Julius M H, Rammensee H G
Department of Immunology, McGill University, Montreal, Basel Institute for Immunology, Quebec, Canada.
Eur J Immunol. 1988 Mar;18(3):375-9. doi: 10.1002/eji.1830180309.
We have analyzed the role of cognate interaction with helper T cells (Th) in support of resting B cell differentiation to plaque formation. Co-culture of histoincompatible resting B cells and resting Th cells resulted in the induction of plaque-forming cells when dimeric but not monomeric fragments of anti-T cell receptor (TcR) antibody were added to culture. The efficiency of B cell activation was comparable to that supported by lipopolysaccharide and lectin-mediated Th-B cell conjugate formation. Further, if resting Th cells were preactivated with antigen and histocompatible antigen-presenting cells, the requirement for addition of anti-TcR to mixtures of histoincompatible Th and B cells was obviated. These results demonstrate that TcR-mediated Th recognition of major histoincompatibility complex class II/antigen composites on the resting B cell membrane does not provide obligate signals for B cell differentiation to plaque formation. We are left with two possibilities. Either the entire process of Th cell-dependent induction of resting B cell differentiation is mediated by soluble lymphokines or if Th-B cell contact is mandatory, it is mediated through nonpolymorphic cell surface determinants.
我们分析了同源辅助性T细胞(Th)相互作用在支持静止B细胞分化为噬斑形成细胞过程中的作用。当将抗T细胞受体(TcR)抗体的二聚体而非单体片段添加到培养物中时,组织不相容的静止B细胞与静止Th细胞共培养可诱导噬斑形成细胞的产生。B细胞激活的效率与脂多糖和凝集素介导的Th - B细胞共轭形成所支持的效率相当。此外,如果用抗原和组织相容性抗原呈递细胞对静止Th细胞进行预激活,则在组织不相容的Th细胞和B细胞混合物中添加抗TcR的需求就可以消除。这些结果表明,TcR介导的Th细胞对静止B细胞膜上主要组织相容性复合体II类/抗原复合物的识别,并不是B细胞分化为噬斑形成细胞的必要信号。我们面临两种可能性。要么静止B细胞分化的Th细胞依赖性诱导的整个过程由可溶性淋巴细胞因子介导,要么如果Th - B细胞接触是必需的,那么它是通过非多态性细胞表面决定簇介导的。