Korman Benjamin D, Kastner Daniel L, Gregersen Peter K, Remmers Elaine F
National Institute of Arthritis, Musculoskeletal, and Skin Diseases, 9 Memorial Drive, NIH Building 9, Room 1W108, Bethesda, MD 20892, USA.
Curr Allergy Asthma Rep. 2008 Sep;8(5):398-403. doi: 10.1007/s11882-008-0077-8.
Recent advances in genetics and technology have led to breakthroughs in understanding the genes that predispose individuals to autoimmune diseases. A common haplotype of the signal transducer and activator of transcription 4 (STAT4) gene has been shown to be associated with susceptibility to rheumatoid arthritis, systemic lupus erythematosus, and primary Sjögren's syndrome. STAT4 is a transcription factor that transduces interleukin-12, interleukin-23, and type 1 interferon cytokine signals in T cells and monocytes, leading to T-helper type 1 and T-helper type 17 differentiation, monocyte activation, and interferon-gamma production. Although the evidence for this association is very strong and well replicated, the exact mechanism by which polymorphisms in this gene lead to disease remains unknown. In concert with the identification of other disease-associated loci, elucidating how the variant form of STAT4 modulates immune function should lead to an improved understanding of the pathophysiology of autoimmunity.
遗传学和技术方面的最新进展已在理解使个体易患自身免疫性疾病的基因方面取得突破。转录信号转导子与激活子4(STAT4)基因的一种常见单倍型已被证明与类风湿性关节炎、系统性红斑狼疮和原发性干燥综合征的易感性相关。STAT4是一种转录因子,可在T细胞和单核细胞中转导白细胞介素-12、白细胞介素-23和1型干扰素细胞因子信号,导致1型辅助性T细胞和17型辅助性T细胞分化、单核细胞活化以及γ干扰素产生。尽管这种关联的证据非常确凿且得到了充分验证,但该基因多态性导致疾病的确切机制仍不清楚。与其他疾病相关基因座的鉴定相结合,阐明STAT4的变异形式如何调节免疫功能应有助于更好地理解自身免疫的病理生理学。