van den Eertwegh A J, Laman J D, Noelle R J, Boersma W J, Claassen E
Department of Immunological and Infectious Diseases, TNO Prevention and Health, The Netherlands.
Semin Immunol. 1994 Oct;6(5):327-36. doi: 10.1006/smim.1994.1041.
T-B cell interactions have a central role in the development of humoral immunity. The binding of a 39 kDa protein (gp39), selectively expressed on activated Th cells, to its receptor CD40, on B cells, results in the initial B cell activation. Thereafter, Th cell derived cytokines regulate the differentiation of B cells into antibody-forming cells. Most of these data are derived from in vitro experiments. This article discusses in vivo experiments dealing with T-B interactions. First, the immunohistochemical analysis of T cell activation (gp39 expression), cytokine and antibody production in murine spleens after injection of model antigens (TNP-Ficoll, TNP-KLH, and rabbit anti-IgD antibodies). Second, the in vivo role of gp39 and cytokines in these immune responses. Finally, by combining these in vivo experiments with in vitro data we present an in vivo model for T cell dependent antibody responses.
T细胞与B细胞的相互作用在体液免疫的发展中起着核心作用。活化的Th细胞上选择性表达的一种39 kDa蛋白(gp39)与B细胞上的受体CD40结合,导致B细胞的初始活化。此后,Th细胞衍生的细胞因子调节B细胞分化为抗体形成细胞。这些数据大多来自体外实验。本文讨论了关于T细胞与B细胞相互作用的体内实验。首先,对注射模型抗原(TNP-菲可、TNP-钥孔戚血蓝蛋白和兔抗IgD抗体)后小鼠脾脏中T细胞活化(gp39表达)、细胞因子和抗体产生进行免疫组织化学分析。其次,gp39和细胞因子在这些免疫反应中的体内作用。最后,通过将这些体内实验与体外数据相结合,我们提出了一个T细胞依赖性抗体反应的体内模型。