4.6 Article

Cutting Edge: T Cell-Dependent Plasmablasts Form in the Absence of Single Differentiated CD4+ T Cell Subsets

Journal

JOURNAL OF IMMUNOLOGY
Volume 202, Issue 2, Pages 401-405

Publisher

AMER ASSOC IMMUNOLOGISTS
DOI: 10.4049/jimmunol.1801349

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Funding

  1. National Institutes of Health [R01 AI039614, R01 AI103760, R37 AI027998, T32 AI007313, F31 AI133716]
  2. Dennis W. Watson Fellowship from the University of Minnesota Microbiology and Immunology Department

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The T follicular helper (Tfh) cell subset of CD4(+) Th cells promotes affinity maturation by B cells in germinal centers. The contribution of other Th cell subsets to B cell responses has not been fully explored in vivo. We addressed this issue by analyzing the T cell-dependent B cell response to the protein Ag PE in mice lacking specific Th cell subsets. As expected, PE-specific germinal center B cell production required Tfh cells. However, Tfh, Th1, or Th17 cell-deficient mice produced as many PE-specific, isotype-switched plasmablasts as wild-type mice. This response depended on Th cell expression of CD154 and Ag presentation by B cells. These results indicate that many Th cell subsets can promote plasmablast formation by providing CD40 signals to naive B cells.

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