Life P, Hassell A, Williams K, Young S, Bacon P, Southwood T, Gaston J S
Department of Rheumatology, Birmingham University, UK.
J Rheumatol. 1993 Aug;20(8):1388-96.
To investigate the antigenic specificity of synovial T cells in juvenile chronic arthritis (JCA).
Synovial fluid and peripheral blood mononuclear cells from 24 patients with JCA were tested for their proliferative responses to recall antigens, enteric organisms associated with reactive arthritis, influenza A and a recombinant preparation of a mycobacterial heat shock protein, HSP65. To investigate further recognition of this last antigen, synovial T cells from one B27+ patient with pauciarticular disease were cloned using HSP65. The specificity of the resultant clones was then examined.
Marked synovial T cell responses to enteric organisms and to HSP65 were noted, particularly in HLA-B27+, pauciarticular patients; these were similar to those seen in a B27+ patient with reactive arthritis. Responses to enteric organisms and to HSP65 were significantly correlated, suggesting recognition of an epitope common to these antigen preparations. However, all of the T cell clones obtained using HSP65 proved to recognize E. coli derived antigens contaminating the recombinant HSP65 rather than the mycobacterial antigen; these contaminants included the 60 kDa E. coli HSP, GroEL. The GroEL specific T cells did not respond to heat shocked human cells; this suggests (but does not prove) that they do not crossreact with human HSP60.
Synovial T cell recognition of antigens from enteric organisms associated with reactive arthritis is a common feature in pauciarticular JCA. Among the target antigens is the GroEL HSP, but T cells recognizing this antigen do not necessarily crossreact with the homologous human HSP60.
研究青少年慢性关节炎(JCA)中滑膜T细胞的抗原特异性。
检测24例JCA患者的滑液和外周血单个核细胞对回忆抗原、与反应性关节炎相关的肠道微生物、甲型流感病毒以及一种分枝杆菌热休克蛋白HSP65重组制剂的增殖反应。为进一步研究对最后一种抗原的识别情况,利用HSP65对1例B27阳性少关节病患者的滑膜T细胞进行克隆,然后检测所得克隆的特异性。
观察到滑膜T细胞对肠道微生物和HSP65有明显反应,特别是在HLA - B27阳性少关节病患者中;这些反应与1例反应性关节炎B27阳性患者的反应相似。对肠道微生物和HSP65的反应显著相关,提示识别这些抗原制剂共有的一个表位。然而,所有利用HSP65获得的T细胞克隆均被证明识别污染重组HSP65的大肠杆菌衍生抗原,而非分枝杆菌抗原;这些污染物包括60 kDa大肠杆菌HSP,即GroEL。GroEL特异性T细胞对热休克人细胞无反应;这提示(但未证实)它们不会与人HSP60发生交叉反应。
滑膜T细胞对与反应性关节炎相关的肠道微生物抗原的识别是少关节型JCA的一个常见特征。靶抗原中包括GroEL HSP,但识别该抗原的T细胞不一定与人同源HSP60发生交叉反应。