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CAR-NK Cells in the Treatment of Solid Tumors

CAR-T (chimeric antigen receptor T) cells have emerged as a milestone in the treatment of patients with refractory B-cell neoplasms. However, despite having unprecedented efficacy against hematological malignancies, the treatment is far from flawless. Its greatest drawbacks arise from a challenging...

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Detalles Bibliográficos
Autores principales: Wrona, Ewa, Borowiec, Maciej, Potemski, Piotr
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8197981/
https://www.ncbi.nlm.nih.gov/pubmed/34072732
http://dx.doi.org/10.3390/ijms22115899
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author Wrona, Ewa
Borowiec, Maciej
Potemski, Piotr
author_facet Wrona, Ewa
Borowiec, Maciej
Potemski, Piotr
author_sort Wrona, Ewa
collection PubMed
description CAR-T (chimeric antigen receptor T) cells have emerged as a milestone in the treatment of patients with refractory B-cell neoplasms. However, despite having unprecedented efficacy against hematological malignancies, the treatment is far from flawless. Its greatest drawbacks arise from a challenging and expensive production process, strict patient eligibility criteria and serious toxicity profile. One possible solution, supported by robust research, is the replacement of T lymphocytes with NK cells for CAR expression. NK cells seem to be an attractive vehicle for CAR expression as they can be derived from multiple sources and safely infused regardless of donor–patient matching, which greatly reduces the cost of the treatment. CAR-NK cells are known to be effective against hematological malignancies, and a growing number of preclinical findings indicate that they have activity against non-hematological neoplasms. Here, we present a thorough overview of the current state of knowledge regarding the use of CAR-NK cells in treating various solid tumors.
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spelling pubmed-81979812021-06-14 CAR-NK Cells in the Treatment of Solid Tumors Wrona, Ewa Borowiec, Maciej Potemski, Piotr Int J Mol Sci Review CAR-T (chimeric antigen receptor T) cells have emerged as a milestone in the treatment of patients with refractory B-cell neoplasms. However, despite having unprecedented efficacy against hematological malignancies, the treatment is far from flawless. Its greatest drawbacks arise from a challenging and expensive production process, strict patient eligibility criteria and serious toxicity profile. One possible solution, supported by robust research, is the replacement of T lymphocytes with NK cells for CAR expression. NK cells seem to be an attractive vehicle for CAR expression as they can be derived from multiple sources and safely infused regardless of donor–patient matching, which greatly reduces the cost of the treatment. CAR-NK cells are known to be effective against hematological malignancies, and a growing number of preclinical findings indicate that they have activity against non-hematological neoplasms. Here, we present a thorough overview of the current state of knowledge regarding the use of CAR-NK cells in treating various solid tumors. MDPI 2021-05-31 /pmc/articles/PMC8197981/ /pubmed/34072732 http://dx.doi.org/10.3390/ijms22115899 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
Wrona, Ewa
Borowiec, Maciej
Potemski, Piotr
CAR-NK Cells in the Treatment of Solid Tumors
title CAR-NK Cells in the Treatment of Solid Tumors
title_full CAR-NK Cells in the Treatment of Solid Tumors
title_fullStr CAR-NK Cells in the Treatment of Solid Tumors
title_full_unstemmed CAR-NK Cells in the Treatment of Solid Tumors
title_short CAR-NK Cells in the Treatment of Solid Tumors
title_sort car-nk cells in the treatment of solid tumors
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8197981/
https://www.ncbi.nlm.nih.gov/pubmed/34072732
http://dx.doi.org/10.3390/ijms22115899
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