de Rooij D J, van de Putte L B, Habets W J, Verbeek A L, van Venrooij W J
Department of Rheumatology, St. Maartenskliniek, Nijmegen, The Netherlands.
Scand J Rheumatol. 1988;17(5):353-64. doi: 10.3109/03009748809105271.
Using the immunoblotting technique, sera from 433 patients with rheumatic diseases were screened for the presence of antibodies against several nuclear and cytoplasmic antigens, such as RNP, Sm, Ro(SSA), La(SSB), CR-19 (centromeric antigen), Topo-1 (Scl-70), Jo-1, histone and 56 kD. At the same time clinical data from these patients were collected without prior knowledge of the immunoblotting results. Syndrome-specific autoantibodies were found for mixed connective tissue disease (antibodies against the RNP related 70 kD antigen), for CREST (anti-CR-19 antibodies), for diffuse scleroderma (anti-Topo-1 antibodies) and for polymyositis (anti-Jo-1 antibodies). Almost all specific autoantibodies were present exclusively in patients with a connective tissue disease. Controls were only in a few cases positive for antihistone and anti-56 kD antibodies. Associations of specific autoantibodies with clinical and laboratory features of the patients were mostly as expected. However, some unexpected associations were found, for example polymyositis and calcinosis with anti-Sm antibodies, sicca symptoms with anti-centromere antibodies and leucopenia with Ro(SSA) and La(SSB).
采用免疫印迹技术,对433例风湿性疾病患者的血清进行检测,以筛查针对多种核抗原和胞质抗原的抗体,如核糖核蛋白(RNP)、史密斯(Sm)、Ro(SSA)、La(SSB)、着丝粒抗原(CR-19)、拓扑异构酶-1(Scl-70)、Jo-1、组蛋白和56kD。同时,在不了解免疫印迹结果的情况下收集这些患者的临床资料。发现混合性结缔组织病(抗RNP相关70kD抗原抗体)、CREST综合征(抗CR-19抗体)、弥漫性硬皮病(抗拓扑异构酶-1抗体)和多发性肌炎(抗Jo-1抗体)存在综合征特异性自身抗体。几乎所有特异性自身抗体仅存在于结缔组织病患者中。对照组仅少数病例抗组蛋白和抗56kD抗体呈阳性。特异性自身抗体与患者临床及实验室特征的关联大多与预期相符。然而,也发现了一些意外的关联,例如多发性肌炎和钙质沉着与抗Sm抗体、干燥症状与抗着丝粒抗体、白细胞减少与Ro(SSA)和La(SSB)。