Association between PDCD1 Gene Polymorphisms and Risk of Systemic Lupus Erythematosus in Three Main Ethnic Groups of the Malaysian Population

被引:21
|
作者
Chua, Kek Heng [1 ]
Lian, Lay Hoong [1 ]
Sim, Xiu Jia [1 ]
Cheah, Tien Eang [2 ]
Lau, Tze Pheng [1 ,3 ]
机构
[1] Univ Malaya, Dept Biomed Sci, Fac Med, Kuala Lumpur 50603, Malaysia
[2] Univ Malaya, Div Rheumatol, Dept Med, Fac Med, Kuala Lumpur 50603, Malaysia
[3] Univ Malaya, Dept Pathol, Fac Med, Kuala Lumpur 50603, Malaysia
关键词
PD-1; SLE susceptibility; Malaysia; SINGLE NUCLEOTIDE POLYMORPHISMS; REGULATORY POLYMORPHISM; T-CELLS; SUSCEPTIBILITY; PD-1; FREQUENCY; MANIFESTATIONS; EXPRESSION; MUTATIONS; RECEPTOR;
D O I
10.3390/ijms16059794
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The programmed cell death 1 (PDCD1) gene encodes for the PD-1 (programmed death 1) molecule, which negatively regulates self-reactive T- and B-cells in the maintenance of peripheral tolerance. A previous report had shown the development of lupus-like phenotypes in PD-1-deficient C57BL/6 mice, was suggestive to the role of PDCD1 in predisposing to systemic lupus erythematosus (SLE). Hence, we aimed to investigate the association between PDCD1 and SLE susceptibility in the Malaysian population. A TaqMan-based real-time PCR was employed to screen for PD1.1, PD1.3, PD1.5 and PD1.6 in both SLE and healthy control groups of 200 samples each. The observed frequency for PD1.5C/C genotype was significantly higher in Indian SLE patients and Malay controls (p < 0.01). On the other hand, the PD1.5C/T genotype might predispose the Malays to SLE, but confer a protective effect among the Indians (p < 0.01). The PD1.1, PD1.3 and PD1.6 were, however, not correlated to genetic predisposition of SLE in our Malaysian population. In conclusion, PD1.5 variant was significantly associated to SLE susceptibility in our Malaysian cohort. Our failure in replicating the association between other investigated PDCD1 variants and risk of getting SLE might due to ethnic and geographic variations in the distribution of these genetic variants.
引用
收藏
页码:9794 / 9803
页数:10
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