Veys E M, Hermanns P, Goldstein G, Kung P, Schindler J, Van Wauwe J
Int J Immunopharmacol. 1981;3(3):313-9. doi: 10.1016/0192-0561(81)90025-4.
The pathogenesis of rheumatoid arthritis is unknown, but clear abnormalities of the immune system are well documented in this disease. We therefore evaluated T cell subpopulations in patients with rheumatoid arthritis using monoclonal antibodies previously shown to react with all T cells (OKT3), with inducer/helper T cells (OKT4) and with suppressor/cytotoxic T cells (OKT8). These investigations disclosed evidence of a significant decrease in the number of OKT8+ cells/mm3 and a high inducer-helper/suppressor-cytotoxic (OKT4+/OKT8+) ratio in active rheumatoid arthritis. A modest number of patients with active arthritis were treated wit levamisole or with synthetic thymopoietin 32-36 (thymopoietin pentapeptide or TP-5). These individuals responded with ratio decreases to more normal levels. Our data support the hypothesis that monoclonal T cell antibodies may offer an important tool for the further evaluation of patients with rheumatoid arthritis and their individual response to treatment.
类风湿性关节炎的发病机制尚不清楚,但该疾病中免疫系统明显异常已有充分记录。因此,我们使用先前已证明能与所有T细胞(OKT3)、诱导/辅助性T细胞(OKT4)以及抑制/细胞毒性T细胞(OKT8)发生反应的单克隆抗体,对类风湿性关节炎患者的T细胞亚群进行了评估。这些研究揭示,在活动性类风湿性关节炎中,每立方毫米OKT8+细胞数量显著减少,且诱导/辅助性/抑制/细胞毒性(OKT4+/OKT8+)比值较高。少数活动性关节炎患者接受了左旋咪唑或合成胸腺生成素32 - 36(胸腺生成素五肽或TP - 5)治疗。这些个体的比值下降至更正常的水平。我们的数据支持这样一种假说,即单克隆T细胞抗体可能为进一步评估类风湿性关节炎患者及其对治疗的个体反应提供重要工具。