Iribe H, Kabashima H, Koga T
Department of Biochemistry, Kyushu University School of Dentistry, Fukuoka, Japan.
J Immunol. 1989 Mar 1;142(5):1487-94.
We reported the presence of three distinct epitopes commonly present on murine and human type II collagen (CII), observed using mAb. To investigate the possible involvement of these epitopes in collagen-induced arthritis, we raised rabbit anti-idiotypic antibodies that may bear the internal image of these epitopes. Anti-idiotypic antibodies developed against three anti-CII mAb designated as 1-5, 2-14, and 2-15 were demonstrated to recognize idiotype expressed on Ag-binding site (paratope) of their related mAb. Anti-CII antibody response specific for a given epitope could be induced in DBA/1J mice upon immunization with anti-idiotypic antibodies coupled to keyhole limpet hemocyanin. Anti-idiotypic antibody to 1-5 antibody in particular could stimulate all DBA/1J mice for production of anti-CII antibody possessing Ag specificity and idiotype similar to those of 1-5 antibody. Although the mice immunized with anti-1-5 antibody alone did not develop arthritis, they did show a much more enhanced antibody response against a given epitope than did control mice non-treated with anti-idiotypic antibody upon the subsequent immunization with human CII. Some of the mice immunized with anti-1-5 antibody and challenged with human CII developed arthritis, whereas the control mice did not. These findings strongly suggest that a common epitope recognized by 1-5 antibody might be involved in the induction of arthritis.
我们报告了使用单克隆抗体(mAb)观察到的在小鼠和人类II型胶原蛋白(CII)上普遍存在的三种不同表位。为了研究这些表位可能在胶原诱导的关节炎中的作用,我们制备了可能带有这些表位内影像的兔抗独特型抗体。针对三种抗CII单克隆抗体(分别命名为1-5、2-14和2-15)产生的抗独特型抗体被证明能够识别与其相关单克隆抗体的抗原结合位点(互补决定区)上表达的独特型。在用与钥孔血蓝蛋白偶联的抗独特型抗体免疫后,DBA/1J小鼠中可诱导出针对给定表位的抗CII抗体反应。特别是针对1-5抗体的抗独特型抗体能够刺激所有DBA/1J小鼠产生具有与1-5抗体相似的抗原特异性和独特型的抗CII抗体。虽然单独用抗1-5抗体免疫的小鼠没有发生关节炎,但在随后用人CII免疫时,它们针对给定表位的抗体反应比未用抗独特型抗体处理的对照小鼠增强得多。一些用抗1-5抗体免疫并用人类CII攻击的小鼠发生了关节炎,而对照小鼠则没有。这些发现强烈表明,1-5抗体识别的一个共同表位可能参与了关节炎的诱导。