Treating cancer with genetically engineered T cells

Tristen S. Park, Steven A. Rosenberg, Richard A. Morgan

Research output: Contribution to journalReview articlepeer-review

Abstract

Administration of ex vivo cultured, naturally occurring tumor-infiltrating lymphocytes (TILs) has been shown to mediate durable regression of melanoma tumors. However, the generation of TILs is not possible in all patients and there has been limited success in generating TIL in other cancers. Advances in genetic engineering have overcome these limitations by introducing tumor-antigen-targeting receptors into human T lymphocytes. Physicians can now genetically engineer lymphocytes to express highly active T-cell receptors (TCRs) or chimeric antigen receptors (CARs) targeting a variety of tumor antigens expressed in cancer patients. In this review, we discuss the development of TCR and CAR gene transfer technology and the expansion of these therapies into different cancers with the recent demonstration of the clinical efficacy of these treatments.

Original languageEnglish (US)
Pages (from-to)550-557
Number of pages8
JournalTrends in Biotechnology
Volume29
Issue number11
DOIs
StatePublished - Nov 1 2011

ASJC Scopus subject areas

  • Biotechnology
  • Bioengineering

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