Nordling C, Holmdahl R, Klareskog L
Department of Medical and Physiological Chemistry, Biomedical Center, Uppsala University, Sweden.
Immunology. 1991 Apr;72(4):486-90.
Monoclonal anti-idiotypic antibodies previously shown to react with a cross-reactive idiotope of anti-collagen II auto-antibodies were used for in vivo treatment of DBA/1 mice receiving immunization with arthritogenic native rat collagen type II. Injection of 100 micrograms of the anti-idiotypic antibody 3 weeks before the collagen immunization resulted in a significant suppression of collagen arthritis, compared with mice treated with a monoclonal control antibody. The treatment with anti-idiotypic antibody 3 weeks before collagen immunization could also cause a marked down-regulation of the total serum levels of anti-collagen II antibodies. When the anti-idiotypic antibodies were administered near the time for induction of arthritis (2 days after collagen immunization) a significant effect was seen on the collagen arthritis, but not on the levels of anti-collagen antibody. As collagen-induced arthritis is a disease where both T- and B-cell mediated immunity are believed to play critical roles, the present effects of the in vivo anti-idiotype treatment on arthritis development could provide an interesting system for the study of idiotype regulation on both B- and T-cell arthritis-associated autoimmunity.
先前已证明与抗胶原蛋白II自身抗体的交叉反应性独特型表位发生反应的单克隆抗独特型抗体,被用于对接受致关节炎性天然大鼠II型胶原蛋白免疫的DBA/1小鼠进行体内治疗。与用单克隆对照抗体治疗的小鼠相比,在胶原蛋白免疫前3周注射100微克抗独特型抗体可显著抑制胶原蛋白性关节炎。在胶原蛋白免疫前3周用抗独特型抗体进行治疗,也可导致抗胶原蛋白II抗体的总血清水平显著下调。当在诱导关节炎的时间附近(胶原蛋白免疫后2天)给予抗独特型抗体时,对胶原蛋白性关节炎有显著影响,但对抗胶原蛋白抗体水平无影响。由于胶原蛋白诱导的关节炎是一种据信T细胞和B细胞介导的免疫均起关键作用的疾病,体内抗独特型治疗对关节炎发展的当前作用可为研究独特型对B细胞和T细胞关节炎相关自身免疫的调节提供一个有趣的系统。