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Differentiation and homing of IgA-secreting cells

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MUCOSAL IMMUNOLOGY
卷 1, 期 2, 页码 96-109

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NATURE PUBLISHING GROUP
DOI: 10.1038/mi.2007.14

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  1. Crohn's & Colitis Foundation of America (CCFA)
  2. Cancer Research Institute (CRI)
  3. Center for the Study of Inflammatory Bowel Disease [DK43351]
  4. NIH

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Most antibody-secreting cells (ASCs) in mucosal tissues produce immunoglobulin A (IgA), the most abundant immunoglobulin in the body and the main class of antibody found in secretions. IgA-ASCs differentiate in the mucosal-associated lymphoid tissues and are usually considered as a homogeneous population of cells. However, IgA-ASCs that travel to the small intestine have unique characteristics in terms of their migratory requirements. These IgA-ASCs require the homing molecules alpha 4 beta 7 and CCR9 to interact with their ligands, mucosal addressin cell adhesion molecule-1 and CCL25, which are constitutively expressed in the small intestine. Indeed, recent work has shown that IgA-ASCs specific for the small bowel are generated under different conditions as compared with IgA-ASCs in other mucosal compartments. Moreover, the mechanisms inducing IgA class switching may also vary according to the tissue where IgA-ASCs differentiate. Here we describe the mechanisms involved in the differentiation of IgA-ASCs in mucosal compartments, in particular those involved in the generation of gut-homing IgA-ASCs.

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