Abstract

While CAR therapy has begun to demonstrate efficacy, cell-engineering techniques that result in permanent genomic modification carry several safety concerns. CAR expression driven by RNA creates a platform for delivery of highly-active cell therapy while avoiding long-term CAR-driven toxicity. Using models of pediatric neuroblastoma, we have found that RNA CAR T cell activity is limited by ineffective tumor infiltration.

Original languageEnglish
Pages (from-to)1-3
Number of pages3
JournalOncoImmunology
Volume3
Issue number12
DOIs
StatePublished - Dec 2 2014

Keywords

  • GD2
  • RNA
  • chimeric antigen receptors
  • pediatrics
  • solid tumors

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