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CXCR6 expressing T cells: Functions and role in the control of tumors

CXCR6 is a receptor for the chemokine CXCL16, which exists as a membrane or soluble form. CXCR6 is a marker for resident memory T (T(RM)) cells that plays a role in immunosurveillance through their interaction with epithelial cells. The interaction of CXCR6 with CXCL16 expressed at the membrane of c...

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Autores principales: Mabrouk, Nesrine, Tran, Thi, Sam, Ikuan, Pourmir, Ivan, Gruel, Nadège, Granier, Clémence, Pineau, Joséphine, Gey, Alain, Kobold, Sebastian, Fabre, Elizabeth, Tartour, Eric
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9597613/
https://www.ncbi.nlm.nih.gov/pubmed/36311728
http://dx.doi.org/10.3389/fimmu.2022.1022136
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author Mabrouk, Nesrine
Tran, Thi
Sam, Ikuan
Pourmir, Ivan
Gruel, Nadège
Granier, Clémence
Pineau, Joséphine
Gey, Alain
Kobold, Sebastian
Fabre, Elizabeth
Tartour, Eric
author_facet Mabrouk, Nesrine
Tran, Thi
Sam, Ikuan
Pourmir, Ivan
Gruel, Nadège
Granier, Clémence
Pineau, Joséphine
Gey, Alain
Kobold, Sebastian
Fabre, Elizabeth
Tartour, Eric
author_sort Mabrouk, Nesrine
collection PubMed
description CXCR6 is a receptor for the chemokine CXCL16, which exists as a membrane or soluble form. CXCR6 is a marker for resident memory T (T(RM)) cells that plays a role in immunosurveillance through their interaction with epithelial cells. The interaction of CXCR6 with CXCL16 expressed at the membrane of certain subpopulations of intratumor dendritic cells (DC) called DC3, ideally positions these CXCR6(+) T cells to receive a proliferation signal from IL-15 also presented by DC3. Mice deficient in cxcr6 or blocking the interaction of CXCR6 with its ligand, experience a poorer control of tumor proliferation by CD8(+) T cells, but also by NKT cells especially in the liver. Intranasal vaccination induces CXCL16 production in the lungs and is associated with infiltration by T(RM) expressing CXCR6, which are then required for the efficacy of anti-tumor vaccination. Therapeutically, the addition of CXCR6 to specific CAR-T cells enhances their intratumoral accumulation and prolongs survival in animal models of pancreatic, ovarian and lung cancer. Finally, CXCR6 is part of immunological signatures that predict response to immunotherapy based on anti-PD-(L)1 in various cancers. In contrast, a protumoral role of CXCR6(+)T cells has also been reported mainly in Non-alcoholic steatohepatitis (NASH) due to a non-antigen specific mechanism. The targeting and amplification of antigen-specific T(RM) expressing CXCR6 and its potential use as a biomarker of response to immunotherapy opens new perspectives in cancer treatment.
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spelling pubmed-95976132022-10-27 CXCR6 expressing T cells: Functions and role in the control of tumors Mabrouk, Nesrine Tran, Thi Sam, Ikuan Pourmir, Ivan Gruel, Nadège Granier, Clémence Pineau, Joséphine Gey, Alain Kobold, Sebastian Fabre, Elizabeth Tartour, Eric Front Immunol Immunology CXCR6 is a receptor for the chemokine CXCL16, which exists as a membrane or soluble form. CXCR6 is a marker for resident memory T (T(RM)) cells that plays a role in immunosurveillance through their interaction with epithelial cells. The interaction of CXCR6 with CXCL16 expressed at the membrane of certain subpopulations of intratumor dendritic cells (DC) called DC3, ideally positions these CXCR6(+) T cells to receive a proliferation signal from IL-15 also presented by DC3. Mice deficient in cxcr6 or blocking the interaction of CXCR6 with its ligand, experience a poorer control of tumor proliferation by CD8(+) T cells, but also by NKT cells especially in the liver. Intranasal vaccination induces CXCL16 production in the lungs and is associated with infiltration by T(RM) expressing CXCR6, which are then required for the efficacy of anti-tumor vaccination. Therapeutically, the addition of CXCR6 to specific CAR-T cells enhances their intratumoral accumulation and prolongs survival in animal models of pancreatic, ovarian and lung cancer. Finally, CXCR6 is part of immunological signatures that predict response to immunotherapy based on anti-PD-(L)1 in various cancers. In contrast, a protumoral role of CXCR6(+)T cells has also been reported mainly in Non-alcoholic steatohepatitis (NASH) due to a non-antigen specific mechanism. The targeting and amplification of antigen-specific T(RM) expressing CXCR6 and its potential use as a biomarker of response to immunotherapy opens new perspectives in cancer treatment. Frontiers Media S.A. 2022-10-12 /pmc/articles/PMC9597613/ /pubmed/36311728 http://dx.doi.org/10.3389/fimmu.2022.1022136 Text en Copyright © 2022 Mabrouk, Tran, Sam, Pourmir, Gruel, Granier, Pineau, Gey, Kobold, Fabre and Tartour https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Mabrouk, Nesrine
Tran, Thi
Sam, Ikuan
Pourmir, Ivan
Gruel, Nadège
Granier, Clémence
Pineau, Joséphine
Gey, Alain
Kobold, Sebastian
Fabre, Elizabeth
Tartour, Eric
CXCR6 expressing T cells: Functions and role in the control of tumors
title CXCR6 expressing T cells: Functions and role in the control of tumors
title_full CXCR6 expressing T cells: Functions and role in the control of tumors
title_fullStr CXCR6 expressing T cells: Functions and role in the control of tumors
title_full_unstemmed CXCR6 expressing T cells: Functions and role in the control of tumors
title_short CXCR6 expressing T cells: Functions and role in the control of tumors
title_sort cxcr6 expressing t cells: functions and role in the control of tumors
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9597613/
https://www.ncbi.nlm.nih.gov/pubmed/36311728
http://dx.doi.org/10.3389/fimmu.2022.1022136
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