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Redox Remodeling by Dendritic Cells Protects Antigen-Specific T Cells against Oxidative Stress
Author(s) -
Anna Martner,
Johan Aurelius,
Anna Rydström,
Kristoffer Hellstrand,
Fredrik B. Thorén
Publication year - 2011
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.1102138
Subject(s) - microbiology and biotechnology , reactive oxygen species , oxidative stress , antigen presentation , apoptosis , chemistry , antigen presenting cell , extracellular , dendritic cell , t cell , cytotoxic t cell , cell , cross presentation , biology , immune system , immunology , biochemistry , in vitro
Microorganisms and microbial products induce the release of reactive oxygen species (ROS) from monocytes and other myeloid cells, which may trigger dysfunction and apoptosis of adjacent lymphocytes. Therefore, T cell-mediated immunity is likely to comprise mechanisms of T cell protection against ROS-inflicted toxicity. The present study aimed to clarify the dynamics of reduced sulfhydryl groups (thiols) in human T cells after presentation of viral and bacterial Ags by dendritic cells (DCs) or B cells. DCs, but not B cells, efficiently triggered intra- and extracellular thiol expression in T cells with corresponding Ag specificity. After interaction with DCs, the Ag-specific T cells acquired the capacity to neutralize exogenous oxygen radicals and resisted ROS-induced apoptosis. Our results imply that DCs provide Ag-specific T cells with antioxidative thiols during Ag presentation, which suggests a novel aspect of DC/T cell cross-talk of relevance to the maintenance of specific immunity in inflamed or infected tissue.

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