Fischer A, Sterkers G, Charron D, Durandy A
Eur J Immunol. 1986 Sep;16(9):1111-6. doi: 10.1002/eji.1830160914.
We have previously shown that the interaction between influenza virus-specific helper T lymphocytes and B lymphocytes is HLA class II restricted (Fischer, A. et al., Eur. J. Immunol. 1985. 15: 620). In the present study, we used a panel of antibodies specific for the T4 and HLA-DR molecules to investigate the role of both structures in T-B lymphocyte interaction. Several anti-T4 monoclonal antibodies were shown to block the in vitro antibody production to A/Bangkok influenza virus while they were unable to inhibit the A/Bangkok-induced proliferation of specific helper T cell clones. Some anti-HLA-DR monoclonal antibodies inhibited the antibody production to A/Bangkok, the target of the inhibition being either monocytes or B lymphocytes. The incubation of helper T cell clones with an infra-inhibitory concentration of anti-T4 antibody and of B lymphocytes with an infra-inhibitory concentration of anti-HLA-DR antibody resulted in a mutual enhancement of inhibition. Such synergistic interactions were not observed using combinations of anti-T4 and anti-B membrane structures such as p35 or LFA-1 or anti-HLA-DR and anti-T membrane structures such as T11 or LFA-1. First, these results indicate that the T4 molecule plays an essential role in T-B cell interaction even when it is not absolutely required for T cell proliferation. Second, they strongly suggest that the T4 molecule directly interacts with HLA-DR at the B cell surface. Whether such interaction is required to enhance the stability of T3/T cell receptor-antigen plus HLA class II association or whether T4-HLA-DR may transduce a signal towards B lymphocytes that is required in B cell activation remains unknown.
我们先前已表明,流感病毒特异性辅助性T淋巴细胞与B淋巴细胞之间的相互作用受HLA II类分子限制(费舍尔,A.等人,《欧洲免疫学杂志》,1985年。15: 620)。在本研究中,我们使用了一组针对T4和HLA - DR分子的特异性抗体,以研究这两种结构在T - B淋巴细胞相互作用中的作用。几种抗T4单克隆抗体被证明可阻断体外针对A/曼谷流感病毒的抗体产生,而它们无法抑制A/曼谷诱导的特异性辅助性T细胞克隆的增殖。一些抗HLA - DR单克隆抗体抑制了针对A/曼谷的抗体产生,抑制的靶点要么是单核细胞,要么是B淋巴细胞。用亚抑制浓度的抗T4抗体孵育辅助性T细胞克隆,并用亚抑制浓度的抗HLA - DR抗体孵育B淋巴细胞,导致抑制作用相互增强。使用抗T4与抗B细胞膜结构(如p35或LFA - 1)的组合,或抗HLA - DR与抗T细胞膜结构(如T11或LFA - 1)的组合,未观察到这种协同相互作用。首先,这些结果表明,即使T4分子对于T细胞增殖不是绝对必需的,它在T - B细胞相互作用中也起着至关重要的作用。其次,它们强烈表明,T4分子直接与B细胞表面的HLA - DR相互作用。这种相互作用是增强T3/T细胞受体 - 抗原加HLA II类分子结合的稳定性所必需的,还是T4 - HLA - DR可能向B淋巴细胞转导B细胞激活所需的信号,目前尚不清楚。