Dextran-based T-cell expansion nanoparticles for manufacturing CAR T cells with augmented efficacy.
1/5 보강
Adoptive T cell therapy using chimeric antigen receptor (CAR) engineered T cells is currently being explored in multiple cancer types beyond leukemia/lymphoma.
APA
Zheng T, Ramanathan K, et al. (2026). Dextran-based T-cell expansion nanoparticles for manufacturing CAR T cells with augmented efficacy.. Nature communications, 17(1), 1103. https://doi.org/10.1038/s41467-025-67868-1
MLA
Zheng T, et al.. "Dextran-based T-cell expansion nanoparticles for manufacturing CAR T cells with augmented efficacy.." Nature communications, vol. 17, no. 1, 2026, pp. 1103.
PMID
41559042
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. 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.
MeSH Terms
Humans; Animals; Dextrans; T-Lymphocytes; Immunotherapy, Adoptive; Receptors, Chimeric Antigen; Nanoparticles; Mice; Antigens, CD19; Cell Proliferation; Lymphocyte Activation; CD3 Complex; CD28 Antigens; Cell Line, Tumor; Xenograft Model Antitumor Assays; Female; Mice, Inbred NOD; Lymphoma
같은 제1저자의 인용 많은 논문 (5)
- Diagnostic performance and generalizability of a clinical-ultrasound radiomics model for predicting extrathyroidal extension in thyroid carcinoma: a retrospective study.
- State-of-the-art review:Cardiac magnetic resonance imaging in primary cardiac tumors.
- Association of HMGB1 expression with prognosis of non-small cell lung cancer: a systematic review and meta-analysis.
- Synergistic inhibitory effects of enzalutamide and its phase I metabolite on UDP-glucuronosyltransferase 1A1 (UGT1A1) and risk prediction of drug-drug interactions.
- Clock genes in pancreatic disease progression: from circadian regulation to dysfunction.