Nishioka Y, Lipsky P E
Harold C. Simmons Arthritis Research Center, University of Texas Southwestern Medical Center at Dallas 75235.
J Immunol. 1994 Aug 1;153(3):1027-36.
Interactions between CD40 on B cells and its ligand on activated T cells have been reported to play an important role in T cell-B cell collaboration. In this current study, a mAb against the human CD40 ligand (5c8) was used to investigate the impact of CD40-CD40 ligand interactions in the initial activation of normal human peripheral blood B cells and in subsequent proliferation and differentiation. B cells were activated by co-culture with anti-CD3-stimulated normal T cells. mAb against CD40 ligand blocked initial T cell-dependent B cell activation, as assessed by [3H]uridine incorporation and IL-2R expression. Subsequent B cell proliferation and differentiation were also inhibited by this mAb. In addition to its effect on B cell activation, 5c8 also inhibited the capacity of B cells to augment IL-2 production by anti-CD3 activated T cells, implying a role for CD40-CD40 ligand interactions in the accessory function of B cells. Despite the importance of CD40-CD40 ligand interactions in T cell-B cell collaboration, CD40 ligand-deficient T cell clones were found to induce initial activation of B cells and support Ig production. This effect was only marginally effected by mAb to LFA-1 and ICAM-1, suggesting that additional interaction molecules play a role in T cell-B cell collaboration. Taken together, the data indicate that CD40-CD40 ligand interactions plays an important role in T cell-dependent B cell activation and subsequent differentiation but additional interaction structures are also involved in T cell-B cell collaboration.
据报道,B细胞上的CD40与其配体在活化T细胞上的相互作用在T细胞与B细胞的协作中发挥重要作用。在本研究中,使用一种抗人CD40配体的单克隆抗体(5c8)来研究CD40 - CD40配体相互作用在正常人外周血B细胞初始活化以及随后的增殖和分化中的影响。通过与抗CD3刺激的正常T细胞共培养来激活B细胞。抗CD40配体的单克隆抗体阻断了初始的T细胞依赖性B细胞活化,这通过[3H]尿苷掺入和IL - 2R表达来评估。该单克隆抗体也抑制了随后的B细胞增殖和分化。除了对B细胞活化的作用外,5c8还抑制了B细胞增强抗CD3活化T细胞产生IL - 2的能力,这意味着CD40 - CD40配体相互作用在B细胞的辅助功能中发挥作用。尽管CD40 - CD40配体相互作用在T细胞 - B细胞协作中很重要,但发现缺乏CD40配体的T细胞克隆可诱导B细胞的初始活化并支持Ig产生。这种效应仅受到抗LFA - 1和ICAM - 1单克隆抗体的轻微影响,表明其他相互作用分子在T细胞 - B细胞协作中发挥作用。综上所述,数据表明CD40 - CD40配体相互作用在T细胞依赖性B细胞活化及随后的分化中起重要作用,但其他相互作用结构也参与T细胞 - B细胞协作。