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B Cells Regulate CD4+ T Cell Responses to Papain following B Cell Receptor–Independent Papain Uptake
Author(s) -
Daniel F. Dwyer,
Matthew C. Woodruff,
Michael C. Carroll,
K. Frank Austen,
Michael F. Gurish
Publication year - 2014
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.1303247
Subject(s) - papain , adjuvant , cysteine protease , microbiology and biotechnology , internalization , b cell , immune system , chemistry , receptor , biology , protease , immunology , antibody , biochemistry , enzyme
Papain, a cysteine protease allergen with inherent adjuvant activity, induces potent IL-4 expression by T cells in the popliteal lymph nodes of mice following footpad immunization. In this study, we identify a novel, non-BCR-mediated capacity for B cells to rapidly bind and internalize papain. B cells subsequently regulate the adaptive immune response by enhancing ICOS expression on CD4(+) T cells and amplifying Th2 and follicular helper T cell induction. Ab blockade of ICOS ligand, expressed by popliteal lymph node B cells, but not dendritic cells, at the peak of the response inhibits IL-4 responses in wild-type mice but not B cell-deficient mice. Thus, B cells play a critical role in amplifying adjuvant-dependent Th2 polarization following noncanonical acquisition and internalization of the cysteine protease papain.

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