Herrmann D, Schlenvoigt G, Jäger L
Department of Clinical Immunology, Friedrich Schiller University, Jena.
Allerg Immunol (Leipz). 1987;33(2):101-9.
A solid-phase radioimmunoassay and an enzyme-linked immunosorbent assay have been developed for the identification of IgE rheumatoid factor (IgE RF). For both, human IgG was used as antigen. Bound IgE RF was detected by means of commercially available rabbit anti-human IgE antiserum and 125I-labelled sheep anti-rabbit IgG as well as monoclonal anti-human-epsilon-chain antibody and horse-radish peroxidase-labelled sheep anti-mouse IgG. The presence of IgM RF did not cause false positive results. Correlation in the results of both assays were significant, the reproducibility was very good. In 50.6% of 79 sera from patients with rheumatoid arthritis IgE RF has been detected with both or one of the methods. Only in 1 out of 12 seronegative rheumatoid arthritis sera IgE RF was identified.
已开发出一种固相放射免疫测定法和一种酶联免疫吸附测定法用于鉴定IgE类风湿因子(IgE RF)。两种方法均使用人IgG作为抗原。通过市售的兔抗人IgE抗血清和125I标记的羊抗兔IgG以及单克隆抗人ε链抗体和辣根过氧化物酶标记的羊抗鼠IgG来检测结合的IgE RF。IgM RF的存在不会导致假阳性结果。两种测定法的结果相关性显著,重现性非常好。在79例类风湿性关节炎患者的血清中,50.6%的血清通过两种方法或其中一种方法检测到了IgE RF。在12例血清阴性的类风湿性关节炎血清中,仅1例鉴定出了IgE RF。