Multiplex family–based study in systemic lupus erythematosus: association between the R620W polymorphism of PTPN22 and the FcγRIIa (CD32A) R131 allele

Abstract

A functional polymorphism in PTPN22, a gene encoding a phosphatase involved in T-cell signaling, has been associated with autoimmunity. We checked for the prevalence of the PTPN22 R620W polymorphism in multiplex families affected with systemic lupus erythematosus (SLE) and other autoimmune diseases. Its association with other polymorphisms in mannose binding lectin (MBL) and FcgammaRIIa (CD32A) genes was also studied. Deoxyribonucleic acid samples were obtained from 233 Spanish individuals who belonged to 21 families in which at least two members had been diagnosed with some autoimmune disease, mainly SLE. A healthy control population was also included (n= 129). Genotyping for the R620W single-nucleotide polymorphism (SNP) was performed by restriction fragment length polymorphism analysis of polymerase chain reaction products. Allele frequency for the T allele was slightly higher in the families with autoimmune disease, especially when considering the affected individuals (0.094 vs 0.062). Actually, 18.8% affected family members vs 11.6% controls had the polymorphism (P= 0.179). Nineteen percent of affected individuals had both the PTPN22 T and the CD32A R131 alleles, whereas only 8.5% unaffected relatives had both susceptibility alleles simultaneously [P= 0.031, odds ratios 2.508 (95% confidence interval 1.066-5.896)]. The tendency toward finding the T allele more frequently in members affected with some particular autoimmune disorder suggests that this SNP may confer susceptibility to autoimmunity. The fact that more affected than unaffected relatives carried both the T and the R131 alleles simultaneously leads us to think about the existence of a combinatorial effect between genes that could help define individuals prone to autoimmune diseases.

Association of an NKG2D gene variant with systemic lupus erythematosus in two populations

“…Twin and family studies have revealed a genetic contribution to the etiology of the disease. Meanwhile, a number of risk genes, including BLK, Bank-1, TNFSF4, IRF-5, STAT-4, PTPN22, PD-1, CD11b, and CD32A have been identified [1][2][3][4][5][6][7][8][9][10]. In addition, chronic viral infections may induce the disease and participate in its pathogenesis.…”

PTPN22 1858T is not a risk factor for North American Pemphigus vulgaris

“…The PTPN22 1858T allele has been positively associated with a number of humoral autoimmune diseases including rheumatoid arthritis (12,17), type 1 diabetes (18,19), and systemic lupus erythematosus (20). The presence of a single PTPN22 1858T allele (1858C/1858T, herein referred to as the 1858C/T genotype) is sufficient to confer risk to disease (12,14,17–20). The homozygous 1858T/1858T (1858T/T) genotype is rare, but confers an additional disease risk (16).…”

“…This increase in immune system function has been postulated to play a role in the eventual progression to autoimmunity (15,16). The PTPN22 1858T allele has been positively associated with a number of humoral autoimmune diseases including rheumatoid arthritis (12,17), type 1 diabetes (18,19), and systemic lupus erythematosus (20). The presence of a single PTPN22 1858T allele (1858C ⁄ 1858T, herein referred to as the 1858C ⁄ T genotype) is sufficient to confer risk to disease (12,14,(17)(18)(19)(20).…”

The PTPN22*R620W polymorphism does not confer genetic susceptibility to antiphospholipid syndrome in the Spanish population

“…Genomic DNA was isolated from peripheral blood leucocytes by standard methods. Genotyping of PTPN22*R620W was carried‐out by polymerase chain reaction–restricted fragment length polymorphism assay as previously described (Balada et al. , 2006).…”