CD5 on dendritic cells regulates CD4+ and CD8+ T cell activation and induction of immune responses
Year: 2019
Type: article
Abstract: The role of CD5 as a regulator of T cell signaling and tolerance is well recognized. Recent data show expression of CD5 on different subtypes of human dendritic cells, however its functional relevance in modulating DC mediated responses remains poorly understood. In this study, we show CD5 is expressed on CD11c+ DC from murine thymus, lymph node, spleen, skin and lung. Although the development of DC subpopulations in CD5-/- mice was normal, CD5-deficient DC produced significantly higher levels of IL-12 than wild type DC in response to LPS. CD5-/- DC, in comparison to CD5+/+ DC, enhanced the activation of CD4+ and CD8+ T cells in vitro and in vivo and induced significantly higher production of IL-2 and IFN-gamma by T cells. Consequently, CD5-/- DC were significantly more potent than wild type DC in the induction of anti-tumor immunity and contact hypersensitivity responses in mice. Restoration of CD5 expression in CD5-/- DC reduced IL-12 production and inhibited their capacity to stimulate T cells. Collectively, these data demonstrate that the specific expression of CD5 on DC inhibits the production of inflammatory cytokines and has a regulatory effect on their activity to stimulate T cells and induce immune responses. This study reveals a previously unrecognized regulatory role for CD5 on DC and provides novel insights into mechanisms for DC biology in immune responses.
Source: PLoS ONE
Language: English
Subfield: Immunology
Field: Immunology and Microbiology
Domain: Life Sciences
Open Access status: gold
Estimated APC paid: $1,595
Funders: National Multiple Sclerosis Society Michigan Chapter, Multiple Sclerosis Society, Consejo Nacional de Ciencia y Tecnología, National Institutes of Health, National Cancer Institute, National Institute of Allergy and Infectious Diseases, National Institute of Neurological Disorders and Stroke, National Institute of Environmental Health Sciences, National Institute of Arthritis and Musculoskeletal and Skin Diseases
Awards: The Role of CD5 In Dendritic Cell Mediated Immune Suppression, G230978185, G3301274224, UAB Research Center of Excellence in Arsenicals, Role of TGFBR3 in T-cell development and immune response, Chemoprevention of environmental UVB-induced skin cancer in immunosuppressed mice, G4946634508, Blocking Arsenicals-induced Cutaneous Injury, G684203367, Rheumatic Diseases Core Centers (P30), ALLERGIC CONTACT DERMATITIS: MECHANISMS OF ELICITATION, The Role of CD5 in B-Cell Development and Autoimmunity, G9000059695, G9000340949, Comprehensive Cancer Center Support Grant
OpenAlex ID: W2972112688
