Association of MICA-129Met/Val polymorphism with clinical outcome of anti-TNF therapy and MICA serum levels in patients with rheumatoid arthritis

被引:17
|
作者
Iwaszko, Milena [1 ]
Swierkot, Jerzy [2 ]
Dratwa, Marta [1 ]
Wysoczanska, Barbara [1 ]
Korman, Lucyna [2 ]
Bugaj, Bartosz [2 ]
Kolossa, Katarzyna [3 ]
Jeka, Slawomir [3 ]
Wiland, Piotr [2 ]
Bogunia-Kubik, Katarzyna [1 ]
机构
[1] Polish Acad Sci, Hirszfeld Inst Immunol & Expt Therapy, Lab Clin Immunogenet & Pharmacogenet, Wroclaw, Poland
[2] Wroclaw Med Univ, Dept Rheumatol & Internal Med, Wroclaw, Poland
[3] Jan Biziel Univ Hosp 2, Dept Rheumatol & Connect Tissue Dis, Collegium Medicum Bydgoszcz, UMK, Torun, Poland
来源
PHARMACOGENOMICS JOURNAL | 2020年 / 20卷 / 06期
关键词
MAJOR HISTOCOMPATIBILITY COMPLEX; CD4(+)CD28(-) T-CELLS; NKG2D RECEPTOR; EXPRESSION; LIGANDS; ACTIVATION; DIMORPHISM; GENE; SUSCEPTIBILITY; RESPONSES;
D O I
10.1038/s41397-020-0164-3
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
MHC class I polypeptide-related sequence A (MICA) is a stress-induced protein involved in activation of NK and T cells through interaction with NKG2D receptor. These molecules are atypically expressed in synovium of patients diagnosed with rheumatoid arthritis (RA). A total of 279 patients with RA, qualified to TNF-blockade therapy, were genotyped for MICA rs1051792 SNP. The effectiveness of anti-TNF agents was assessed with European League Against Rheumatism criteria. Significant relationship between MICA rs1051792 and outcome of TNF-blockade therapy has been found. The MICA rs1051792 GG genotype was overrepresented in patients non-responsive to anti-TNF drugs in comparison with other genotypes (p = 0.010). On the other hand, beneficial therapeutic response was more frequently detected among RA subjects possessing heterozygous genotype than those with homozygous genotypes (p = 0.003). Furthermore, increased MICA concentrations in serum were observed in patients possessing MICA rs1051792 GG genotype as compared with those with GA or AA genotypes (p = 1.8 x 10(-5)). The results from this study indicate the potential influence of MICA rs1051792 polymorphism on modulation of therapeutic response to TNF-blockade treatment in RA.
引用
收藏
页码:760 / 769
页数:10
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