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The CAR macrophage cells, a novel generation of chimeric antigen-based approach against solid tumors

Today, adoptive cell therapy has many successes in cancer therapy, and this subject is brilliant in using chimeric antigen receptor T cells. The CAR T cell therapy, with its FDA-approved drugs, could treat several types of hematological malignancies and thus be very attractive for treating solid can...

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Autores principales: Hadiloo, Kaveh, Taremi, Siavash, Heidari, Mahmood, Esmaeilzadeh, Abdolreza
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10685521/
https://www.ncbi.nlm.nih.gov/pubmed/38017494
http://dx.doi.org/10.1186/s40364-023-00537-x
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author Hadiloo, Kaveh
Taremi, Siavash
Heidari, Mahmood
Esmaeilzadeh, Abdolreza
author_facet Hadiloo, Kaveh
Taremi, Siavash
Heidari, Mahmood
Esmaeilzadeh, Abdolreza
author_sort Hadiloo, Kaveh
collection PubMed
description Today, adoptive cell therapy has many successes in cancer therapy, and this subject is brilliant in using chimeric antigen receptor T cells. The CAR T cell therapy, with its FDA-approved drugs, could treat several types of hematological malignancies and thus be very attractive for treating solid cancer. Unfortunately, the CAR T cell cannot be very functional in solid cancers due to its unique features. This treatment method has several harmful adverse effects that limit their applications, so novel treatments must use new cells like NK cells, NKT cells, and macrophage cells. Among these cells, the CAR macrophage cells, due to their brilliant innate features, are more attractive for solid tumor therapy and seem to be a better candidate for the prior treatment methods. The CAR macrophage cells have vital roles in the tumor microenvironment and, with their direct effect, can eliminate tumor cells efficiently. In addition, the CAR macrophage cells, due to being a part of the innate immune system, attended the tumor sites. With the high infiltration, their therapy modulations are more effective. This review investigates the last achievements in CAR-macrophage cells and the future of this immunotherapy treatment method. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40364-023-00537-x.
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spelling pubmed-106855212023-11-30 The CAR macrophage cells, a novel generation of chimeric antigen-based approach against solid tumors Hadiloo, Kaveh Taremi, Siavash Heidari, Mahmood Esmaeilzadeh, Abdolreza Biomark Res Review Today, adoptive cell therapy has many successes in cancer therapy, and this subject is brilliant in using chimeric antigen receptor T cells. The CAR T cell therapy, with its FDA-approved drugs, could treat several types of hematological malignancies and thus be very attractive for treating solid cancer. Unfortunately, the CAR T cell cannot be very functional in solid cancers due to its unique features. This treatment method has several harmful adverse effects that limit their applications, so novel treatments must use new cells like NK cells, NKT cells, and macrophage cells. Among these cells, the CAR macrophage cells, due to their brilliant innate features, are more attractive for solid tumor therapy and seem to be a better candidate for the prior treatment methods. The CAR macrophage cells have vital roles in the tumor microenvironment and, with their direct effect, can eliminate tumor cells efficiently. In addition, the CAR macrophage cells, due to being a part of the innate immune system, attended the tumor sites. With the high infiltration, their therapy modulations are more effective. This review investigates the last achievements in CAR-macrophage cells and the future of this immunotherapy treatment method. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40364-023-00537-x. BioMed Central 2023-11-28 /pmc/articles/PMC10685521/ /pubmed/38017494 http://dx.doi.org/10.1186/s40364-023-00537-x Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Review
Hadiloo, Kaveh
Taremi, Siavash
Heidari, Mahmood
Esmaeilzadeh, Abdolreza
The CAR macrophage cells, a novel generation of chimeric antigen-based approach against solid tumors
title The CAR macrophage cells, a novel generation of chimeric antigen-based approach against solid tumors
title_full The CAR macrophage cells, a novel generation of chimeric antigen-based approach against solid tumors
title_fullStr The CAR macrophage cells, a novel generation of chimeric antigen-based approach against solid tumors
title_full_unstemmed The CAR macrophage cells, a novel generation of chimeric antigen-based approach against solid tumors
title_short The CAR macrophage cells, a novel generation of chimeric antigen-based approach against solid tumors
title_sort car macrophage cells, a novel generation of chimeric antigen-based approach against solid tumors
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10685521/
https://www.ncbi.nlm.nih.gov/pubmed/38017494
http://dx.doi.org/10.1186/s40364-023-00537-x
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