中国强直性脊柱炎人群的免疫遗传学研究:最近发现了特异性基因吗?

Clinical & Developmental Immunology Pub Date : 2013-01-01 Epub Date: 2013-01-16 DOI:10.1155/2013/419357
Jiayu Zhai, Ju Rong, Qiuxia Li, Jieruo Gu
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引用次数: 18

摘要

目的:强直性脊柱炎(AS)是一种导致受影响关节破坏的系统性自身免疫性疾病。在过去的5年中,在中国人群中发现了几个与AS相关的新基因或遗传区域。本文旨在讨论这些研究在我国人群中的主要发现和相关的潜在机制。近年来,由于计算遗传学和技术的快速发展,越来越多的基因或遗传区域与AS易感性相关。到目前为止,在中国汉族人群中已经报道了几个基因或遗传区域,包括主要组织相容性复合体(MHC)、ERAP1、IL-23R、12q12、2p15、5q14.3等。在对这些基因或遗传区域功能研究的基础上,对疾病机制进行了不同的假设。摘要:本文试图总结几个候选基因与中国汉族AS风险的关联,旨在识别新的炎症途径,并为更好的治疗提供潜在的策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Immunogenetic study in Chinese population with ankylosing spondylitis: are there specific genes recently disclosed?

Purpose: Ankylosing spondylitis (AS) is a systemic, autoimmune disease resulting in the destruction of the affected joints. Over the past 5 years, several new genes or genetic regions associated with AS have been identified in the Chinese population. This paper aims to discuss the major findings and related potential mechanisms of these studies in our population.

Recent findings: In recent years, due to the rapid advances in computational genetics and technology, there has been an increasing list of well-validated genes or genetic regions associated with AS susceptibility. So far, several genes or genetic regions have now been reported in the Han ethnic Chinese population, containing the major histocompatibility complex (MHC), ERAP1, IL-23R, 12q12, 2p15, 5q14.3, and so on. Different hypotheses for disease mechanisms have been investigated on the basis of the functional studies of these genes or genetic regions.

Summary: This paper tries to summarize the association of several candidate genes with risk for AS in the Han ethnic Chinese population and aims to identify the novel inflammatory pathways and provide potential strategies for better therapies.

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