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Antigen presentation by dendritic cells for B cell activation.
Heath, William R; Kato, Yu; Steiner, Thiago M; Caminschi, Irina.
Afiliação
  • Heath WR; Department of Microbiology and Immunology, The Doherty Institute for Infection and Immunity, The University of Melbourne, Victoria, 3010, Australia; Australian Research Council Centre of Excellence in Advanced Molecular Imaging, University of Melbourne, Victoria, 3010, Australia. Electronic address:
  • Kato Y; Department of Microbiology and Immunology, The Doherty Institute for Infection and Immunity, The University of Melbourne, Victoria, 3010, Australia; Australian Research Council Centre of Excellence in Advanced Molecular Imaging, University of Melbourne, Victoria, 3010, Australia.
  • Steiner TM; Department of Microbiology and Immunology, The Doherty Institute for Infection and Immunity, The University of Melbourne, Victoria, 3010, Australia; Australian Research Council Centre of Excellence in Advanced Molecular Imaging, University of Melbourne, Victoria, 3010, Australia.
  • Caminschi I; Infection and Immunity Program, Monash Biomedicine Discovery Institute and Department of Biochemistry and Molecular Biology, Monash University, Clayton, Victoria, 3168, Australia. Electronic address: irina.caminschi@monash.edu.
Curr Opin Immunol ; 58: 44-52, 2019 06.
Article em En | MEDLINE | ID: mdl-31071588
ABSTRACT
B cells are efficiently activated by antigens presented on cell membranes, which provide opportunity for receptor cross-linking and antigen capture. The two main cell types implicated in native antigen presentation to B cells are follicular dendritic cells (FDC), which reside in B cell follicles, and CD169+ macrophages, which line the antigen-exposed surfaces of these follicles in both the lymph nodes and the spleen. There is mounting evidence, however, that conventional dendritic cells (cDC) can also participate in native antigen presentation to B cells. This underappreciated role, largely hidden by the simultaneous need for cDC to participate in T cells priming, appears to be primarily mediated by the type 2 subset of cDC (cDC2), but may also be a function of cDC1. Better understanding of how cDC participate in B cell priming is likely to improve our capacity to develop effective humoral vaccines.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Células Dendríticas / Linfócitos B / Ativação Linfocitária / Linfócitos T / Apresentação de Antígeno Limite: Animals / Humans Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Células Dendríticas / Linfócitos B / Ativação Linfocitária / Linfócitos T / Apresentação de Antígeno Limite: Animals / Humans Idioma: En Ano de publicação: 2019 Tipo de documento: Article