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Cutting Edge: NADPH Oxidase Modulates MHC Class II Antigen Presentation by B Cells
Author(s) -
Victoria L. Crotzer,
Juan D. Matute,
Andrés A. Arias,
Heng Zhao,
Lawrence A. Quilliam,
Mary C. Dinauer,
Janice S. Blum
Publication year - 2012
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.1103080
Subject(s) - nadph oxidase , antigen presentation , mhc class ii , biology , phagocyte , epitope , intracellular , chronic granulomatous disease , microbiology and biotechnology , antigen processing , antigen , reactive oxygen species , immune system , t cell , major histocompatibility complex , immunology , phagocytosis
Phagocyte NADPH oxidase plays a key role in pathogen clearance via reactive oxygen species (ROS) production. Defects in oxidase function result in chronic granulomatous disease with hallmark recurrent microbial infections and inflammation. The oxidase's role in the adaptive immune response is not well understood. Class II presentation of cytoplasmic and exogenous Ag to CD4(+) T cells was impaired in human B cells with reduced oxidase p40(phox) subunit expression. Naturally arising mutations, which compromise p40(phox) function in a chronic granulomatous disease patient, also perturbed class II Ag presentation and intracellular ROS production. Reconstitution of patient B cells with a wild-type, but not a mutant, p40(phox) allele restored exogenous Ag presentation and intracellular ROS generation. Remarkably, class II presentation of epitopes from membrane Ag was robust in p40(phox)-deficient B cells. These studies reveal a role for NADPH oxidase and p40(phox) in skewing epitope selection and T cell recognition of self Ag.

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