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CD40配体和白细胞介素-2对体外T细胞依赖性抗体形成的调节。

The regulation of T cell-dependent antibody formation in vitro by CD40 ligand and IL-2.

作者信息

Grabstein K H, Maliszewski C R, Shanebeck K, Sato T A, Spriggs M K, Fanslow W C, Armitage R J

机构信息

Department of Immunology, Immunex Research and Development Corporation, Seattle, WA 98101.

出版信息

J Immunol. 1993 Apr 15;150(8 Pt 1):3141-7.

PMID:7682232
Abstract

Our study demonstrates the central role for the murine CD40 ligand and IL-2 in contact-dependent T cell help for Ag-specific primary antibody responses in vitro. Helper T cell clones were found to express CD40 ligand after activation with CD3 mAb. Membrane-bound recombinant CD40 ligand expressed on fixed CV1/EBNA cells had similar B cell-activating properties as T cell clones that had been activated and then fixed. These activities include the induction of B cell proliferation, induction of polyclonal secretion of multiple Ig isotypes in a cytokine-dependent manner, and induction of Ag-specific antibody responses by purified B cells. The induction of polyclonal Ig secretion by the recombinant CD40 ligand required IL-4 and IL-5 although optimal Ag-specific antibody formation required IL-2. Finally, soluble CD40.Fc inhibited the induction of Ag-specific antibody responses by fixed, activated Th cell clones. The requirement for both CD40 ligand and IL-2 for induction of Ag-specific antibody responses was mediated, in part, by the induction of B cell IL-2R expression by CD40 ligand. We conclude that the interaction of CD40 on B cells with its ligand on activated T cells is an integral event in the early activation of B cells to grow and differentiate to antibody formation.

摘要

我们的研究证明了小鼠CD40配体和IL-2在体外抗原特异性初次抗体应答的接触依赖性T细胞辅助中起核心作用。在用CD3单克隆抗体激活后,发现辅助性T细胞克隆表达CD40配体。在固定的CV1/EBNA细胞上表达的膜结合重组CD40配体具有与已激活然后固定的T细胞克隆相似的B细胞激活特性。这些活性包括诱导B细胞增殖、以细胞因子依赖性方式诱导多种Ig同种型的多克隆分泌,以及由纯化的B细胞诱导抗原特异性抗体应答。重组CD40配体诱导多克隆Ig分泌需要IL-4和IL-5,尽管最佳的抗原特异性抗体形成需要IL-2。最后,可溶性CD40.Fc抑制了固定的、活化的Th细胞克隆诱导的抗原特异性抗体应答。CD40配体和IL-2对诱导抗原特异性抗体应答的需求部分是由CD40配体诱导B细胞IL-2R表达介导的。我们得出结论,B细胞上的CD40与其配体在活化T细胞上的相互作用是B细胞早期激活以生长并分化为抗体形成过程中的一个不可或缺的事件。

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