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Polymer- and lipid-based gene delivery technology for CAR T cell therapy.

Authors :
Pinto IS
Cordeiro RA
Faneca H
Source :
Journal of controlled release : official journal of the Controlled Release Society [J Control Release] 2023 Jan; Vol. 353, pp. 196-215. Date of Electronic Publication: 2022 Nov 25.
Publication Year :
2023

Abstract

Chimeric antigen receptor T cell (CAR T cell) therapy is a revolutionary approach approved by the FDA and EMA to treat B cell malignancies and multiple myeloma. The production of these T cells has been done through viral vectors, which come with safety concerns, high cost and production challenges, and more recently also through electroporation, which can be extremely cytotoxic. In this context, nanosystems can constitute an alternative to overcome the challenges associated with current methods, resulting in a safe and cost-effective platform. However, the barriers associated with T cells transfection show that the design and engineering of novel approaches in this field are highly imperative. Here, we present an overview from CAR constitution to transfection technologies used in T cells, highlighting the lipid- and polymer-based nanoparticles as a potential delivery platform. Specifically, we provide examples, strengths and weaknesses of nanosystem formulations, and advances in nanoparticle design to improve transfection of T cells. This review will guide the researchers in the design and development of novel nanosystems for next-generation CAR T therapeutics.<br />Competing Interests: Declaration of Competing Interest Henrique Faneca reports a relationship with Lupagen, Inc. that includes: funding grants. Rosemeyre Cordeiro reports a relationship with Gilead Sciences, Lda. that includes: funding grants.<br /> (Copyright © 2022 The Authors. Published by Elsevier B.V. All rights reserved.)

Details

Language :
English
ISSN :
1873-4995
Volume :
353
Database :
MEDLINE
Journal :
Journal of controlled release : official journal of the Controlled Release Society
Publication Type :
Academic Journal
Accession number :
36423871
Full Text :
https://doi.org/10.1016/j.jconrel.2022.11.038