Toroidal-spiral particles as a CAR-T cell delivery device for solid tumor immunotherapy.
Adoptive cellular therapy
Biodegradable particle
Immunotherapy
In vivo cell incubator
Programmable release
Self-assembly
Journal
Journal of controlled release : official journal of the Controlled Release Society
ISSN: 1873-4995
Titre abrégé: J Control Release
Pays: Netherlands
ID NLM: 8607908
Informations de publication
Date de publication:
10 2023
10 2023
Historique:
received:
16
09
2022
revised:
29
08
2023
accepted:
02
09
2023
medline:
4
3
2024
pubmed:
7
9
2023
entrez:
6
9
2023
Statut:
ppublish
Résumé
Chimeric antigen receptor (CAR) T cell therapy has resulted in positive effects on patients with hematologic malignancy but shows limited efficacy in solid tumor treatments due to insufficient trafficking and tumor infiltration, intensive CAR-T-related toxicities, and antigen escape. In this work, we developed and investigated a biodegradable and biocompatible polymeric toroidal-spiral particle (TSP) as a in vivo cell incubator and delivery device that can be implanted near tumor through a minimally invasive procedure or injected near or into solid tumors by using a biopsy needle. The main matrix structure of the millimeter-sized TSP is made from crosslinking of gelatin methacrylamine (GelMA) and poly (ethylene glycol) diacrylate (PEGDA) with a tunable degradation rate from a few days to months, providing appropriate mechanical properties and sustained release of co-encapsulated drugs and/or stimulation compounds. The toroidal-spiral layer of the particles, presenting an internal void volume for high-capacity cell loading and flexibility of co-encapsulating small and large molecular compounds with individually manipulated release schedules, is filled with collagen and suspended T cells. The TSPs promote cell proliferation, activation, and migration in the tumor micro-environment in a prolonged and sustained manner. In this study, the efficacy of mesothelin (MSLN) CAR-T cells released from the TSPs was tested in preclinical mouse tumor models. Compared to systemic and intratumoral injection, peritumoral delivery of MSLN CAR-T cells using the TSPs resulted in a superior antitumor effect. The TSPs made of FDA approved materials as an in vivo reactor may provide an option for efficiently local delivery of CAR-T cells to solid tumors for higher efficacy and lower toxicity, with a minimally invasive administration procedure.
Identifiants
pubmed: 37673306
pii: S0168-3659(23)00590-4
doi: 10.1016/j.jconrel.2023.09.005
pmc: PMC10947521
mid: NIHMS1971451
pii:
doi:
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
620-630Subventions
Organisme : NCI NIH HHS
ID : P30 CA060553
Pays : United States
Organisme : NCI NIH HHS
ID : R01 CA222963
Pays : United States
Organisme : NCI NIH HHS
ID : R01 CA250101
Pays : United States
Organisme : NCI NIH HHS
ID : R01 CA258857
Pays : United States
Informations de copyright
Copyright © 2023 Elsevier B.V. All rights reserved.
Déclaration de conflit d'intérêts
Declaration of Competing Interest A US patent has been filed by the University of Illinois Chicago, Application number: 63/073,382 filed on Aug. 29, 2021. In situ Cell Bioreactor and Delivery System and Methods of Using the Same. Ying Liu.
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