Toward <i>In Vivo</i> CAR T Cell Therapy: Perfecting CAR and Lipid Nanoparticle Design.
review · Level V
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- Record sourced from PubMed, PMID 41672452.
- Also identified by DOI 10.1021/acs.nanolett.5c05535 and PMC identifier 12947888.
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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.
Medical subject headings
- Nanoparticles
- Immunotherapy, Adoptive
- Receptors, Chimeric Antigen
- T-Lymphocytes
- Lipids
- Hematologic Neoplasms