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使用新抗原特异性单克隆抗体对类风湿性关节炎和骨关节炎患者关节组织中的补体激活进行免疫组织化学测定。

Immunohistochemical determination of complement activation in joint tissues of patients with rheumatoid arthritis and osteoarthritis using neoantigen-specific monoclonal antibodies.

作者信息

Kemp P A, Spragg J H, Brown J C, Morgan B P, Gunn C A, Taylor P W

机构信息

Research and Preclinical Development, CIBA-Geigy Pharmaceuticals, West Sussex, UK.

出版信息

J Clin Lab Immunol. 1992;37(4):147-62.

PMID:1285067
Abstract

Murine monoclonal antibodies specific for neoepitopes expressed by C9 incorporated into membrane attack complexes and by membrane-bound C3b and iC3b have been prepared and characterised. These reagents were used to determine the extent and locus of complement activation in synovial-tissues obtained from patients with rheumatoid arthritis and osteoarthritis. In the four rheumatoid arthritis patients there was extensive deposition of C3 activation products and C5b-9 complexes onto the synovial membrane and the pattern of deposition of both neoantigens in serial tissue sections was very similar. There was less extensive staining for C3 and, particularly, C9 neoepitopes on the apical surface of vessel endothelia. In two of four osteoarthritic patients a similar pattern of C3 and C9 neoepitope deposition was found; in the remaining patients no C5b-9 could be located. Synovial vessel walls, but not synovial cells, from both groups of patients stained extensively for the complement regulatory protein CD59. In synovial membranes from patients with osteoarthritis, C9 appeared to be present predominantly in SC5b-9 complexes whereas in rheumatoid arthritis patients no evidence of S-protein incorporation into membrane attack complexes could be demonstrated, suggesting that in rheumatoid arthritis there is damage to the synovial membrane as a result of complement activation and C5b-9 deposition.

摘要

已制备并表征了对整合到膜攻击复合物中的C9以及膜结合的C3b和iC3b所表达的新表位具有特异性的鼠单克隆抗体。这些试剂用于确定类风湿性关节炎和骨关节炎患者滑膜组织中补体激活的程度和部位。在四名类风湿性关节炎患者中,C3激活产物和C5b - 9复合物广泛沉积在滑膜上,并且在连续组织切片中两种新抗原的沉积模式非常相似。血管内皮细胞顶端表面的C3,尤其是C9新表位的染色范围较小。在四名骨关节炎患者中的两名中,发现了类似的C3和C9新表位沉积模式;在其余患者中未发现C5b - 9。两组患者的滑膜血管壁而非滑膜细胞对补体调节蛋白CD59进行了广泛染色。在骨关节炎患者的滑膜中,C9似乎主要存在于SC5b - 9复合物中,而在类风湿性关节炎患者中,没有证据表明S蛋白整合到膜攻击复合物中,这表明在类风湿性关节炎中,补体激活和C5b - 9沉积导致滑膜损伤。

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