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Impact of Immunotherapy on CD4 T Cell Phenotypes and Function in Cancer

Immunotherapy has become a standard treatment in many cancers and it is based on three main therapeutic axes: immune checkpoint blockade (ICB), vaccination and adoptive cell transfer (ACT). If originally these therapies mainly focused on exploiting CD8 T cells given their role in the direct eliminat...

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Detalles Bibliográficos
Autores principales: Saillard, Margaux, Cenerenti, Mara, Romero, Pedro, Jandus, Camilla
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8147771/
https://www.ncbi.nlm.nih.gov/pubmed/34064410
http://dx.doi.org/10.3390/vaccines9050454
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author Saillard, Margaux
Cenerenti, Mara
Romero, Pedro
Jandus, Camilla
author_facet Saillard, Margaux
Cenerenti, Mara
Romero, Pedro
Jandus, Camilla
author_sort Saillard, Margaux
collection PubMed
description Immunotherapy has become a standard treatment in many cancers and it is based on three main therapeutic axes: immune checkpoint blockade (ICB), vaccination and adoptive cell transfer (ACT). If originally these therapies mainly focused on exploiting CD8 T cells given their role in the direct elimination of tumor cells, increasing evidence highlights the crucial role CD4 T cells play in the antitumor immune response. Indeed, these cells can profoundly modulate the tumor microenvironment (TME) by secreting different types of cytokine or by directly eliminating cancer cells. In this review, we describe how different CD4 T cell subsets can contribute to tumor immune responses during immunotherapy and the novel high-throughput immune monitoring tools that are expected to facilitate the study of CD4 T cells, at antigen-specific and single cell level, thus accelerating bench-to-bed translational research in cancer.
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spelling pubmed-81477712021-05-26 Impact of Immunotherapy on CD4 T Cell Phenotypes and Function in Cancer Saillard, Margaux Cenerenti, Mara Romero, Pedro Jandus, Camilla Vaccines (Basel) Review Immunotherapy has become a standard treatment in many cancers and it is based on three main therapeutic axes: immune checkpoint blockade (ICB), vaccination and adoptive cell transfer (ACT). If originally these therapies mainly focused on exploiting CD8 T cells given their role in the direct elimination of tumor cells, increasing evidence highlights the crucial role CD4 T cells play in the antitumor immune response. Indeed, these cells can profoundly modulate the tumor microenvironment (TME) by secreting different types of cytokine or by directly eliminating cancer cells. In this review, we describe how different CD4 T cell subsets can contribute to tumor immune responses during immunotherapy and the novel high-throughput immune monitoring tools that are expected to facilitate the study of CD4 T cells, at antigen-specific and single cell level, thus accelerating bench-to-bed translational research in cancer. MDPI 2021-05-04 /pmc/articles/PMC8147771/ /pubmed/34064410 http://dx.doi.org/10.3390/vaccines9050454 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Saillard, Margaux
Cenerenti, Mara
Romero, Pedro
Jandus, Camilla
Impact of Immunotherapy on CD4 T Cell Phenotypes and Function in Cancer
title Impact of Immunotherapy on CD4 T Cell Phenotypes and Function in Cancer
title_full Impact of Immunotherapy on CD4 T Cell Phenotypes and Function in Cancer
title_fullStr Impact of Immunotherapy on CD4 T Cell Phenotypes and Function in Cancer
title_full_unstemmed Impact of Immunotherapy on CD4 T Cell Phenotypes and Function in Cancer
title_short Impact of Immunotherapy on CD4 T Cell Phenotypes and Function in Cancer
title_sort impact of immunotherapy on cd4 t cell phenotypes and function in cancer
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8147771/
https://www.ncbi.nlm.nih.gov/pubmed/34064410
http://dx.doi.org/10.3390/vaccines9050454
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