Krause A, Goebel K M
Department of Medicine, University Hospital, Marburg, West Germany.
J Clin Lab Immunol. 1987 Sep;24(1):25-7.
Recent studies indicate that the susceptibility to various inflammatory rheumatic diseases is an inherited trait determined by gene products of the class II histocompatibility complex (HLA-DR determinants). In a study designed to evaluate the concept of inherited susceptibility to sarcoid arthritis (SA), 42 patients with histologically proved acute disease underwent typing of HLA-A, -B, -C and -DR antigens. Using the microdroplet assay of human serum cytotoxins, we employed 156 antiserums to identify 52 antigens on A, B and C loci and 35 to identify 7 DR antigens on the surface of B cells. An ethnically matched control group consisted of 134 healthy volunteers. The frequency of B cell isoantigen DR3 specificity was significantly increased in patients with SA (relative risk, 4.8); HLA-DR3 was found in 25 (60%) of the patients, compared with 31 (23%) of the controls. This study lends further support to the hypothesis that the putative role of an infectious agent triggering SA cannot be judged without considering genetic cofactors.
近期研究表明,对各种炎性风湿性疾病的易感性是一种由Ⅱ类组织相容性复合体(HLA - DR决定簇)的基因产物所决定的遗传性状。在一项旨在评估结节病关节炎(SA)遗传易感性概念的研究中,42例经组织学证实为急性疾病的患者接受了HLA - A、- B、- C和 - DR抗原分型。我们使用人血清细胞毒素的微滴分析法,用156种抗血清鉴定A、B和C位点上的52种抗原,并用35种抗血清鉴定B细胞表面的7种DR抗原。一个种族匹配的对照组由134名健康志愿者组成。SA患者中B细胞同种抗原DR3特异性的频率显著增加(相对风险,4.8);25例(60%)患者中发现有HLA - DR3,而对照组中为31例(23%)。这项研究进一步支持了这样一种假说,即如果不考虑遗传辅助因素,就无法判断触发SA的感染因子的假定作用。