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Engineering enhanced chimeric antigen receptor-T cell therapy for solid tumors

The early clinical success and subsequent US Food and Drug Administration approval of chimeric antigen receptor (CAR)-T cell therapy for leukemia and lymphoma affirm that engineered T cells can be a powerful treatment for hematologic malignancies. Yet this success has not been replicated in solid tu...

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Detalles Bibliográficos
Autores principales: Neeser, A., Ramasubramanian, R., Wang, C., Ma, L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10362352/
https://www.ncbi.nlm.nih.gov/pubmed/37483659
http://dx.doi.org/10.1016/j.iotech.2023.100385
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author Neeser, A.
Ramasubramanian, R.
Wang, C.
Ma, L.
author_facet Neeser, A.
Ramasubramanian, R.
Wang, C.
Ma, L.
author_sort Neeser, A.
collection PubMed
description The early clinical success and subsequent US Food and Drug Administration approval of chimeric antigen receptor (CAR)-T cell therapy for leukemia and lymphoma affirm that engineered T cells can be a powerful treatment for hematologic malignancies. Yet this success has not been replicated in solid tumors. Numerous challenges emerged from clinical experience and well-controlled preclinical animal models must be met to enable safe and efficacious CAR-T cell therapy in solid tumors. Here, we review recent advances in bioengineering strategies developed to enhance CAR-T cell therapy in solid tumors, focusing on targeted single-gene perturbation, genetic circuits design, cytokine engineering, and interactive biomaterials. These bioengineering approaches present a unique set of tools that synergize with CAR-T cells to overcome obstacles in solid tumors and achieve robust and long-lasting therapeutic efficacy.
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spelling pubmed-103623522023-07-23 Engineering enhanced chimeric antigen receptor-T cell therapy for solid tumors Neeser, A. Ramasubramanian, R. Wang, C. Ma, L. Immunooncol Technol Review The early clinical success and subsequent US Food and Drug Administration approval of chimeric antigen receptor (CAR)-T cell therapy for leukemia and lymphoma affirm that engineered T cells can be a powerful treatment for hematologic malignancies. Yet this success has not been replicated in solid tumors. Numerous challenges emerged from clinical experience and well-controlled preclinical animal models must be met to enable safe and efficacious CAR-T cell therapy in solid tumors. Here, we review recent advances in bioengineering strategies developed to enhance CAR-T cell therapy in solid tumors, focusing on targeted single-gene perturbation, genetic circuits design, cytokine engineering, and interactive biomaterials. These bioengineering approaches present a unique set of tools that synergize with CAR-T cells to overcome obstacles in solid tumors and achieve robust and long-lasting therapeutic efficacy. Elsevier 2023-05-24 /pmc/articles/PMC10362352/ /pubmed/37483659 http://dx.doi.org/10.1016/j.iotech.2023.100385 Text en © 2023 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Review
Neeser, A.
Ramasubramanian, R.
Wang, C.
Ma, L.
Engineering enhanced chimeric antigen receptor-T cell therapy for solid tumors
title Engineering enhanced chimeric antigen receptor-T cell therapy for solid tumors
title_full Engineering enhanced chimeric antigen receptor-T cell therapy for solid tumors
title_fullStr Engineering enhanced chimeric antigen receptor-T cell therapy for solid tumors
title_full_unstemmed Engineering enhanced chimeric antigen receptor-T cell therapy for solid tumors
title_short Engineering enhanced chimeric antigen receptor-T cell therapy for solid tumors
title_sort engineering enhanced chimeric antigen receptor-t cell therapy for solid tumors
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10362352/
https://www.ncbi.nlm.nih.gov/pubmed/37483659
http://dx.doi.org/10.1016/j.iotech.2023.100385
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