Mora J R, von Andrian U H
Gastrointestinal Unit, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts, USA.
Mucosal Immunol. 2008 Mar;1(2):96-109. doi: 10.1038/mi.2007.14. Epub 2008 Jan 23.
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 alpha4beta7 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.
黏膜组织中的大多数抗体分泌细胞(ASC)产生免疫球蛋白A(IgA),它是体内最丰富的免疫球蛋白,也是分泌物中发现的主要抗体类别。IgA-ASC在黏膜相关淋巴组织中分化,通常被认为是一类同质细胞群体。然而,迁移至小肠的IgA-ASC在迁移需求方面具有独特特征。这些IgA-ASC需要归巢分子α4β7和CCR9与其配体黏膜地址素细胞黏附分子-1和CCL25相互作用,后者在小肠中组成性表达。事实上,最近的研究表明,与其他黏膜区室中的IgA-ASC相比,针对小肠的IgA-ASC是在不同条件下产生的。此外,诱导IgA类别转换的机制也可能因IgA-ASC分化所在的组织而异。在此,我们描述黏膜区室中IgA-ASC分化所涉及的机制,特别是那些与肠道归巢IgA-ASC产生相关的机制。