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
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

620-630

Subventions

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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Auteurs

Hui Tang (H)

Feinberg School of Medicine, Northwestern University, Chicago, IL, United States.

Maryam Zaroudi (M)

Department of Chemical Engineering, University of Illinois at Chicago, Chicago, IL, United States.

Yuli Zhu (Y)

Department of Chemical Engineering, University of Illinois at Chicago, Chicago, IL, United States.

Alex Cheng (A)

Department of Chemical Engineering, University of Illinois at Chicago, Chicago, IL, United States.

Lei Qin (L)

Feinberg School of Medicine, Northwestern University, Chicago, IL, United States.

Bin Zhang (B)

Feinberg School of Medicine, Northwestern University, Chicago, IL, United States. Electronic address: bin.zhang@northwestern.edu.

Ying Liu (Y)

Department of Chemical Engineering, University of Illinois at Chicago, Chicago, IL, United States; Department of Biomedical Engineering, University of Illinois at Chicago, Chicago, IL, United States; Department of Pharmaceutical Sciences, University of Illinois at Chicago, Chicago, IL, United States. Electronic address: liuying@uic.edu.

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Classifications MeSH