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The prospect of genetically engineering natural killer cells for cancer immunotherapy

The use of natural killer (NK) cells in cancer immunotherapy demonstrates promising potential, yet its efficacy is often limited due to the loss of tumor-killing capacity and lack of specificity in vivo. Here, we review current approaches to confer enhanced tumor-killing capacity and specificity by...

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Detalles Bibliográficos
Autores principales: Poon, Angie Yu Ching, Sugimura, Ryohichi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Company of Biologists Ltd 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9729658/
https://www.ncbi.nlm.nih.gov/pubmed/36445164
http://dx.doi.org/10.1242/bio.059396
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author Poon, Angie Yu Ching
Sugimura, Ryohichi
author_facet Poon, Angie Yu Ching
Sugimura, Ryohichi
author_sort Poon, Angie Yu Ching
collection PubMed
description The use of natural killer (NK) cells in cancer immunotherapy demonstrates promising potential, yet its efficacy is often limited due to the loss of tumor-killing capacity and lack of specificity in vivo. Here, we review current approaches to confer enhanced tumor-killing capacity and specificity by genetic engineering. Increasing sensitivity to cytokines and protecting NK cells from the immune checkpoint endowed sustainability of NK cells in the tumor microenvironment. Transducing chimeric antigen receptor (CAR) in NK cells successfully targeted both hematologic and solid tumors in preclinical models. The use of human pluripotent stem cells as an expandable and genetically amenable platform offers a stable source of engineered NK cells for cancer immunotherapy. We highlight that CAR-NK cells from human pluripotent stem cells are a promising approach for cancer immunotherapy.
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spelling pubmed-97296582022-12-08 The prospect of genetically engineering natural killer cells for cancer immunotherapy Poon, Angie Yu Ching Sugimura, Ryohichi Biol Open Review The use of natural killer (NK) cells in cancer immunotherapy demonstrates promising potential, yet its efficacy is often limited due to the loss of tumor-killing capacity and lack of specificity in vivo. Here, we review current approaches to confer enhanced tumor-killing capacity and specificity by genetic engineering. Increasing sensitivity to cytokines and protecting NK cells from the immune checkpoint endowed sustainability of NK cells in the tumor microenvironment. Transducing chimeric antigen receptor (CAR) in NK cells successfully targeted both hematologic and solid tumors in preclinical models. The use of human pluripotent stem cells as an expandable and genetically amenable platform offers a stable source of engineered NK cells for cancer immunotherapy. We highlight that CAR-NK cells from human pluripotent stem cells are a promising approach for cancer immunotherapy. The Company of Biologists Ltd 2022-11-29 /pmc/articles/PMC9729658/ /pubmed/36445164 http://dx.doi.org/10.1242/bio.059396 Text en © 2022. Published by The Company of Biologists Ltd https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.
spellingShingle Review
Poon, Angie Yu Ching
Sugimura, Ryohichi
The prospect of genetically engineering natural killer cells for cancer immunotherapy
title The prospect of genetically engineering natural killer cells for cancer immunotherapy
title_full The prospect of genetically engineering natural killer cells for cancer immunotherapy
title_fullStr The prospect of genetically engineering natural killer cells for cancer immunotherapy
title_full_unstemmed The prospect of genetically engineering natural killer cells for cancer immunotherapy
title_short The prospect of genetically engineering natural killer cells for cancer immunotherapy
title_sort prospect of genetically engineering natural killer cells for cancer immunotherapy
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9729658/
https://www.ncbi.nlm.nih.gov/pubmed/36445164
http://dx.doi.org/10.1242/bio.059396
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