Redox Remodeling by Dendritic Cells Protects Antigen-Specific T Cells against Oxidative Stress

  • Martner A
  • Aurelius J
  • Rydström A
  • et al.
20Citations
Citations of this article
28Readers
Mendeley users who have this article in their library.
Get full text

Abstract

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.

Cite

CITATION STYLE

APA

Martner, A., Aurelius, J., Rydström, A., Hellstrand, K., & Thorén, F. B. (2011). Redox Remodeling by Dendritic Cells Protects Antigen-Specific T Cells against Oxidative Stress. The Journal of Immunology, 187(12), 6243–6248. https://doi.org/10.4049/jimmunol.1102138

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free