The role of integrins and coreceptors in refining thresholds for B-cell responses

被引:26
作者
Batista, Facundo D. [1 ]
Arana, Eloisa [1 ]
Barral, Patricia [1 ]
Carrasco, Yolanda R. [1 ]
Depoil, David [1 ]
Eckl-Dorna, Julia [1 ]
Fleire, Sebastian [1 ]
Howe, Kathy [1 ]
Vehlow, Anne [1 ]
Weber, Michele [1 ]
Treanor, Bebhinn [1 ]
机构
[1] Canc Res UK, London Res Inst, Lymphocyte Interact Lab, London WC2A 3PX, England
关键词
b cell; BCR; antigen; activation; affinity; cytoskeleton;
D O I
10.1111/j.1600-065X.2007.00540.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Despite compelling evidence that a large proportion of antigens encountered in vivo by B cells are membrane bound, the general view is that B cells are mainly activated by soluble antigens. This notion may have been biased somewhat over the years because the high affinity of the B-cell receptor (BCR) for soluble intact ligands allows efficient B-cell stimulation in vitro. In vivo, however, even soluble antigens are likely to be deposited on the surface of antigen-presenting cells, either by complement or Fc receptors in the form of immune complexes, thus becoming more potent stimulators of B-cell activation. In this framework, the BCR works in a complex environment of integrins and coreceptors, as well as the B-cell cytoskeleton. Over the last few years, we have focused on B-cell membrane-bound antigen recognition. Here, we discuss some of our findings in the context of what is currently known in this exciting new field.
引用
收藏
页码:197 / 213
页数:17
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