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Helper B Cells Promote Cytotoxic T Cell Survival and Proliferation Independently of Antigen Presentation through CD27/CD70 Interactions
Author(s) -
Sara Deola,
Monica C. Panelli,
Dragan Maric,
Silvia Selleri,
Natalia I. Dmitrieva,
Ching Y. Voss,
Harvey G. Klein,
David Stroncek,
Ena Wang,
Francesco M. Marincola
Publication year - 2008
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.180.3.1362
Subject(s) - cytotoxic t cell , priming (agriculture) , antigen presenting cell , microbiology and biotechnology , proinflammatory cytokine , biology , epitope , t cell , antigen presentation , immunology , interleukin 21 , ctl* , cd40 , cd8 , antigen , inflammation , immune system , in vitro , biochemistry , botany , germination
CD8-expressing cytotoxic T cell (CTL) interactions with APCs and helper T cells determine their function and ability to survive. In this study, we describe a novel interaction independent of Ag presentation between activated CTLs and bystander CD19-expressing B lymphocytes. Ag-stimulated CTLs serially engage autologous B lymphocytes through CD27/CD70 contact that promotes their survival and proliferation. Moreover, these interactions induce the release of proinflammatory cytokines that follows two general patterns: 1) an epitope-dependent enhancement of cytokine release, and 2) a previously undiscovered coordinate release of cytokines independent of epitope exposure. The latter includes chemoattractants targeting activated T cells. As a result, activated T cells are attracted to B cells, which exert a "helper" role in lymphatic organs or in areas of inflammation. This observation provides a mechanistic explanation to previously reported experimental observations suggesting that B cells are required for T cell priming in vivo.

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