Hayman M W, van Beijnen M T A, Stamp L K, Spellerberg M B, O'Donnell J L
Immunology Section, Canterbury Health Laboratories, Christchurch, New Zealand.
J Immunol Methods. 2006 Aug 31;315(1-2):19-26. doi: 10.1016/j.jim.2006.06.013. Epub 2006 Jul 20.
Early stage rheumatoid arthritis (RA) is often difficult to diagnose because initial symptoms are non-specific. To aid diagnosis, suitable serological diagnostic markers are sought. Elevated levels of soluble MHC class II (soluble human leukocyte antigen; sHLA-DR) in human serum have been associated with rheumatoid and 'rheumatoid-like' autoimmune diseases. As a result, sHLA-DR has been suggested as a specific marker of RA. However, reported levels of sHLA-DR in sera of healthy donors vary significantly and the mechanism of release of HLA-DR into serum is poorly understood. Investigations into the diagnostic potential of this molecule necessitate the development of a sensitive and specific sHLA-DR assay. We have investigated multiple ELISA setups to develop such an assay and false positive signal has been carefully removed using a combination of isotype-matched controls and immuno-depletion. sHLA-DR levels in sera of RA patients were not significantly different from those in healthy donors which suggests sHLA-DR has limited utility in the diagnosis of RA. In RA patients, we detected high levels of sHLA-DR in aspirated synovial fluid (SF), but this did not correlate with sHLA-DR levels in serum.
早期类风湿性关节炎(RA)往往难以诊断,因为其初始症状不具有特异性。为了辅助诊断,人们一直在寻找合适的血清学诊断标志物。人血清中可溶性MHC II类分子(可溶性人类白细胞抗原;sHLA-DR)水平升高与类风湿性及“类风湿样”自身免疫性疾病有关。因此,sHLA-DR被认为是RA的一种特异性标志物。然而,健康供体血清中报道的sHLA-DR水平差异很大,且HLA-DR释放到血清中的机制尚不清楚。对该分子诊断潜力的研究需要开发一种灵敏且特异的sHLA-DR检测方法。我们研究了多种酶联免疫吸附测定(ELISA)设置来开发这样一种检测方法,并使用同型匹配对照和免疫去除相结合的方法仔细去除了假阳性信号。RA患者血清中的sHLA-DR水平与健康供体的水平没有显著差异,这表明sHLA-DR在RA诊断中的效用有限。在RA患者中,我们在抽取的滑液(SF)中检测到高水平的sHLA-DR,但这与血清中的sHLA-DR水平无关。