Lane P, Burdet C, McConnell F, Lanzavecchia A, Padovan E
Basel Institute for Immunology, Switzerland.
Eur J Immunol. 1995 Jun;25(6):1788-93. doi: 10.1002/eji.1830250646.
We report the capacity of CD40 ligand (CD40L)-negative T cell clones to activate human B cells. CD40L-negative T cells induce a level of B cell proliferation 10-20% of that seen with normal T cells. The signal provided by the negative clones is synergistic with that derived from a CD40L transfectant, and restores B cell proliferation to normal levels, showing that CD40L-negative T cell clones are not inherently inhibitory for B cells. Although their capacity to induce proliferation was much reduced, CD40L-negative T cell clones were still strong inducers of B cell differentiation to plasma cells. This differentiation to plasma cells was inhibited by a CD40L transfectant. The data are discussed with regard to the normal in vivo mechanism for maintaining B cell memory and memory antibody responses to T-dependent antigens.
我们报告了CD40配体(CD40L)阴性T细胞克隆激活人B细胞的能力。CD40L阴性T细胞诱导的B细胞增殖水平为正常T细胞的10%-20%。阴性克隆提供的信号与来自CD40L转染子的信号具有协同作用,并将B细胞增殖恢复到正常水平,表明CD40L阴性T细胞克隆对B细胞并非固有抑制作用。尽管其诱导增殖的能力大大降低,但CD40L阴性T细胞克隆仍是B细胞分化为浆细胞的强力诱导剂。这种向浆细胞的分化受到CD40L转染子的抑制。我们将结合维持B细胞记忆和对T依赖性抗原的记忆抗体反应的正常体内机制来讨论这些数据。