Eddy N K, Apple R J, Michael J G
J Immunol. 1987 Mar 15;138(6):1693-8.
A monoclonal antibody (3C-7) specific for a determinant localized on the carboxy-terminus of the BSA molecule (P505-582) has been shown to cause suppression of the multispecific BSA antibody response if given i.v. before immunization. The fine binding specificity and the isotype subclass are not responsible for the suppression generated. Administration of 3C-7 i.v. results in the generation of a suppressor T cell that, when transferred into reconstituted irradiated mice, results in a diminished anti-BSA response. Suppression can be eliminated by panning T cells on idiotype (3C-7) coated plates, but not by panning on BSA, polyclonal anti-BSA antibodies, or MOPC 21. The action of the cell is antigen (BSA) specific. Idiotype-binding T cells reconstitute suppression and appear to be Lyt-1-2+. These observations demonstrate that a limited set of monoclonal antibodies directed against a single determinant on a protein molecule have the capacity to regulate the immune response to a multiplicity of determinants present on the same protein. These data support the concept of antibody-induced regulation by the induction of suppressor cells through idiotype recognition.
一种针对牛血清白蛋白(BSA)分子(P505 - 582)羧基末端定位的决定簇具有特异性的单克隆抗体(3C - 7)已被证明,如果在免疫前静脉注射,会导致多特异性BSA抗体反应受到抑制。产生抑制作用的原因并非精细结合特异性和同种型亚类。静脉注射3C - 7会导致产生一种抑制性T细胞,将其转移到经重建照射的小鼠体内时,会导致抗BSA反应减弱。通过在包被独特型(3C - 7)的平板上淘选T细胞可消除抑制作用,但在包被BSA、多克隆抗BSA抗体或MOPC 21的平板上淘选则无法消除。该细胞的作用具有抗原(BSA)特异性。与独特型结合的T细胞可重建抑制作用,且似乎是Lyt - 1 - 2 +。这些观察结果表明,一组有限的针对蛋白质分子上单个决定簇的单克隆抗体有能力调节对同一蛋白质上多种决定簇的免疫反应。这些数据支持通过独特型识别诱导抑制性细胞来实现抗体诱导调节的概念。