Pharmaron scientific poster on non-clinical safety evaluation of nanoparticle-delivered CAR-T cells. Call-to-action button says "Download Poster."

Poster Authors:

Yawen Bu; Xiaonan Liang; Jufeng Wang; Fan Yi

Pharmaron (Beijing) TSP Services Limited. Beijing, China.

Chimeric antigen receptor (CAR) T cell therapy is a promising cancer treatment approach. However, traditional CAR-T engineering relies on viral vectors, which pose several challenges, including permanent CAR expression, high production costs, and safety concerns such as cytokine release syndrome and neurotoxicity. mRNA-lipid nanoparticle (mRNA-LNP) delivery is a cost-effective alternative, enabling temporary CAR expression and reduced toxicity.

In this study, we assessed mRNA-LNP-delivered CAR-T cells in a myeloma mouse model, investigating:

  • CAR-T cell efficacy
  • Biodistribution
  • Cytokine analysis
  • Immunophenotyping
  • Ophthalmological, clinical, and histological pathology

Download our CAR-T cell toxicology study.