4.8 Article

Impaired IgA class switching in APRIL-deficient mice

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NATL ACAD SCIENCES
DOI: 10.1073/pnas.0307348101

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  1. NIAID NIH HHS [R01 AI031136, AI31136, P01 AI031541, AI31541, U19 AI031541] Funding Source: Medline
  2. NIDDK NIH HHS [R01 DK047677, DK47677, DK43351, P30 DK043351] Funding Source: Medline

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The tumor necrosis factor (TNF) family member APRIL binds to the receptors BCMA on B cells and TACI on B and T cells. To investigate the role of APRIL in immunity, we generated APRIL-deficient mice. APRIL(-'-) mice have normal T and B lymphocyte development, normal T and B cell proliferation in vitro, but increased numbers of CD44(hi)CD62L(lo) CD4(+) effector/memory T cells and increased IgG responses to T-dependent antigens. Serum IgA levels were significantly decreased, and serum IgA antibody responses to mucosal immunization with TD antigens and to type 1 T-independent antigens were impaired in APRIL(-/-) mice. APRIL by itself induced IgA as well as IgG1 isotype switching in CD40-deficient IgM(+)IgD(+) sorted B cells. These results suggest that APRIL down-regulates T cell-dependent antibody responses and promotes IgA class switching.

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