Armitage R J, Maliszewski C R, Alderson M R, Grabstein K H, Spriggs M K, Fanslow W C
Department of Cellular Immunology, Immunex Research and Development Corporation, Seattle, WA 98101.
Semin Immunol. 1993 Dec;5(6):401-12. doi: 10.1006/smim.1993.1046.
B cells can be stimulated to proliferate and differentiate in response to cell-contact dependent signals provided by activated, but not resting, T cells. In the human system, antibodies specific for the surface antigen CD40 induce similar B cell responses. The cloning of a ligand for CD40, and the generation of reagents which can block the interaction of this ligand with its receptor, have demonstrated that the major component of the contact-dependent signal leading to B cell activation is CD40 ligand. Studies of individuals lacking functional CD40 ligand have indicated that signaling through CD40 is essential for immunoglobulin (Ig) heavy chain switching and the production of all isotypes other than IgM. In addition to its activities on B cells, CD40 ligand is stimulatory for cells of monocyte and T lineages suggesting a pleiotropic role for CD40 ligand in vivo.
活化而非静止的T细胞提供的细胞接触依赖性信号可刺激B细胞增殖和分化。在人体系统中,针对表面抗原CD40的特异性抗体可诱导类似的B细胞反应。CD40配体的克隆以及能够阻断该配体与其受体相互作用的试剂的产生,表明导致B细胞活化的接触依赖性信号的主要成分是CD40配体。对缺乏功能性CD40配体的个体的研究表明,通过CD40发出信号对于免疫球蛋白(Ig)重链转换以及除IgM以外的所有同种型的产生至关重要。除了对B细胞有作用外,CD40配体对单核细胞和T细胞系的细胞也有刺激作用,这表明CD40配体在体内具有多效性作用。