Pierce S K, Cancro M P, Klinman N R
J Exp Med. 1978 Sep 1;148(3):759-65. doi: 10.1084/jem.148.3.759.
In recent years antigen-specific T cells have been shown to be capable of mediating a number of diverse functions in collaboration with B cells in humoral immune responses. One of the more intriguing roles attributed to helper T cells is the promotion of the synthesis of multiple immunoglobulin isotypes by B cells in T-dependent antibody responses. The experiments presented in this report were carried out to determine if an individual antigen-specific T lymphocyte has the capability to enable the production of antibodies of multiple immunoglobulin heavy chain isotypes. We describe an experimental system which allows for the isolation and antigenic stimulation of individual helper T cells in a splenic environment which provides an excess of primary B cells for collaboration with isolated T lymphocytes. Employing this system we have demonstrated that an individual antigen-specific T lymphocyte, specific for the PR8 strain of influenza virus, has the capacity to enable primary B-cell PR8-specific antibody responses of more than a single immunoglobulin isotype. The implications made by these studies regarding the problem of genetic restrictions regulating T-cell-B-cell interaction is discussed.
近年来,抗原特异性T细胞已被证明能够在体液免疫反应中与B细胞协作介导多种不同功能。辅助性T细胞的一个更有趣的作用是在T细胞依赖性抗体反应中促进B细胞合成多种免疫球蛋白同种型。本报告中所呈现的实验旨在确定单个抗原特异性T淋巴细胞是否有能力促使产生多种免疫球蛋白重链同种型的抗体。我们描述了一种实验系统,该系统允许在脾脏环境中分离和抗原刺激单个辅助性T细胞,该环境提供了过量的初始B细胞以与分离的T淋巴细胞协作。利用该系统,我们已经证明,针对流感病毒PR8株的单个抗原特异性T淋巴细胞有能力促使初始B细胞产生针对PR8的、不止一种免疫球蛋白同种型的特异性抗体反应。讨论了这些研究对于调节T细胞 - B细胞相互作用的遗传限制问题的启示。