TY - JOUR
T1 - Harnessing γδ T cells in anticancer immunotherapy
AU - Hannani, Dalil
AU - Ma, Yuting
AU - Yamazaki, Takahiro
AU - Déchanet-Merville, Julie
AU - Kroemer, Guido
AU - Zitvogel, Laurence
N1 - Funding Information:
D.H is supported by Association pour la Recherche sur le Cancer. Y.M is supported by the China Scholarship Council. T.Y is supported by INSERM. JDM is supported by Fondation pour la Recherche Médicale (Equipe labellisée), Ligue Contre le Cancer, Association pour la Recherche contre le Cancer and INCA. GK is supported by Ligue Nationale contre le Cancer (Equipes labellisée), Agence Nationale pour la Recherche, the AXA Chair for Longevity Research, European Commission (Apo-Sys, ArtForce, ChemoRes, ApopTrain), Fondation Bettencourt-Schueller, Fondation pour la Recherche Médicale, Institut National du Cancer and Cancéropôle Ile-de-France. LZ is supported by Ligue contre le Cancer (équipe labellisée), Fondation pour la Recherche Médicale, INFLACARE EU grant 2008, INCa and Fondation de France (2009-2011).
PY - 2012/5/1
Y1 - 2012/5/1
N2 - γδ T lymphocytes are involved in the stress response to injured epithelia and in tissue homeostasis by limiting the dissemination of malignant or infected cells and by regulating the nature of the subsequent adaptive immune response. γδ T cells have potent MHC-unrestricted cytotoxicity, a high potential for cytokine release and broad-spectrum recognition of cancer cells, and as such, are attractive effectors for cancer immunotherapy. Current expectations are going beyond ex vivo manipulation of the Vγ9Vδ2 T subset, and target novel γδ T cell subsets, properties or receptors, to harness these unconventional T lymphocytes against cancer. This Opinion article discusses novel aspects of γδ T cell function during the course of anticancer therapies, as well as new avenues for their clinical implementation.
AB - γδ T lymphocytes are involved in the stress response to injured epithelia and in tissue homeostasis by limiting the dissemination of malignant or infected cells and by regulating the nature of the subsequent adaptive immune response. γδ T cells have potent MHC-unrestricted cytotoxicity, a high potential for cytokine release and broad-spectrum recognition of cancer cells, and as such, are attractive effectors for cancer immunotherapy. Current expectations are going beyond ex vivo manipulation of the Vγ9Vδ2 T subset, and target novel γδ T cell subsets, properties or receptors, to harness these unconventional T lymphocytes against cancer. This Opinion article discusses novel aspects of γδ T cell function during the course of anticancer therapies, as well as new avenues for their clinical implementation.
KW - Cancer
KW - Immunotherapy
KW - γδ T cells
UR - http://www.scopus.com/inward/record.url?scp=84862812850&partnerID=8YFLogxK
U2 - 10.1016/j.it.2012.01.006
DO - 10.1016/j.it.2012.01.006
M3 - Review article
C2 - 22364810
AN - SCOPUS:84862812850
SN - 1471-4906
VL - 33
SP - 199
EP - 206
JO - Trends in Immunology
JF - Trends in Immunology
IS - 5
ER -