Yamada Ryo, Ymamoto Kazuhiko
Laboratory for Rheumatic Diseases, SNP Research Center, The Institute of Physical and Chemical Research (RIKEN), 1-7-22 Suehirocho, Tsurumi-ku, Yokohama, Kanagawa 230-0045, Japan.
Mutat Res. 2005 Jun 3;573(1-2):136-51. doi: 10.1016/j.mrfmmm.2004.06.061.
Inflammatory diseases encompass a variety of medical conditions. In this chapter, autoimmune diseases and allergic disorders will be our focus. The autoimmune diseases include organ-specific autoimmunities, such as type I diabetes mellitus and autoimmune thyroiditis (AITD), and organ non-specific disorders such as systemic lupus erythematosus (SLE). All of them seem to share aspects of aberrant immunologic tolerance toward self-antigens. Asthma and atopic diathesis are among the allergies. Crohn disease and SLE are relatively rare with a prevalence of 10-50 per 100,000, and rheumatoid arthritis (RA), psoriasis, AITD and asthma are commoner with a prevalence of 500 per 100,000 or much higher. The difference among ethnic groups is not prominent for rheumatoid arthritis, psoriasis, AITD or asthma, but Crohn disease and SLE affect some ethnic populations more than others. Although all of these disorders have some environmental component, asthma and atopy seem most affected by environmental factors, as is suggested by the significant increase in their incidence over the last several decades with changes in various environmental factors, especially in developed countries. Over the last 10 years, multiple linkage studies revealed many disease-linked loci throughout the genome with various consistencies. As implicated by some pathophysiological studies of inflammatory immune system related disorders, certain loci are involved in multiple disorders. In the following sections, reports on the identification of disease-associated genes or markers will be summarized for individual diseases (cytotoxic T lymphocyte-associated 4 (CTLA4), CARD15, DLG5, SLC22A4/A5, programmed cell death 1 (PDCD1), RUNX1, SLC9A3R1/NAT9, PADI4, ADAM33, DPP10, PHF11 and GPRA), followed by a discussion of the genes that have been implicated in multiple disorders.
炎症性疾病包括多种医学病症。在本章中,自身免疫性疾病和过敏性疾病将是我们关注的重点。自身免疫性疾病包括器官特异性自身免疫病,如1型糖尿病和自身免疫性甲状腺炎(AITD),以及器官非特异性疾病,如系统性红斑狼疮(SLE)。它们似乎都存在对自身抗原异常免疫耐受的情况。哮喘和特应性素质属于过敏症。克罗恩病和SLE相对罕见,患病率为每10万人中有10 - 50例,而类风湿关节炎(RA)、银屑病、AITD和哮喘更为常见,患病率为每10万人中有500例或更高。类风湿关节炎、银屑病、AITD或哮喘在不同种族群体中的差异不显著,但克罗恩病和SLE对某些种族人群的影响大于其他人群。尽管所有这些病症都有一定的环境因素,但哮喘和特应性似乎受环境因素影响最大,过去几十年中随着各种环境因素的变化,尤其是在发达国家,它们的发病率显著上升就表明了这一点。在过去10年中,多项连锁研究在整个基因组中发现了许多与疾病相关的位点,其一致性各不相同。正如一些炎症性免疫系统相关病症的病理生理学研究所暗示的,某些位点涉及多种病症。在以下各节中,将总结针对个别疾病(细胞毒性T淋巴细胞相关抗原4(CTLA4)、CARD15、DLG5、SLC22A4/A5、程序性细胞死亡1(PDCD1)、RUNX1、SLC9A3R1/NAT9、PADI4、ADAM33、DPP10、PHF11和GPRA)的疾病相关基因或标志物的鉴定报告,随后讨论涉及多种病症的基因。