Literature DB >> 2786500

A major peritoneal reservoir of precursors for intestinal IgA plasma cells.

F G Kroese1, E C Butcher, A M Stall, L A Herzenberg.   

Abstract

Studies presented examine the origin of IgA plasma cells in B lineage chimeric mice constructed by reconstituting lethally irradiated mice with a mixture of syngeneic bone marrow cells and peritoneal cells from Ig heavy chain allotype congenic donors. In these mice, essentially all B cells in spleen and Peyer's patches are derived from the bone marrow donor; however Ly-1 B lineage cells which have been mainly detected in the peritoneum are derived from the peritoneal cell donor. Surprisingly, roughly half of the IgA plasma cells in the lamina propria of the gut are also derived from the peritoneal cell donor, suggesting an important role for peritoneally-derived B cells in the mucosal immune response.

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Year:  1989        PMID: 2786500     DOI: 10.3109/08820138909112226

Source DB:  PubMed          Journal:  Immunol Invest        ISSN: 0882-0139            Impact factor:   3.657


  16 in total

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Review 4.  Warner-Lambert/Parke-Davis Award lecture. Cellular and molecular mechanisms that direct leukocyte traffic.

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Review 5.  Role of retinoic acid in the imprinting of gut-homing IgA-secreting cells.

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Review 7.  Manipulation of the glycan-specific natural antibody repertoire for immunotherapy.

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8.  Dietary fructooligosaccharides up-regulate immunoglobulin A response and polymeric immunoglobulin receptor expression in intestines of infant mice.

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9.  The human intestinal IgA response; burning questions.

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10.  Positive selection of anti-thy-1 autoreactive B-1 cells and natural serum autoantibody production independent from bone marrow B cell development.

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