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Plasma cells negatively regulate the follicular helper T cell program.


ABSTRACT: B lymphocytes differentiate into antibody-secreting cells under the antigen-specific control of follicular helper T cells (T(FH) cells). Here we demonstrate that isotype-switched plasma cells expressed major histocompatibility complex (MHC) class II, the costimulatory molecules CD80 and CD86, and the intracellular machinery required for antigen presentation. Antigen-specific plasma cells accessed, processed and presented sufficient antigen in vivo to induce multiple helper T cell functions. Notably, antigen-primed plasma cells failed to induce interleukin 21 (IL-21) or the transcriptional repressor Bcl-6 in naive helper T cells and actively decreased these key molecules in antigen-activated T(FH) cells. Mice lacking plasma cells showed altered T(FH) cell activity, which provided evidence of this negative feedback loop. Hence, antigen presentation by plasma cells defines a previously unknown layer of cognate regulation that limits the antigen-specific T(FH) cell program that controls ongoing B cell immunity.

SUBMITTER: Pelletier N 

PROVIDER: S-EPMC3058870 | biostudies-literature | 2010 Dec

REPOSITORIES: biostudies-literature

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Plasma cells negatively regulate the follicular helper T cell program.

Pelletier Nadége N   McHeyzer-Williams Louise J LJ   Wong Kurt A KA   Urich Eduard E   Fazilleau Nicolas N   McHeyzer-Williams Michael G MG  

Nature immunology 20101031 12


B lymphocytes differentiate into antibody-secreting cells under the antigen-specific control of follicular helper T cells (T(FH) cells). Here we demonstrate that isotype-switched plasma cells expressed major histocompatibility complex (MHC) class II, the costimulatory molecules CD80 and CD86, and the intracellular machinery required for antigen presentation. Antigen-specific plasma cells accessed, processed and presented sufficient antigen in vivo to induce multiple helper T cell functions. Nota  ...[more]

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