IgA-mediated control of host-microbial interaction during weaning reaction influences gut inflammation.

The mechanisms of how host-microbe mutualistic relationships are established at weaning contingently upon B-cell surveillance remain inadequately elucidated. We found that CD138 + plasmacyte (PC)-mediated promotion of IgA response regulates the symbiosis between Bacteroides uniformis ( B. uniformis ) and the host during the weaning period. The IgA-skewed response of CD138 + PCs is essential for B. uniformis to occupy a defined gut luminal niche, thereby fostering stable colonization. Furthermore, B. uniformis within the natural gut niche was perturbed in the absence of IgA, resulting in exacerbated gut inflammation in IgA-deficient mice and weaned piglets. Thus, we propose that the priming and maintenance of intestinal IgA response from CD138 + PCs are required for host-microbial symbiosis, whereas the perturbation of which would enhance inflammation in weaning process.