Chaplin D D, Kemp M E
Howard Hughes Medical Institute, Washington University School of Medicine, St. Louis, Mo.
Year Immunol. 1988;3:179-98.
Study of two diseases with autoimmune characteristics (IDDM and SLE) has demonstrated that alleles carried in the MHC can confer disease susceptibility. The MHC alleles most strongly associated with the development of IDDM are encoded within the class II region (HLA-DR or -DQ). Recent studies indicating that the class III gene products TNF alpha and beta may play a critical role in the initiation of the autoimmune attack on the pancreatic beta-cells have suggested the possibility that the class III region may also contribute to genetic susceptibility in IDDM. In SLE, although there is some evidence suggesting that certain alleles of class II genes may confer disease risk, a more striking association has been detected in the class III region. Deficiency of the class III encoded C4A molecule (either homozygously or heterozygously) shows a high correlation with disease risk. This finding is attractive because C4A plays a central role in the metabolism of immune complexes, the aberrant deposition of which leads to the most prominent alterations in SLE.
对两种具有自身免疫特征的疾病(胰岛素依赖型糖尿病和系统性红斑狼疮)的研究表明,主要组织相容性复合体(MHC)中携带的等位基因可赋予疾病易感性。与胰岛素依赖型糖尿病发病最密切相关的MHC等位基因在Ⅱ类区域(HLA - DR或 - DQ)内编码。最近的研究表明,Ⅲ类基因产物肿瘤坏死因子α和β可能在针对胰腺β细胞的自身免疫攻击的启动中起关键作用,这提示Ⅲ类区域也可能对胰岛素依赖型糖尿病的遗传易感性有影响。在系统性红斑狼疮中,虽然有一些证据表明Ⅱ类基因的某些等位基因可能赋予疾病风险,但在Ⅲ类区域检测到了更显著的关联。Ⅲ类编码的C4A分子缺陷(纯合或杂合)与疾病风险高度相关。这一发现很有吸引力,因为C4A在免疫复合物的代谢中起核心作用,免疫复合物的异常沉积会导致系统性红斑狼疮中最显著的病变。