4.7 Article

Development of T Cells Redirected to Glypican-3 for the Treatment of Hepatocellular Carcinoma

Journal

CLINICAL CANCER RESEARCH
Volume 20, Issue 24, Pages 6418-6428

Publisher

AMER ASSOC CANCER RESEARCH
DOI: 10.1158/1078-0432.CCR-14-1170

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Funding

  1. Twelfth Five-year Plan for Science & Technology Research of China [2012ZX09103-301-005, 2012ZX10002]
  2. Research Fund of the State Key Laboratory of Oncogenes and Related Genes [91-14-12]
  3. Shanghai Science and Technology Development Funds [12JC1408300]
  4. Shanghai Rising-Star Program (A type) [13QA1403300]
  5. One Hundred Talents Scientific Research Projects of Health System in Shanghai [XBR2013123]

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Purpose: The aim of our study is to elucidate whether T cells expressing GPC3-targeted chimeric antigen receptor (CAR) can efficiently eliminate GPC3-positive HCC cells and their potential in the treatment of HCC. Experimental Design: T cells expressing a first-generation and third-generation GPC3-targeted CAR were prepared using lentiviral vector transduction. The in vitro and in vivo cytotoxic activities of the genetically engineered CAR T cells were evaluated against various HCC cell lines. Results: GPC3-targeted CAR T cells could efficiently kill GPC3-positive HCC cells but not GPC3-negative cells in vitro. These cytotoxic activities seemed to be positively correlated with GPC3 expression levels in the target cells. In addition, T cells expressing the third-generation GPC3-targeted CAR could eradicate HCC xenografts with high level of GPC3 expression and efficiently suppress the growth of HCC xenografts with low GPC3 expression level in vivo. The survival of the mice bearing established orthotopic Huh-7 xenografts was significantly prolonged by the treatment with the third-generation GPC3-targeted CAR T cells. Conclusions: GPC3-targeted CAR T cells could potently eliminate GPC3-positive HCC cells, thereby providing a promising therapeutic intervention for GPC3-positive HCC. (C)2014 AACR.

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