CTLA-4 and PD-1 Control of T-Cell Motility and Migration: Implications for Tumor Immunotherapy

CTLA-4 is a co-receptor on T-cells that controls peripheral tolerance and the development of autoimmunity. Immune check-point blockade (ICB) uses monoclonal antibodies (MAbs) to block the binding of inhibitory receptors (IRs) to their natural ligands. A humanized antibody to CTLA-4 was first approve...

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Main Authors: Monika C. Brunner-Weinzierl, Christopher E. Rudd
Format: Article
Language:English
Published: Frontiers Media S.A. 2018-11-01
Series:Frontiers in Immunology
Subjects:
Online Access:https://www.frontiersin.org/article/10.3389/fimmu.2018.02737/full
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spelling doaj-3237a98799ac4c94aa36b3269e66902c2020-11-25T02:24:36ZengFrontiers Media S.A.Frontiers in Immunology1664-32242018-11-01910.3389/fimmu.2018.02737410152CTLA-4 and PD-1 Control of T-Cell Motility and Migration: Implications for Tumor ImmunotherapyMonika C. Brunner-Weinzierl0Christopher E. Rudd1Christopher E. Rudd2Department of Experimental Pediatrics, University Hospital, Health Campus Immunology, Infectiology and Inflammation, Otto-von-Guericke-University, Magdeburg, GermanyResearch Center-Maisonneuve-Rosemont Hospital (CRHMR), Montreal, QC, CanadaDépartement de Medicine, Université de Montréal, Montreal, QC, CanadaCTLA-4 is a co-receptor on T-cells that controls peripheral tolerance and the development of autoimmunity. Immune check-point blockade (ICB) uses monoclonal antibodies (MAbs) to block the binding of inhibitory receptors (IRs) to their natural ligands. A humanized antibody to CTLA-4 was first approved clinically followed by the use of antibody blockade against PD-1 and its ligand PD-L1. Effective anti-tumor immunity requires the activation of tumor-specific effector T-cells, the blockade of regulatory cells and the migration of T-cells into the tumor. Here, we review data implicating CTLA-4 and PD-1 in the motility of T-cells with a specific reference to the potential exploitation of these pathways for more effective tumor infiltration and eradication.https://www.frontiersin.org/article/10.3389/fimmu.2018.02737/fullCTLA4check-point blockadecancerT-cellmotilitymigration
collection DOAJ
language English
format Article
sources DOAJ
author Monika C. Brunner-Weinzierl
Christopher E. Rudd
Christopher E. Rudd
spellingShingle Monika C. Brunner-Weinzierl
Christopher E. Rudd
Christopher E. Rudd
CTLA-4 and PD-1 Control of T-Cell Motility and Migration: Implications for Tumor Immunotherapy
Frontiers in Immunology
CTLA4
check-point blockade
cancer
T-cell
motility
migration
author_facet Monika C. Brunner-Weinzierl
Christopher E. Rudd
Christopher E. Rudd
author_sort Monika C. Brunner-Weinzierl
title CTLA-4 and PD-1 Control of T-Cell Motility and Migration: Implications for Tumor Immunotherapy
title_short CTLA-4 and PD-1 Control of T-Cell Motility and Migration: Implications for Tumor Immunotherapy
title_full CTLA-4 and PD-1 Control of T-Cell Motility and Migration: Implications for Tumor Immunotherapy
title_fullStr CTLA-4 and PD-1 Control of T-Cell Motility and Migration: Implications for Tumor Immunotherapy
title_full_unstemmed CTLA-4 and PD-1 Control of T-Cell Motility and Migration: Implications for Tumor Immunotherapy
title_sort ctla-4 and pd-1 control of t-cell motility and migration: implications for tumor immunotherapy
publisher Frontiers Media S.A.
series Frontiers in Immunology
issn 1664-3224
publishDate 2018-11-01
description CTLA-4 is a co-receptor on T-cells that controls peripheral tolerance and the development of autoimmunity. Immune check-point blockade (ICB) uses monoclonal antibodies (MAbs) to block the binding of inhibitory receptors (IRs) to their natural ligands. A humanized antibody to CTLA-4 was first approved clinically followed by the use of antibody blockade against PD-1 and its ligand PD-L1. Effective anti-tumor immunity requires the activation of tumor-specific effector T-cells, the blockade of regulatory cells and the migration of T-cells into the tumor. Here, we review data implicating CTLA-4 and PD-1 in the motility of T-cells with a specific reference to the potential exploitation of these pathways for more effective tumor infiltration and eradication.
topic CTLA4
check-point blockade
cancer
T-cell
motility
migration
url https://www.frontiersin.org/article/10.3389/fimmu.2018.02737/full
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