Suppr超能文献

辅助性T细胞依赖的静止B细胞分化诱导不一定需要同源细胞相互作用。

T helper cell-dependent induction of resting B cell differentiation need not require cognate cell interactions.

作者信息

Julius M H, Rammensee H G

机构信息

Department of Immunology, McGill University, Montreal, Basel Institute for Immunology, Quebec, Canada.

出版信息

Eur J Immunol. 1988 Mar;18(3):375-9. doi: 10.1002/eji.1830180309.

Abstract

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.

摘要

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。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验