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解析复杂疾病的遗传学:类风湿关节炎和银屑病的易感基因。

Unraveling the genetics of complex diseases: susceptibility genes for rheumatoid arthritis and psoriasis.

机构信息

Celera, 1401 Harbor Bay Parkway, Alameda, CA 94502, USA.

出版信息

Semin Immunol. 2009 Dec;21(6):318-27. doi: 10.1016/j.smim.2009.04.002. Epub 2009 May 14.

Abstract

Talk of numerous genetic risk factors for rheumatoid arthritis (RA) and psoriasis has been percolating for years, but with the exception of the human leukocyte antigen (HLA) region, none have been definitively identified. Recently the results of multiple, well powered, genetic case-control studies have begun to appear providing convincing statistical evidence for at least ten non-HLA related risk genes or loci (C5/TRAF1, CD40, CTLA4, KIF5A/PIP4K2C, MMEL1/TNFRSF14, PADI4, PRKCQ, PTPN22, STAT4, and TNFAIP3/OLIG3) for RA and six (IL12B, IL13, IL23R, STAT2/IL23A, TNFAIP3, and TNIP1) for psoriasis. These initial, novel findings are beginning to shed light on the molecular pathways pertinent to the individual diseases and highlight the pleiotropic effects of several risk factors as well as the allelic heterogeneity underlying susceptibility to these and other autoimmune diseases.

摘要

多年来,人们一直在讨论类风湿关节炎(RA)和银屑病的许多遗传风险因素,但除了人类白细胞抗原(HLA)区域外,没有一个因素得到明确确定。最近,多项强大的遗传病例对照研究的结果开始出现,为至少十个非 HLA 相关的风险基因或位点(C5/TRAF1、CD40、CTLA4、KIF5A/PIP4K2C、MMEL1/TNFRSF14、PADI4、PRKCQ、PTPN22、STAT4 和 TNFAIP3/OLIG3)提供了 RA 的令人信服的统计证据,为银屑病提供了六个(IL12B、IL13、IL23R、STAT2/IL23A、TNFAIP3 和 TNIP1)。这些最初的新发现开始揭示与这些疾病相关的分子途径,并强调了几个风险因素的多效性效应,以及这些和其他自身免疫性疾病易感性的等位基因异质性。

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