Fritzler M, Ryan P, Kinsella T D
J Rheumatol. 1982 Jan-Feb;9(1):46-51.
The presenting features of 25 systemic lupus erythematosus (SLE) patients with antihistone antibodies were compared to 25 age and sex matched patients who had antibodies to Sm, ribonuclear protein, Sjögren's syndrome antigen B and native DNA. The SLE patients with antihistone antibodies had a significantly lower frequency of renal disease, central nervous system disease, alopecia, anemia and hypocomplementemia. Nine of 25 (36%) age and sex matched RA patients had antihistone antibodies but in lower titers than the SLE patients. There was no correlation of antihistone antibody titers with disease activity, corticosteroid therapy or rheumatoid factor titer. Histone-antihistone complexes did not bind complement components of either the classical or alternative pathway of complement.
将25例有抗组蛋白抗体的系统性红斑狼疮(SLE)患者的临床表现与25例年龄和性别相匹配、有抗Sm、核糖核蛋白、干燥综合征抗原B和天然DNA抗体的患者进行比较。有抗组蛋白抗体的SLE患者患肾脏疾病、中枢神经系统疾病、脱发、贫血和补体低下的频率显著较低。25例年龄和性别相匹配的类风湿关节炎(RA)患者中有9例(36%)有抗组蛋白抗体,但滴度低于SLE患者。抗组蛋白抗体滴度与疾病活动度、皮质类固醇治疗或类风湿因子滴度无相关性。组蛋白-抗组蛋白复合物不结合补体经典途径或替代途径的补体成分。