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Mucosal Immunol ; 12(5): 1082-1091, 2019 09.
Article in English | MEDLINE | ID: mdl-31142830

ABSTRACT

Leukotriene B4 receptor 1 (BLT1) triggers the migration of granulocytes and activated T cells; however, its role in B-cell function remains unclear. Here we report that BLT1 is required to induce the production of antigen-specific IgA against oral vaccine through mediating innate immune signals from commensal bacteria. B cells acquire BLT1 expression during their differentiation to IgA+ B cells and plasma cells in Peyer's patches and the small intestinal lamina propria, respectively. BLT1 KO mice exhibited impaired production of antigen-specific fecal IgA to oral vaccine despite normal IgG responses to systemically immunized antigen. Expression of MyD88 was decreased in BLT1 KO gut B cells and consequently led to diminished proliferation of commensal bacteria-dependent plasma cells. These results indicate that BLT1 enhances the proliferation of commensal bacteria-dependent IgA+ plasma cells through the induction of MyD88 and thereby plays a key role in the production of antigen-specific intestinal IgA.


Subject(s)
Epitopes/immunology , Gastrointestinal Microbiome/immunology , Immunity, Innate , Immunoglobulin A, Secretory/immunology , Intestinal Mucosa/immunology , Intestinal Mucosa/metabolism , Receptors, Leukotriene B4/genetics , Animals , B-Lymphocytes/immunology , B-Lymphocytes/metabolism , Immunization , Intestinal Mucosa/microbiology , Male , Mice , Mice, Knockout , Myeloid Differentiation Factor 88/metabolism , Peyer's Patches/immunology , Peyer's Patches/metabolism , Plasma Cells/immunology , Plasma Cells/metabolism , Receptors, Leukotriene B4/metabolism , Signal Transduction , Vaccines/administration & dosage , Vaccines/immunology
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