Kristiansen O P, Larsen Z M, Pociot F
Steno Diabetes Center, Niels Steensensvej 2, DK-2820 Gentofte, Denmark.
Genes Immun. 2000 Feb;1(3):170-84. doi: 10.1038/sj.gene.6363655.
For most autoimmune disorders, the pattern of inheritance is very complex. The major histocompatibility complex (MHC) gene complex has been implicated as the major genetic component in the predisposition to these diseases but other genes are likely to be involved. Based on function and experimental data, the gene encoding cytotoxic T lymphocyte-associated antigen 4 (CTLA4) has been suggested as a candidate gene for conferring susceptibility to autoimmunity. In this review, we critically evaluate the evidence for pathogenetical involvement of CTLA-4 in the different autoimmune diseases with focus on the possible role of genetic variation of the CTLA4 locus.
对于大多数自身免疫性疾病而言,其遗传模式非常复杂。主要组织相容性复合体(MHC)基因复合体被认为是这些疾病易感性的主要遗传成分,但可能还涉及其他基因。基于功能和实验数据,编码细胞毒性T淋巴细胞相关抗原4(CTLA4)的基因已被提出作为赋予自身免疫易感性的候选基因。在本综述中,我们严格评估CTLA-4在不同自身免疫性疾病发病机制中所涉及的证据,重点关注CTLA4基因座遗传变异的可能作用。