Abstract
The predominance of IgA plasma cells within the mucosal immune system has been known for many years but the regulation of IgA responses at mucosal sites is still poorly understood. The tendency of mucosal B cells to switch to IgA is thought to be influenced both by local bacterial antigens and mitogens and by locally produced lymphokines that promote IgA responses. The B cell populations on which these stimulants act are, however, already distinct from those elsewhere in the body, having been selected for their ability to migrate to and within the mucosal immune system.
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Faria, A.M.C., Rao, T.D., Phillips-Quagliata, J.M. (1995). A New IgA Receptor Expressed on a Highly Activated Murine B Cell Lymphoma. In: Mestecky, J., Russell, M.W., Jackson, S., Michalek, S.M., Tlaskalová-Hogenová, H., Šterzl, J. (eds) Advances in Mucosal Immunology. Advances in Experimental Medicine and Biology, vol 371. Springer, Boston, MA. https://doi.org/10.1007/978-1-4615-1941-6_140
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