Rey Jacques, Garin Nathalie, Spertini François, Corthésy Blaise
Laboratoire de Recherche et Développement, du Service d'Immunologie et d'Allergie, Centre Hospitalier Universitaire Vaudois, Lausanne, Switzerland.
J Immunol. 2004 Mar 1;172(5):3026-33. doi: 10.4049/jimmunol.172.5.3026.
In addition to being instrumental to the protection of mucosal epithelia, secretory IgA (SIgA) adheres to and is transported by intestinal Peyer's patch (PP) M cells. The possible functional reason for this transport is unknown. We have thus examined in mice the outcome of SIgA delivered from the intestinal lumen to the cells present in the underlying organized mucosa-associated lymphoreticular tissue. We show selective association of SIgA with dendritic cells and CD4(+) T and B lymphocytes recovered from PP in vitro. In vivo, exogenously delivered SIgA is able to enter into multiple PP lining the intestine. In PP, SIgA associates with and is internalized by dendritic cells in the subepithelial dome region, whereas the interaction with CD4(+) T cells is limited to surface binding. Interaction between cells and SIgA is mediated by the IgA moiety and occurs for polymeric and monomeric molecular forms. Thus, although immune exclusion represents the main function of SIgA, transport of the Ab by M cells might promote Ag sampling under neutralizing conditions essential to the homeostasis of mucosal surfaces.
除了有助于保护黏膜上皮外,分泌型IgA(SIgA)还能黏附于肠道派尔集合淋巴结(PP)的M细胞并由其转运。这种转运可能的功能原因尚不清楚。因此,我们在小鼠中研究了从肠腔递送至下方有组织的黏膜相关淋巴组织中的细胞的SIgA的结果。我们发现,在体外从PP中回收的树突状细胞以及CD4(+) T和B淋巴细胞与SIgA存在选择性关联。在体内,外源性递送的SIgA能够进入肠道内多个PP。在PP中,SIgA与上皮下圆顶区域的树突状细胞结合并被其内化,而与CD4(+) T细胞的相互作用仅限于表面结合。细胞与SIgA之间的相互作用由IgA部分介导,且聚合物和单体分子形式均会发生。因此,尽管免疫排斥是SIgA的主要功能,但M细胞对抗体的转运可能会在对黏膜表面稳态至关重要的中和条件下促进抗原采样。
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