Cronin D C, Stack R, Fitch F W
Committee on Immunology, University of Chicago, IL 60637.
J Immunol. 1995 Apr 1;154(7):3118-27.
Interactions between CD4+ T cells and B cells are mediated by both soluble factors and cell surface molecules. The Ag-independent interaction between the CD40 ligand, expressed on activated T cells, and its CD40 receptor, expressed on B cells, enhances B cell proliferation in response to IL-4 stimulation. The expression of the CD40 ligand is induced on CD4+ T cells by stimulation with Ag-pulsed APC or mitogens. Here, we show that at least some IL-4-producing murine CD8+ T cell clones can be induced to express the CD40 ligand when stimulated with anti-CD3 mAb. Additionally, such activated CD8+ IL-4-producing clones potentiate the proliferative response of small resting B cells to IL-4 and induce Ig secretion by small resting B cells to IL-4 and IL-5. Proliferation of small resting B cells cultured with IL-4 in the presence of activated IL-4-producing CD8+ murine T cell clones appeared to be mediated by the expression of the CD40 ligand on the T cell because an anti-CD40 ligand mAb inhibited this proliferative response. A conventional murine CD8+ CTL clone, which did not produce IL-4 or express CD40 ligand upon activation, did not potentiate proliferation of small resting B cells exposed to IL-4. Thus, under some circumstances, CD8+ T cells that are able to express CD40 ligand may be able to provide B cell help.
CD4+ T细胞与B细胞之间的相互作用是由可溶性因子和细胞表面分子介导的。活化T细胞上表达的CD40配体与其在B细胞上表达的CD40受体之间的非抗原依赖性相互作用,增强了B细胞对IL-4刺激的增殖反应。通过用抗原脉冲的抗原呈递细胞(APC)或丝裂原刺激,可诱导CD4+ T细胞上CD40配体的表达。在此,我们表明,当用抗CD3单克隆抗体刺激时,至少一些产生IL-4的小鼠CD8+ T细胞克隆可被诱导表达CD40配体。此外,这种活化的产生IL-4的CD8+克隆增强了静止小B细胞对IL-4的增殖反应,并诱导静止小B细胞对IL-4和IL-5分泌免疫球蛋白。在活化的产生IL-4的CD8+小鼠T细胞克隆存在的情况下,用IL-4培养的静止小B细胞的增殖似乎是由T细胞上CD40配体的表达介导的,因为抗CD40配体单克隆抗体抑制了这种增殖反应。一个传统的小鼠CD8+细胞毒性T淋巴细胞(CTL)克隆,在活化时不产生IL-4或不表达CD40配体,不能增强暴露于IL-4的静止小B细胞的增殖。因此,在某些情况下,能够表达CD40配体的CD8+ T细胞可能能够提供B细胞辅助。