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

Journal

IMMUNOLOGICAL REVIEWS
Volume 218, Issue -, Pages 197-213

Publisher

BLACKWELL PUBLISHING
DOI: 10.1111/j.1600-065X.2007.00540.x

Keywords

b cell; BCR; antigen; activation; affinity; cytoskeleton

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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.

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