Adenosine and cAMP signalling skew human dendritic cell differentiation towards a tolerogenic phenotype with defective CD8+ T-cell priming capacity

Challier, John, Bruniquel, Denis, Sewell, Andrew K. ORCID: https://orcid.org/0000-0003-3194-3135 and Laugel, Bruno 2013. Adenosine and cAMP signalling skew human dendritic cell differentiation towards a tolerogenic phenotype with defective CD8+ T-cell priming capacity. Immunology 138 (4) , pp. 402-410. 10.1111/imm.12053

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Abstract

Multiple endogenous mechanisms that regulate immune and inflammatory processes contribute to the maintenance of peripheral tolerance and prevent chronic inflammation in mammals. Yet pathogens and tumours are able to exploit these homeostatic pathways to foster immunosuppressive microenvironments and evade immune surveillance. The release of adenosine in the extracellular space contributes to these phenomena by exerting a broad range of immunomodulatory effects. Here we document the influence of adenosine receptor triggering on human dendritic cell differentiation and functions. We show that the expression of several immunomodulatory proteins and myeloid/monocytic lineage markers was affected by adenosine receptors and the cAMP pathway. These changes were reminiscent of the phenotype associated with tolerogenic dendritic cells and, functionally, translated into a defective capacity to prime CD8+ T-cells with a common tumour antigen in vitro. These results establish a novel mechanism by which adenosine hampers CD8+ T-cell immunity via dendritic cells that may contribute to peripheral tolerance as well as to the establishment of immunosuppressive microenvironments relevant to tumour biology.

Item Type:	Article
Date Type:	Publication
Status:	Published
Schools:	Medicine
Subjects:	Q Science > QR Microbiology > QR180 Immunology R Medicine > R Medicine (General)
Uncontrolled Keywords:	Adenosine; Biological Markers; CD8-Positive T-Lymphocytes; Cell Differentiation; Cells, Cultured; Cyclic AMP; Cytokines; Dendritic Cells; Gene Expression; Humans; Immunologic Factors; Monocytes; Peripheral Tolerance; Phenotype; Receptors, Purinergic P1; Signal Transduction
Publisher:	Wiley Blackwell
ISSN:	0019-2805
Date of Acceptance:	14 December 2012
Last Modified:	06 May 2023 02:23
URI:	https://orca.cardiff.ac.uk/id/eprint/80110

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