Iribe H, Tarutani S, Koga T, Terato K, Nagai Y
Department of Biochemistry, Faculty of Dentistry, Kyushu University, Fukuoka.
Fukuoka Igaku Zasshi. 1992 May;83(5):216-25.
A species specific epitope on human type II collagen (CII) recognized with mAb, 2-60, was found to be localized on a cyanogen bromide-cleaved peptide (CB10) of human CII. To characterize the antibody response to the 2-60 epitope, we raised rabbit anti-idiotypic (Id) antibody against 2-60. The rabbit anti-2-60 Id antibody reacted not only with 2-60 mAb but also with 2-56 and 3-11 mAbs which were reactive with the epitopes related to the 2-60 epitope on CB10. The anti-Id antibody inhibited the binding of these three mAbs to human CII. Thus, rabbit anti-2-60 Id antibody recognized the cross-reactive idiotype expressed on 2-60, 2-56 and 3-11. The anti-2-60 Id antibody inhibited about thirty percent of the binding of polyclonal anti-human CII antibody derived from DBA/1J mice, thereby suggesting that the 2-60 idiotype might be expressed on a major fraction of the anti-human CII antibody. Immunization with the rabbit anti-2-60 Id antibody elicited antibody response to the 2-60 epitope, in DBA/1J (H-2q, Ighc), BALB/c (H-2d, Igha) and DBA/2 (H-2d, Ighc) mice. On the other hand, an epitope-specific antibody response induced by rabbit anti-Id antibody to 1-5 mAb reactive with a putative arthritogenic epitope on human CII was shown to be influenced by a single dominant gene, possibly the Igh gene. Our findings suggest that antibody responses against two distinct epitopes on human CII are probably regulated by different mechanisms.
用单克隆抗体2-60识别的人II型胶原(CII)上的一个物种特异性表位,被发现定位于人CII的一个溴化氰裂解肽(CB10)上。为了表征对2-60表位的抗体反应,我们制备了针对2-60的兔抗独特型(Id)抗体。兔抗2-60 Id抗体不仅与2-60单克隆抗体反应,还与2-56和3-11单克隆抗体反应,这两种单克隆抗体与CB10上与2-60表位相关的表位有反应。抗Id抗体抑制了这三种单克隆抗体与人CII的结合。因此,兔抗2-60 Id抗体识别在2-60、2-56和3-11上表达的交叉反应独特型。抗2-60 Id抗体抑制了约30%源自DBA/1J小鼠的多克隆抗人CII抗体的结合,从而表明2-60独特型可能在大部分抗人CII抗体上表达。用兔抗2-60 Id抗体免疫在DBA/1J(H-2q,Ighc)、BALB/c(H-2d,Igha)和DBA/2(H-2d,Ighc)小鼠中引发了对2-60表位的抗体反应。另一方面,兔抗Id抗体对与人CII上一个假定的致关节炎表位反应的1-5单克隆抗体诱导的表位特异性抗体反应,显示受一个单一显性基因(可能是Igh基因)影响。我们的发现表明,针对人CII上两个不同表位的抗体反应可能受不同机制调控。