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首页> 外文期刊>The journal of immunology >Cutting Edge: B Cells Promote CD8+ T Cell Activation in MRL-Faslpr Mice Independently of MHC Class I Antigen Presentation
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Cutting Edge: B Cells Promote CD8+ T Cell Activation in MRL-Faslpr Mice Independently of MHC Class I Antigen Presentation

机译:前沿:B细胞在MRL-Faslpr小鼠中促进CD8 + T细胞活化,独立于MHC I类抗原呈递

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摘要

Spontaneous CD8+ T cell activation in MRL- Fas lpr mice is B cell dependent. It is unclear whether this B-dependent activation is mediated by direct Ag presentation via MHC class I proteins (i.e., cross-presentation) or whether activation occurs by an indirect mechanism, e.g., via effects on CD4+ cells. To determine how CD8+ T cell activation is promoted by B cells, we created mixed bone marrow chimeras where direct MHC class I Ag presentation by B cells was abrogated while other leukocyte compartments could express MHC class I. Surprisingly, despite the absence of B cell class I-restricted Ag presentation, CD8+ T cell activation was intact in the chimeric mice. Therefore, the spontaneous B cell-dependent CD8+ T cell activation that occurs in systemic autoimmunity is not due to direct presentation by B cells to CD8+ T cells.
机译:MRL-Fas lpr小鼠中自发性CD8 + T细胞活化是B细胞依赖性的。目前尚不清楚这种B依赖性激活是通过经由MHC I类蛋白的直接Ag呈递来介导的(即交叉呈递),还是由间接机制(例如,通过对CD4 +细胞的影响)发生。为了确定B细胞如何促进CD8 + T细胞活化,我们创建了混合的骨髓嵌合体,其中废除了B细胞对MHC I类的直接抗原呈递,而其他白细胞区室可以表达I类MHC。令人惊讶的是,尽管缺乏B细胞类我限制了Ag的表达,在嵌合小鼠中CD8 + T细胞的激活是完整的。因此,在全身性自身免疫中发生的自发性B细胞依赖性CD8 + T细胞活化不是由于B细胞直接呈递给CD8 + T细胞。

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