Toward <i>In Vivo</i> CAR T Cell Therapy: Perfecting CAR and Lipid Nanoparticle Design

CAR T cell therapy represents a leading therapeutic modality in the treatment of hematological cancers. However, conventional ex vivo manufacturing processes are extremely complex, costly, and time-consuming. Hence, <i>in vivo</i> CAR-T cell therapy represents a promising alternative, where T cells are genetically modified directly within the patient. This novel approach requires the careful design of three modular and interdependent nanoscale parameters: CAR architecture, targeted lipid nanoparticle delivery systems, and nucleic acid cargo format. Each component is highly modular, therefore systematic optimization can enhance the safety and efficacy of <i>in vivo</i> CAR T cell generation. Here, we review the molecular and mechanistic principles underlying this therapeutic strategy, emphasizing how these nanoscale design features govern CAR T cell production and functional performance in vivo. Advancing our understanding of these parameters is critical to developing efficient, safe, and clinically translatable in vivo CAR T cell cancer therapies.

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Publication Details

Journal
Nano Letters
Published
2026-02-11
DOI
https://doi.org/10.1021/acs.nanolett.5c05535
Primary Topic
CAR-T cell therapy research
Type
article
Field-Weighted Citation Impact
0.00
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article

Toward In Vivo CAR T Cell Therapy: Perfecting CAR and Lipid Nanoparticle Design

Schiffelers Rm, Ludovica Sciuto, Sander A. A. Kooijmans
Nano Letters
CAR-T cell therapy research
article

Toward In Vivo CAR T Cell Therapy: Perfecting CAR and Lipid Nanoparticle Design

Schiffelers Rm, Ludovica Sciuto, Sander A. A. Kooijmans
article en

Abstract

CAR T cell therapy represents a leading therapeutic modality in the treatment of hematological cancers. However, conventional ex vivo manufacturing processes are extremely complex, costly, and time-consuming. Hence, <i>in vivo</i> CAR-T cell therapy represents a promising alternative, where T cells are genetically modified directly within the patient. This novel approach requires the careful design of three modular and interdependent nanoscale parameters: CAR architecture, targeted lipid nanoparticle delivery systems, and nucleic acid cargo format. Each component is highly modular, therefore systematic optimization can enhance the safety and efficacy of <i>in vivo</i> CAR T cell generation. Here, we review the molecular and mechanistic principles underlying this therapeutic strategy, emphasizing how these nanoscale design features govern CAR T cell production and functional performance in vivo. Advancing our understanding of these parameters is critical to developing efficient, safe, and clinically translatable in vivo CAR T cell cancer therapies.

Nano LettersVol. 26(7)
Utrecht University (NL), Heidelberg University (DE), University Hospital Heidelberg (DE), University Medical Center Utrecht (NL), Wilhelmina Children's Hospital (NL), Shell (Netherlands) (NL)
Openalex Percentile: Top 59%
CAR-T cell therapy research
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