Wilder R L, Allen J B, Hansen C
J Clin Invest. 1987 Apr;79(4):1160-71. doi: 10.1172/JCI112933.
Euthymic LEW rats, when injected with streptococcal cell walls, exhibited rapid onset development of acute exudative arthritis coincident with enhanced synovial expression of Ia antigen. By 21 d after injection, the expression of Ia was markedly increased compared with basal conditions and paralleled the severity of the later developing proliferative and erosive disease. Immunodeficient athymic and cyclosporin A-treated LEW rats developed only the early phase arthritis, which was again paralleled by synovial Ia expression. Chronic expression of high levels of Ia antigen was not observed. Histocompatible F344 rats, both athymic and euthymic, developed minimal, if any, clinically significant arthritis and did not exhibit the enhanced Ia expression demonstrated in the LEW rats. Our results indicate that enhanced synovial Ia expression parallels clinical disease severity and varies by rat strain, and that the rapid onset enhanced synovial Ia expression is thymus independent, whereas the markedly enhanced chronic phase Ia expression is thymus dependent.
情绪正常的LEW大鼠注射链球菌细胞壁后,会迅速出现急性渗出性关节炎,同时滑膜Ia抗原表达增强。注射后21天,与基础状态相比,Ia的表达显著增加,且与后期发展的增殖性和侵蚀性疾病的严重程度平行。免疫缺陷的无胸腺和环孢素A处理的LEW大鼠仅发展为早期关节炎,这同样与滑膜Ia表达平行。未观察到Ia抗原的慢性高水平表达。组织相容性的F344大鼠,无论是无胸腺还是情绪正常的,都只发展出极少的(如果有的话)具有临床意义的关节炎,并且没有表现出LEW大鼠中所显示的Ia表达增强。我们的结果表明,滑膜Ia表达增强与临床疾病严重程度平行,且因大鼠品系而异,快速出现的滑膜Ia表达增强不依赖胸腺,而明显增强的慢性期Ia表达依赖胸腺。