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首页> 外文期刊>The journal of immunology >Amplified follicular immune complex deposition in mice lacking the Fc receptor gamma-chain does not alter maturation of the B cell response.
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Amplified follicular immune complex deposition in mice lacking the Fc receptor gamma-chain does not alter maturation of the B cell response.

机译:在缺乏Fc受体γ链的小鼠中,放大的滤泡免疫复合物沉积不会改变B细胞反应的成熟度。

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The role of Ag-Ab complexes (or immune complexes; ICs) in the regulation of the maturation of the B cell immune response was investigated in mice perturbed in the deposition and retention of such complexes. Loss of surface expression of Fc gammaRI and Fc gammaRIII due to targeted disruption of the common FcR gamma-chain gene results in dramatically increased deposition of ICs on follicular dendritic cells (FDCs) in germinal centers (GCs), attributed to altered clearance of circulating ICs. Despite these changes in the trapping of ICs by FDCs, serum Ab production, V gene hypermutation, isotype class switching and Ab affinity maturation are overtly unaltered. Thus, substantially augmenting B cell cognate Ag density on FDCs does not alter the outcome of the maturation of the B cell response. The significance of this finding in terms of the currently accepted model for the generation of B cell memory is discussed.
机译:研究了Ag-Ab复合物(或免疫复合物; IC)在调节B细胞免疫反应成熟中的作用。由于共同FcRγ链基因的定向破坏,导致Fc gammaRI和Fc gammaRIII的表面表达丧失,导致IC在生发中心(GC)中的滤泡树突状细胞(FDC)上沉积的IC急剧增加,这归因于循环IC清除率的改变。尽管在FDC捕获IC的过程中发生了这些变化,但血清Ab生产,V基因超突变,同种型类别转换和Ab亲和力成熟仍未改变。因此,在FDC上实质上增加B细胞同源Ag的密度不会改变B细胞反应成熟的结果。根据当前公认的B细胞内存生成模型,讨论了这一发现的重要性。

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