|Year : 2015 | Volume
| Issue : 2 | Page : 49-54
Effects of interleukin-10 gene polymorphism on clinical diversity and activity of systemic lupus erythematosus
Ahmad A Emerah MD 1, Kamal F Mohamed2, Nisreen E Elbadawy2, Mai H Rashad2
1 Department of Rheumatology and Rehabilitation, Faculty of Medicine, Zagazig University, Zagazig, Egypt
2 Department of Medical Microbiology and Immunology, Faculty of Medicine, Zagazig University, Zagazig, Egypt
|Date of Submission||04-Jan-2015|
|Date of Acceptance||07-Apr-2015|
|Date of Web Publication||29-May-2015|
Dr. Ahmad A Emerah
Zagaig University Hospitals, Rheumatology and Rehablitation Department, Sharkia
Source of Support: None, Conflict of Interest: None
This study was carried out to determine the effects of interleukin (IL)-10 gene polymorphism 1082A/G on clinical diversity and activity of systemic lupus erythematosus (SLE), as it was shown to be associated with E26 transcription factor binding site, and to assess IL-10 concentration in SLE patients.
Patients and methods
Blood was drawn from 54 SLE patients and 27 healthy controls for DNA extraction. The single nucleotide polymorphism was identified using the PCR-restriction fragment length polymorphism, and serum sample was collected to assay IL-10 concentration.
There was an increase in IL-10 concentration in SLE total patients (mean 49.5 pg/ml). Mutant allele A (76.9%) was found more frequently in SLE patients compared with allele G (23.1%). Genotype AA (66.7%) was found more frequently, followed by AG (20.4%) and GG (12.9%).
IL-10 concentration was elevated in SLE patients and was shown to be associated with disease activity. IL-10 gene polymorphism is not a strong indicator to show susceptibility of the disease.
Keywords: interleukin-10, single nucleotide polymorphism, systemic lupus erythematosus
|How to cite this article:|
Emerah AA, Mohamed KF, Elbadawy NE, Rashad MH. Effects of interleukin-10 gene polymorphism on clinical diversity and activity of systemic lupus erythematosus. Egypt Rheumatol Rehabil 2015;42:49-54
|How to cite this URL:|
Emerah AA, Mohamed KF, Elbadawy NE, Rashad MH. Effects of interleukin-10 gene polymorphism on clinical diversity and activity of systemic lupus erythematosus. Egypt Rheumatol Rehabil [serial online] 2015 [cited 2019 Jun 16];42:49-54. Available from: http://www.err.eg.net/text.asp?2015/42/2/49/157855
| Introduction|| |
Systemic lupus erythematosus (SLE) is the prototypical autoimmune disease that is characterized by autoantibody production, complement activation, and immune complex deposition, leading to diverse clinical manifestations and target tissue damage  .
SLE can vary widely in its severity, both at onset and during its course; some patients may have very mild disease with mild symptoms and no serious organ involvement, whereas others may be very ill with a number of organs affected .
Cytokines have been suggested to be involved in the pathogenesis of SLE, as they are fundamental components in the regulation of immune response, intervening in both cellular and humoral responses  .
Interleukin (IL)-10 is a key immunoregulatory cytokine that can be produced by almost all leukocytes, including innate immune cells such as monocytes, macrophages, dendritic cells, mast cells, natural killer cells, eosinophils, and neutrophils, and adaptive immune cells such as Th1, Th2, Treg, Tr1, Th3, T cells, and B cells , .
The role of IL-10 in the pathogenesis of SLE is unknown, but the increased production of IL-10 in sporadic cases of SLE , and the clinical improvements in SLE patients resulting from administration of anti-IL-10 monoclonal antibody support a central role for IL-10 in the pathogenesis of SLE  .
The human IL-10 gene located on lq31-32 is a susceptible region for SLE  . The individual variation in IL-10 production may be due to the genotypic variations in the human IL-10 promoter. Three single nucleotide polymorphisms (SNPs) at 1082A/G, 819T/C, and 592A/C in the promoter region have been demonstrated  .
Our study was carried out to determine the effects of IL-10 gene polymorphism 1082A/G on clinical diversity and activity of SLE and to assess the IL-10 concentration in SLE patients.
| Patients and methods|| |
Eighty-one participants were selected in this study. They were divided into two groups: the control group and the systemic lupus patient group. The control group included 27 healthy participants (17 female and 10 male participants), whose ages ranged from 19 to 60 years (mean 31.3 years). They were clinically free from any disease and were not receiving any drugs.
The systemic lupus patient group included 54 systemic lupus patients (diagnosed according to the American Rheumatism Association Criteria for the Classification of SLE , ). Patients were divided on the basis of the Systemic Lupus Erythematosus Disease Activity Index (SLEDAI) score into two groups: SLE group I (mild and moderate cases), which included 27 patients whose SLEDAI score was less than 12, and SLE group II (severe cases), which included 27 patients whose SLEDAI score was 12 or greater  .
The nature of the present study was explained to all patients. Verbal and written consent was obtained from all patients and controls. Reserch protocol was approved by the Ethical Committee of faculty of medicine, Zagazig University.
All patients were subjected to the following investigations:
- Complete blood picture.
- Erythrocyte sedimentation rate using the Westergren method.
- C-reactive protein using the latex agglutination method.
- Autoantibodies measurement with antinuclear antibody (ANA) and anti-dsDNA.
- Kidney function tests including evaluation of creatinine and blood nitrogen urea (BUN), complete urine analysis, and protein/creatinine ratio.
Blood samples were collected from all participants in two tubes: a plain tube to obtain serum, and a sodium heparin anticoagulant tube for whole blood.
Serum samples were assayed for IL-10 concentration using Human IL-10 Immunoassay (R&D Minneapolis, Minnesota, USA). This assay uses the quantitative sandwich enzyme immunoassay technique (ELISA). A microplate precoated with a monoclonal antibody specific for IL-10 is used. IL-10 standards and samples are pipetted into the wells, and any IL-10 present is bound by the immobilized antibody. After washing away any unbound substances, an enzyme-linked monoclonal antibody specific for IL-10 is added to the wells. Following a wash to remove any unbound antibody enzyme reagent, a substrate solution is added to the wells and color develops in proportion to the amount of IL-10 bound in the initial step. The color development is stopped, and the intensity of the color is measured.
DNA extraction for PCR amplification
DNA extraction was performed on all blood specimens using Gene JET whole-blood genomic DNA purification mini kit (Qiagen, Hilden, Germany). The purified DNA was stored at −20°c for PCR amplification.
PCR reactions were all performed on DNA extracts using the PCR Gold Master Mix Kit (BIORON, Ludwigshafen, Rhein, German).
The primer pair specific for the IL-10 gene promoter as used in the study by Mavrothalassitis and Ghysdael  (Sigma, St. Louis, Missouri, USA) was selected.
A forward primer, whose sequence was 5¢-AAG ACA ACA CTA CTA AGG CTT CCT T-3¢ for genotyping of SNP in the promotor region of the human IL-10 gene (−1082G>A) to produce a segment of 584 bp, and a reverse primer, whose sequence was 5¢-TAA ATA TCC TCA AAG TTC C-3¢, were used. Reaction mixtures were subjected to 35 cycles of amplification: initial denaturation at 94°C for 5 min; denaturation at 95°C for 30 s; annealing at 45°C for 30 s; extention at 72°C for 1 min; and final extention for 7 min.
Restriction enzyme digestion of DNA
Eco NI (Thermo Scientific Fast Digest Enzyme; Thermo Scientific) (Thermo Scientific, Waltham, Massachusetts, USA) recognizes CCTNN^NNNAGG sites and cuts best at 37°C in 5-15 min.
Conventional agarose gel electrophoresis
Conventional agarose gel electrophoresis was performed using ethidium bromide and 100 bp step ladder as a marker to determine the band size of genotypes.
Statistical analyses were carried out using SPSS (version 19; SPSS Inc., Chicago, Illinois, USA) for Windows. Data were statistically described in terms of mean ± SD, range or frequencies, and percentages. The χ2 -test was used to compare qualitative variables. A t-test was used to compare two independent groups as regards quantitative variables. Spearman's correlation coefficient and the Kruskal-Wallis test were used to differentiate variables against each other positively or inversely. A P value of less than 0.05 was considered to be significant.
| Results|| |
The demographic data of SLE patients and controls are shown in [Table 1].
In our study we found that there was an increase in IL-10 concentration in SLE group I, SLE group II, and SLE total patients compared with that in controls ([Table 2]). Moreover, IL-10 concentration correlated directly to the scores of SLEDAI in SLE total patients ([Table 3]).
|Table 3 Correlation of interleukin-10 concentration with scores of Systemic Lupus Erythematosus Disease Activity Index|
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Mutant allele A was found more frequently in SLE patients compared with allele G. Genotype AA was found more frequently, followed by AG and GG ([Table 4] and [Table 5]).
|Table 4 Interleukin-10 promoter alleles' distribution in different studied groups|
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|Table 5 Interleukin-10 promoter genotypes distribution in different studied groups|
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Genotype AA and AG were found to be associated with higher IL-10 concentration compared with GG, which means that allele A is suspected to affect IL-10 production ([Table 6]).
|Table 6 Association of interleukin-10 promoter genotypes with interleukin-10 concentration|
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There was no significant association between IL-10 gene promoter and SLEDAI ([Figure 1]).
|Figure 1 Gel electrophoresis representing the restriction fragment length polymorphism patterns obtained following digestion with the restriction enzyme EcoNI. Lane 1 represents 100 bp ladder marker; lanes 2, 3, and 4 represent two bands of homozygous mutant alleles AA with size 278 and 306 bp; lane 5 represents three bands of heterozygous alleles AG with size 272, 306, and 317 bp; and lane 6 represents two bands of homozygous wild alleles GG with size 267 and 317 bp.|
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| Discussion|| |
SLE is a potentially severe autoimmune disease, which demonstrates variations in incidence, prevalence, disease activity, and prognosis based on race and ethnicity  . SLE is a chronic systemic disease with variable clinical presentation. The exact pathological mechanisms of SLE remains elusive, and the etiology of SLE is known to be multifactorial, involving genes, sex hormones, and environmental factors including sunlight, drugs, and infections  . This study included 81 participants, and 54 of them were suffering from SLE , . An overall 90% of SLE patients were female and 10% were male. This finding indicates that female sex is considered as one of the predisposing factors of the disease and that hormones contribute through unknown mechanisms to increase the prevalence of SLE among women. The X chromosome may contribute to increasing the severity of the disease, as the gene known to contribute to the pathogenesis of SLE is CD40, which is located on chromosome X  . In our study, the most frequent clinical manifestations among SLE patients were malar rash (80%), arthritis (75%), renal involvement (55%), and fever (50%), and the least frequent clinical variables were cranial nerve affection and organic brain syndrome (0% for both). Moreover, the laboratory findings among SLE patients according to SLEDAI showed positivity of ANA (100%) and anti-dsDNA (80%).
However, in a study by Akbarian et al.  , which was conducted in Iran, the prevalence of manifestations was as follows: musculoskeletal, 83.2%; renal, 75%; hematologic, 66.4%; cutaneous, 55%; neuropsychiatric, 23.4%; pulmonary, 21.5%; and cardiac, 17.2%. There were positive ANAs in 86.4% of cases and positive anti-DNA in 82.3% of cases. These differences in clinical and laboratory findings indicate that genetic and climatic factors may lead to different presentations of lupus.
Cytokines are important components of immune response and regulation, and play an active role in activating, differentiating, and maturing immune cells. An imbalance between proinflammatory cytokines such as IL-6, tumor necrosis factor (TNF)-α, and IL-1, and anti-inflammatory cytokines such as IL-10, IL-4, and IL-13 is a well-known characteristic of SLE. Cytokines are heavily integrated in T-cell and B-cell signaling systems, and abnormal proinflammatory cytokines levels, particularly ILs, interferons, and TNFs, are important hallmark in hyperactivity of lymphocytes  .
IL-10, primarily produced by monocytes and lymphocytes, is a multifunctional cytokine in immunoregulation and inflammation. It enhances B-cell proliferation, differentiation, and antibody production and thus plays a role in B-cell hyperactivity and in increasing production of autoantibodies in SLE. It also inhibits functions of T cells and antigen-presenting cells, which in SLE may contribute to impaired cell-mediated immunity  . In our study, there was an increase in IL-10 concentration in total SLE patients (mean ± SD 49.5 ± 79.8 pg/ml), and the difference was found to be statistically significant when compared with that of the control group (P = 0.012). Moreover, a higher concentration of IL-10 was found in SLE group II (severe cases), with a mean ± SD of 81 ± 104.2 pg/ml, compared with SLE group I (mild and moderate cases), which had a mean ± SD of 17.9 ± 7.7 pg/ml. On comparing SLE group I (mild and moderate cases) and SLE group II (severe cases), the difference was statistically highly significant (P = 0.003). We also found that there is a highly significant correlation (directly proportionate) between IL-10 concentration in SLE total patients and SLEDAI (r = 0.383). Other studies , found that IL-10 concentration in SLE patients was increased (P < 0.001) and correlated positively with SLEDAI. Another study by El-Sayed et al.  which was conducted in Egypt found that IL-10 concentration was higher in SLE patients than in controls, but did not reach the significant level. The overproduced IL-10 in SLE patients may be ascribed to B cells and monocytes , . Moreover, B-cell secretion of IL-10 could regulate dendritic cells and T-cell function to promote Th2 cell deviation of the immune response  . Moreover, the enhanced excretion of IL-10 may be due to an increasing number of the earlier peripheral B-cell abnormalities including plasma cell expansion  .
In our study, we found that in SLE group I (mild and moderate cases) the IL-10 concentration was increased, but negatively correlated with SLEDAI (r = −0.046). Arora et al.  also reported that IL-10 concentration was higher in SLE patients than in controls, but negatively associated with SLEDAI scores. Other studies , found that there was no difference in serum IL-10 level between patients and controls. These conflicts may arise probably from several potential factors such as sample size, patients with different demographics, clinical characteristics, or types of therapy. In addition, in some indices measured for SLE activity, qualitative data with high heterogenecity between studies can also contribute to this discordance.
The human IL-10 gene that is located on chromosome 1q31-32 is a susceptible region for SLE. The individual variation in IL-10 production may be due to the genotypic variations in the human IL-10 promoter  . The 1082A/G polymorphism is located at putative regulatory regions in the promoter of the IL-10 gene  . As regards IL-10 gene 1082A/G polymorphism, in our study, we found that the mutant allele A (76.9%) was found more frequently compared with allele G (23.1%) in SLE total patients. Moreover, genotype AA distribution was found more frequently in SLE total patients (66.7%), followed by genotype AG (20.4%) and GG (12.9%). A study conducted on the southern Chinese population by Mok et al.  found that the frequency of allele A was 96% and that of allele G was 4%. A study conducted in Malaysia by Hee et al.  found that the frequency of allele A was 91% and that of allele G was 9% with genotype frequency (AA, 81.82%; AG, 18.18%; and GG, 0%). Other studies reported that there is a significant association with allele G and SLE risk, as reported in studies conducted in Poland by Sobkowiak et al.  , in Vietnam by Khoa et al.  and in Sweden by Fei et al.  . Another study  showed that the IL-10 G allele was associated with Asian but not with White SLE patients. However, no association was observed between 1082A/G and SLE patients in other studies , . These distinctions between the effects of the 1082A/G polymorphism in SLE risk may result from genetic heterogenecity, ethnicity, different exposure to environmental factors, and different sample size of population.
In our study we also found that there was an increase in IL-10 concentration in association with genotype AA in SLE patients, especially in SLE group I (mild and moderate cases), which was more significant (P = 0.022). However, in SLE group II (severe cases) there was no statistically significant association (P = 0.296), but genotype AA was more associated with increased IL-10 concentration compared with AG and GG ([Table 6]). In SLE total patients there was a statistically significant association of genotype AA with IL-10 concentration (P = 0.029). The SNP 1082 was considered to be in the proximal end of the IL-10 promoter, upstream of the transcription start site. It has been shown to be associated with the transcription binding site, which in turn may affect the production of IL-10  .
In our study when we compared IL-10 gene promoter genotype with SLEDAI, we found no relation or association. López et al.  stated that increased circulating levels of IL-10 have been reported in patients with SLE. However, there were no definitive data on the association of IL-10 polymorphisms and SLEDAI, probably due to heterogenecity of the disease.
| Conclusion|| |
From this study we conclude that IL-10 concentration is elevated in SLE patients and is shown to be associated with disease activity, and so it can be selected as a biomarker of the disease. IL-10 gene polymorphism 1082A/G is not a strong indicator to show susceptibility of the disease. Allele A is suspected to affect IL-10 production more than allele G.
Further studies with large sample size to provide us with a sufficient data to help in gene study are needed to confirm these findings. A study should be performed on gene haplotype frequencies in SLE patients, as it may have a role in disease susceptibility. Moreover, there could be some other uncovered mechanisms involved in the susceptibility to SLE. Therefore, further studies are needed to explore the exact mechanism. Other studies should be performed on other cytokines and their receptors such as IL-6, IL-4, TNF, TGF, and interferon to assess their role in the pathogenesis of the disease.
| Acknowledgements|| |
Conflicts of interest
There are no conflicts of interest.
| References|| |
Helmick CG, Felson DT, Lawrence RC, Gabriel S, Hirsch R, Kwoh CK, et al
. National Arthritis Data Workgroup. Estimates of the prevalence of arthritis and other rheumatic conditions in the United States. Part I. Arthritis Rheum 2008; 58
Miettunen PM, Ortiz-Alvarez O, Petty RE, Cimaz R, Malleson PN, Cabral DA, et al
. Gender and ethnic origin have no effect on longterm outcome of childhood-onset systemic lupus erythematosus. J Rheumatol 2004; 31
Mellor-Pita S, Citores MJ, Castejon R, Tutor-Ureta P, Yebra-Bango M, Andreu JL, Vargas JA. Decrease of regulatory T cells in patients with systemic lupus erythematosus. Ann Rheum Dis 2006; 65
Rhodes KA, Andrew EM, Newton DJ, Tramonti D, Carding SR. A subset of IL-10-producing gammadelta T cells protect the liver from Listeria-elicited, CD8(+) T cell-mediated injury. Eur J Immunol 2008; 38
Yanaba K, Bouaziz JD, Matsushita T, Tsubata T, Tedder TF. The development and function of regulatory B cells expressing IL-10 (B10 cells) requires antigen receptor diversity and TLR signals. J Immunol 2009; 182
Llorente L, Zou W, Levy Y. Role of IL 10 in the B lymphocyte hyperactivity and autoantibody production of human systemic lupus erythematosus. J Exp Med 1995; 181
Barcellini W, Rizzardi GP, Borghi MO, Nicoletti F, Fain C, Del Papa N, Meroni PL. In vitro type-1 and type-2 cytokine production in systemic lupus erythematosus: lack of relationship with clinical disease activity. Lupus 1996; 5
Ravirajan CT, Wang Y, Matis LA, Papadaki L, Griffiths MH, Latchman DS, Isenberg DA. Effect of neutralizing antibodies to IL-10 and C5 on the renal damage caused by a pathogenic human anti-dsDNA antibody. Rheumatology (Oxford) 2004; 43
Johanneson B, Lima G, von Salomé J. A major susceptibility locus for systemic lupus erythematosus maps to chromosome lq31. Am J Hum Genet 2002; 71
Khoa PD, Sugiyama T, Yokochi T. Polymorphism of interleukin-10 promoter and tumor necrosis factor receptor II in Vietnamese patients with systemic lupus erythematosus. Clin Rheumatol 2005; 24
Tan EM, Cohen AS, Fries JF, Masi AT, McShane DJ, Rothfield NF, et al.
The 1982 revised criteria for the classification of systemic lupus erythematosus. Arthritis Rheum 1982; 25
Hochberg MC. Updating the American College of Rheumatology revised criteria for the classification of systemic lupus erythematosus [letter]. Arthritis Rheum 1997; 40
Bombardier C, Gladman DD, Urowitz MB, Caron D, Chang CH. Derivation of the SLEDAI. A disease activity index for lupus patients. The Committee on Prognosis Studies in SLE. Arthritis Rheum 1992; 35
Mavrothalassitis G, Ghysdael J. Proteins of the ETS family with transcriptional repressor activity. Oncogene 2000; 19
Mok CC, Yap DY, Navarra SV, Liu ZH, Zhao MH, Lu L, et al
. Asian Lupus Nephritis Network (ALNN). Overview of lupus nephritis management guidelines and perspective from Asia. Nephrology (Carlton) 2014; 19
Tiffin N, Adeyemo A, Okpechi I. A diverse array of genetic factors contribute to the pathogenesis of systemic lupus erythematosus. Orphanet J Rare Dis 2013; 8
Tsokos GC. Mechanisms of diseases, systemic lupus erythematosus. N Engl J Med 2011; 365
Akbarian M, Faezi ST, Gharibdoost F, Shahram F, Nadji A, Jamshidi AR, et al
. Systemic lupus erythematosus in Iran: a study of 2280 patients over 33 years. Int J Rheum Dis 2010; 13
Connolly JJ, Hakonarson H. Role of cytokines in systemic lupus erythematosus: recent progress from GWAS and sequencing. J Biomed Biotechnol 2012; 2012:798924.
Liu P, Song J, Su H, Li L, Lu N, Yang R, Peng Z. IL-10 gene polymorphisms and susceptibility to systemic lupus erythematosus: a meta-analysis. PLoS One 2013; 8
Mellor-Pita S, Citores MJ, Castejon R, Yebra-Bango M, Tutor-Ureta P, Rosado S, et al
. Monocytes and T lymphocytes contribute to a predominance of interleukin 6 and interleukin 10 in systemic lupus erythematosus. Cytometry B Clin Cytom 2009; 76
Chun HY, Chung JW, Kim HA, Yun JM, Jeon JY, Ye YM, et al
. Cytokine IL-6 and IL-10 as biomarkers in systemic lupus erythematosus. J Clin Immunol 2007; 27
El-Sayed M, Nofal E, Al Mokadem S, et al.
Correlative study of serum Th1/Th2 cytokines levels in patients with systemic lupus erythematosus with SLEDAI. Egypt Dermatol Online J 2008; 4
Gross JA, Johnston J, Mudri S, Enselman R, Dillon SR, Madden K, et al
. TACI and BCMA are receptors for a TNF homologue implicated in B-cell autoimmune disease. Nature 2000; 404
Hondowicz BD, Alexander ST, Quinn WJ III, Pagán AJ, Metzgar MH, Cancro MP, Erikson J. The role of BLyS/BLyS receptors in anti-chromatin B cell regulation. Int Immunol 2007; 19
Moulin V, Andris F, Thielemans K, Maliszewski C, Urbain J, Moser M. B lymphocytes regulate dendritic cell (DC) function in vivo: increased interleukin 12 production by DCs from B cell-deficient mice results in T helper cell type 1 deviation. J Exp Med 2000; 192
Jacobi AM, Odendahl M, Reiter K, Bruns A, Burmester GR, Radbruch A, et al
. Correlation between circulating CD27 high plasma cells and disease activity in patients with systemic lupus erythematosus. Arthritis Rheum 2003; 48
Arora V, Verma J, Marwah V, Kumar A, Anand D, Das N. Cytokine imbalance in systemic lupus erythematosus: a study on northern Indian subjects. Lupus 2012; 21
Chen J, Shen B, Jiang Y, Jun L, Zhu M, Chen B, Liu C. Analysis of immunoglobulin-like transcripts (ILTs) in lymphocytes with sHLA-G and IL10 from SLE patients. Clin Exp Med 2013; 13
Dhir V, Singh AP, Aggarwal A, Naik S, Misra R. Increased T-lymphocyte apoptosis in lupus correlates with disease activity and may be responsible for reduced T-cell frequency: a cross-sectional and longitudinal study. Lupus 2009; 18
Zhou M, Ding L, Peng H, et al.
Association of the interleukin-10 gene polymorphism (−1082A/G) with systemic lupus erythematosus: a meta-analysis. Lupus 2012; 0
Hee CS, Gun SC, Naidu R, Gupta E, Somnath SD, Radhakrishnan AK. Comparison of single nucleotide polymorphisms in the human interleukin-10 gene promoter between rheumatoid arthritis patients and normal subjects in Malaysia. Mod Rheumatol 2007; 17
Mok CC, Lanchbury JS, Chan DW, Lau CS. Interleukin-10 promoter polymorphisms in Southern Chinese patients with systemic lupus erythematosus. Arthritis Rheum 1998; 41
Hee CS, Gun SC, Naidu R, Somnath SD, Radhakrishnan AK. The relationship between single nucleotide polymorphisms of the interleukin 10 gene promotor in systemic lupus erythematosus patients in Malaysia: a pilot study. Int J Rheum Dis 2008; 11
Sobkowiak A, Lianeri M, Wudarski M, £acki JK, Jagodziñski PP. Genetic variation in the interleukin 10 gene promoter in Polish patients with systemic lupus erythematosus. Rheumatol Int 2009; 29
Fei GZ, Svenungsson E, Frostegård J, Padyukov L. The A-1082 IL 10 allele is associated with cardiovascular disease in SLE. Atherosclerosis 2004; 177
Nath SK, Harley JB, Lee YH. Polymorphisms of complement receptor 1 and interleukin-10 genes and systemic lupus erythematosus: a meta-analysis. Hum Genet 2005; 118
D′Alfonso S, Giordano M, Mellai M, Lanceni M, Barizzone N, Marchini M, et al
. Association tests with systemic lupus erythematosus (SLE) of IL10 markers indicate a direct involvement of a CA repeat in the 5¢ regulatory region. Genes Immun 2002; 3
Van der Linden MW, Westendorp RG, Sturk A, Bergman W, Huizinga TW. High interleukin 10 production in first-degree relatives of patients with generalized but not cutaneous lupus erythematosus. J Investig Med 2000; 48
Lazarus M, Hajeer AH, Turner D, Sinnott P, Worthington J, Ollier WE, Hutchinson IV. Genetic variation in the interleukin 10 gene promoter and systemic lupus erythematosus. J Rheumatol 1997; 24
López P, Gutiérrez C, Suárez A. IL 10 and TNF-a genotypes in SLE. Journal of Biomedicine and Biotechnology 2010; 2010:838390.
[Table 1], [Table 2], [Table 3], [Table 4], [Table 5], [Table 6]