Dextran-based T-cell expansion nanoparticles for manufacturing CAR T cells with augmented efficacy

Adoptive T cell therapy using chimeric antigen receptor (CAR) engineered T cells is currently being explored in multiple cancer types beyond leukemia/lymphoma. A key step in CAR-T cell manufacturing is the activation and expansion of T cells, which facilitates viral transduction, however, may hamper T cell fitness and reduce in vivo persistence. "T-Expand" is developed for T cell activation and expansion, comprising dextran-based nanoparticles conjugated with anti-CD3 and anti-CD28 antibodies. The nanoparticles trigger robust polyclonal expansion of human T cells with efficiency in the range of commercial microbeads (Dynabeads™). Engineered in the presence of T-Expand, CD19 CAR T cells display enhanced proliferative capacity, cytotoxicity and persistence in vitro, and furthermore, exhibit potent anti-lymphoma activity in mouse models, resulting in complete tumor clearance at one fourth of the CAR T cell dose. Importantly, T-Expand is biocompatible with no observed toxicity, circumventing removal steps after T cell expansion compared to Dynabeads<sup>TM</sup>. As a biocompatible T cell expansion platform, T-Expand simplifies the manufacturing process while enhancing T cell persistence and functionality, and thereby holds promise for increasing clinical efficacy of CAR T cell therapy.

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Publication Details

Journal
Nature Communications
Published
2026-01-20
DOI
https://doi.org/10.1038/s41467-025-67868-1
Primary Topic
CAR-T cell therapy research
Type
article
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article

Dextran-based T-cell expansion nanoparticles for manufacturing CAR T cells with augmented efficacy

Keerthana Ramanathan, Sine Reker Hadrup, Rasmus U. W. Friis, Hólmfridur R. Halldórsdóttir et al.
Nature Communications
CAR-T cell therapy research
article

Dextran-based T-cell expansion nanoparticles for manufacturing CAR T cells with augmented efficacy

Keerthana Ramanathan, Sine Reker Hadrup, Rasmus U. W. Friis, Hólmfridur R. Halldórsdóttir, Islam Seder, Klaus Qvortrup, Hanxi Li, Hinrich Abken, Mikkel Rasmus Hansen, Maria Ormhøj, Yi Sun, Kamilla Kjærgaard Munk, Carlos Rodriguez-Pardo, Peter M. H. Heegaard, Tao Zheng
article en

Abstract

Adoptive T cell therapy using chimeric antigen receptor (CAR) engineered T cells is currently being explored in multiple cancer types beyond leukemia/lymphoma. A key step in CAR-T cell manufacturing is the activation and expansion of T cells, which facilitates viral transduction, however, may hamper T cell fitness and reduce in vivo persistence. "T-Expand" is developed for T cell activation and expansion, comprising dextran-based nanoparticles conjugated with anti-CD3 and anti-CD28 antibodies. The nanoparticles trigger robust polyclonal expansion of human T cells with efficiency in the range of commercial microbeads (Dynabeads™). Engineered in the presence of T-Expand, CD19 CAR T cells display enhanced proliferative capacity, cytotoxicity and persistence in vitro, and furthermore, exhibit potent anti-lymphoma activity in mouse models, resulting in complete tumor clearance at one fourth of the CAR T cell dose. Importantly, T-Expand is biocompatible with no observed toxicity, circumventing removal steps after T cell expansion compared to Dynabeads<sup>TM</sup>. As a biocompatible T cell expansion platform, T-Expand simplifies the manufacturing process while enhancing T cell persistence and functionality, and thereby holds promise for increasing clinical efficacy of CAR T cell therapy.

Nature CommunicationsVol. 17(1)
University of Copenhagen (DK), Leibniz Association (DE), Leibniz Institute for Immunotherapy, Technical University of Denmark (DK)
Openalex Percentile: Top 83%
CAR-T cell therapy research
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