Boom W H, Liano D, Abbas A K
Department of Pathology, Brigham and Women's Hospital, Boston, Massachusetts.
J Exp Med. 1988 Apr 1;167(4):1350-63. doi: 10.1084/jem.167.4.1350.
To compare the helper function of murine T cell clones that secrete IL-2 and IFN-gamma (Th1 cells) or IL-4 and IL-5 (Th2), purified resting B cells were stimulated with F(ab')2 rabbit anti-mouse Ig (RAMG) and rabbit Ig-specific, class II MHC-restricted cloned T cells belonging to the two subsets. Both Th2 clones examined induced strong proliferative responses of B cells in the presence of RAMG, as well as the secretion of IgM and IgG1 antibodies. In contrast, the Th1 clones tested failed to stimulate B cell growth or antibody secretion. Th2-mediated B cell activation was dependent on IL-4 and IL-5, and was also inhibited by IFN-gamma or IFN-gamma produced by Th1 cells present in the same cultures. However, the failure of Th1 cells to help resting B cells could not be reversed with neutralizing anti-IFN-gamma antibody. In addition to this inhibitory effect, IFN-gamma was required for the secretion of IgG2a antibody, particularly when B cells were stimulated with polyclonal activators such as LPS. Finally, both sets of T cell clones secreted lymphokines when stimulated with purified B cells and RAMG. These experiments demonstrate that T cells that differ in lymphokine production also differ in their ability to help B cells as a result of cognate interactions at low concentrations of antigens. Moreover, IL-4, IL-5, and IFN-gamma serve different roles in the T cell-dependent proliferative and differentiative responses of resting B lymphocytes.
为比较分泌白细胞介素-2(IL-2)和干扰素-γ(IFN-γ)的小鼠T细胞克隆(Th1细胞)或分泌IL-4和IL-5的T细胞克隆(Th2细胞)的辅助功能,用F(ab')2兔抗小鼠Ig(RAMG)以及属于这两个亚群的兔Ig特异性、II类主要组织相容性复合体(MHC)限制性克隆T细胞刺激纯化的静止B细胞。所检测的两个Th2克隆在存在RAMG的情况下均诱导B细胞产生强烈的增殖反应,以及IgM和IgG1抗体的分泌。相比之下,所检测的Th1克隆未能刺激B细胞生长或抗体分泌。Th2介导的B细胞活化依赖于IL-4和IL-5,并且也受到同一培养物中存在的Th1细胞产生的IFN-γ或IFN-γ的抑制。然而,Th1细胞不能辅助静止B细胞的情况不能用中和抗IFN-γ抗体逆转。除了这种抑制作用外,IgG2a抗体的分泌需要IFN-γ,特别是当B细胞用多克隆激活剂如脂多糖(LPS)刺激时。最后,当用纯化的B细胞和RAMG刺激时,两组T细胞克隆均分泌淋巴因子。这些实验表明,在低浓度抗原的同源相互作用下,淋巴因子产生不同的T细胞在辅助B细胞的能力上也存在差异。此外,IL-4、IL-5和IFN-γ在静止B淋巴细胞的T细胞依赖性增殖和分化反应中发挥不同作用。