Arnett F C, Hirsch T J, Bias W B, Nishikai M, Reichlin M
J Rheumatol. 1981 Nov-Dec;8(6):925-30.
Antibodies to Jo-1, a saline extractable nuclear antigen, were found in 11/47 (23%) patients with myositis and in 0/35 controls with systemic lupus erythematosus or progressive systemic sclerosis (p less than or equal to 0.01). Within myositis subgroups, anti-Jo-1 occurred in 6/20 (30%) with polymyositis, 2/16 (13%) with dermatomyositis and 3/7 (43%) with overlap. There was an association between Jo-1 antibodies and HLA-DR3, irrespective of race or clinical subgroups (p less than or equal to 0.05). All anti-Jo-1 positive patients had either HLA-DR3, HLA-DRW6 or both (p less than or equal to 0.01). Thus, this antibody system might arise as a result of an aberrant immune response mediated at or near HLA-D in patients with myositis.
在47例肌炎患者中,有11例(23%)检测到针对可盐提取核抗原Jo-1的抗体,而在35例系统性红斑狼疮或进行性系统性硬化症对照患者中未检测到(p≤0.01)。在肌炎亚组中,抗Jo-1抗体出现在20例多发性肌炎患者的6例(30%)、16例皮肌炎患者的2例(13%)以及7例重叠综合征患者的3例(43%)中。无论种族或临床亚组如何,Jo-1抗体与HLA-DR3之间均存在关联(p≤0.05)。所有抗Jo-1阳性患者均具有HLA-DR3、HLA-DRW6或两者兼具(p≤0.01)。因此,该抗体系统可能是肌炎患者中在HLA-D处或其附近介导的异常免疫反应的结果。