):e74126.10.1371/journal.pone.0074126

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 44

  ParkHKKimDHYunDHBanJY. Association between IL10, IL10RA, and IL10RB SNPs and ischemic stroke with hypertension in Korean population. Mol Biol Rep (2013) 40(2):1785–90.10.1007/s11033-012-2232-5

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 45

  QaddourahRHMagdoudKSaldanhaFLMahmoodNMustafaFEMahjoubTet alIL-10 gene promoter and intron polymorphisms and changes in IL-10 secretion in women with idiopathic recurrent miscarriage. Hum Reprod (2014) 29(5):1025–34.10.1093/humrep/deu043

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 46

  PengWJWangBXPanHFTaoJHZhangJQHeQet alAssociation of the interleukin-10 1082G/A, 819C/T and 3575T/A gene polymorphisms with systemic sclerosis: a meta-analysis. Mol Biol Rep (2012) 39(6):6851–5.10.1007/s11033-012-1510-6

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 47

  ZhangYZhangJTianCXiaoYLiXHeCet alThe -1082G/A polymorphism in IL-10 gene is associated with risk of Alzheimer’s disease: a meta-analysis. J Neurol Sci (2011) 303(1–2):133–8.10.1016/j.jns.2010.12.005

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 48

  O’CallaghanMEMaclennanAHGibsonCSMcMichaelGLHaanEABroadbentJLet alFetal and maternal candidate single nucleotide polymorphism associations with cerebral palsy: a case-control study. Pediatrics (2012) 129(2):e414–23.10.1542/peds.2011-0739

  • Pubmed Abstract
  • CrossRef
  • Google Scholar

• 49

  LiangYXuWDZhangMQiuLJNiJWangXSet alMeta-analysis of association between cytokine gene polymorphisms and Behcet’s disease risk. Int J Rheum Dis (2013) 16(6):616–24.10.1111/1756-185X.12221

  • Pubmed Abstract
  • CrossRef
  • Google Scholar