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B Cell Antigen Presentation in the Initiation of Follicular Helper T Cell and Germinal Center Differentiation

机译:滤泡辅助性T细胞和生殖中心分化中B细胞抗原的呈递

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High-affinity class-switched Abs and memory B cells are products of the germinal center (GC). The CD4+ T cell help required for the development and maintenance of the GC is delivered by follicular Th cells (TFH), a CD4+ Th cell subset characterized by expression of Bcl-6 and secretion of IL-21. The cellular interactions that mediate differentiation of TFH and GC B cells remain an important area of investigation. We previously showed that MHC class II (MHCII)–dependent dendritic cell Ag presentation is sufficient for the differentiation of a TFH intermediate (termed pre-TFH), characterized by Bcl-6 expression but lacking IL-21 secretion. In this article, we examine the contributions of MHCII Ag presentation by B cells to TFH differentiation and GC responses in several contexts. B cells alone do not efficiently prime naive CD4+ T cells or induce TFH after protein immunization; however, during lymphocytic choriomeningitis virus infection, B cells induce TFH differentiation despite the lack of effector CD4+ T cell generation. Still, MHCII+ dendritic cells and B cells cooperate for optimal TFH and GC B cell differentiation in response to both model Ags and viral infection. This study highlights the roles for B cells in both CD4+ T cell priming and TFH differentiation, and demonstrates that different APC subsets work in tandem to mediate the GC response.
机译:高亲和力的类转换Abs和记忆B细胞是生发中心(GC)的产物。卵泡Th细胞(TFH)提供了发育和维持GC所需的CD4 + T细胞帮助,该细胞是特征为Bcl-6表达和IL-21分泌的CD4 + Th细胞亚群。介导TFH和GC B细胞分化的细胞相互作用仍然是重要的研究领域。我们先前显示,依赖MHC II类(MHCII)的树突状细胞Ag呈递足以分化以Bcl-6表达但缺乏IL-21分泌为特征的TFH中间体(称为pre-TFH)。在本文中,我们研究了几种情况下B细胞对MHCII Ag的表达对TFH分化和GC反应的贡献。单独的B细胞不能有效地引发天然CD4 + T细胞或蛋白质免疫后诱导TFH。然而,在淋巴细胞性脉络膜脑膜炎病毒感染期间,尽管缺乏效应子CD4 + T细胞的产生,B细胞仍能诱导TFH分化。尽管如此,MHCII +树突状细胞和B细胞仍可协同响应模型Ags和病毒感染,从而实现最佳的TFH和GC B细胞分化。这项研究突出了B细胞在CD4 + T细胞启动和TFH分化中的作用,并证明了不同的APC亚组协同作用来介导GC反应。

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