| Literature DB >> 25424910 |
Mary Poupot1, Frédéric Boissard, Delphine Betous, Laure Bardouillet, Séverine Fruchon, Fatima L'Faqihi-Olive, Frédéric Pont, Mourad Mekaouche, Sophie Ingoure, Hélène Sicard, Guy Dubreuilh, Jean-Jacques Fournié.
Abstract
Phosphoantigens (PAgs) activate Vγ9Vδ2 T lymphocytes, inducing their potent and rapid response in vitro and in vivo. However, humans and nonhuman primates that receive repeated injections of PAgs progressively lose their Vγ9Vδ2 T cell response to them. To elucidate the molecular mechanisms of this in vivo desensitization, we analyzed the transcriptome of circulating Vγ9Vδ2 T cells from macaques injected with PAg. We showed that three PAg injections induced the activation of the PPARα pathway in Vγ9Vδ2 T cells. Thus, we analyzed the in vitro response of Vγ9Vδ2 T cells stimulated with a PPARα agonist. We demonstrated that in vitro PPARα pathway activation led to the inhibition of the BrHPP-induced activation and proliferation of human Vγ9Vδ2 T cells. Since the PPARα pathway is involved in the antigen-selective desensitization of human Vγ9Vδ2 T cells, the use of PPARα inhibitors could enhance cancer immunotherapy based on Vγ9Vδ2 T cells.Entities:
Mesh:
Substances:
Year: 2014 PMID: 25424910 PMCID: PMC6275808 DOI: 10.2478/s11658-014-0218-0
Source DB: PubMed Journal: Cell Mol Biol Lett ISSN: 1425-8153 Impact factor: 5.787