Targeting Fibroblast Activation Protein in Tumor Stroma with Chimeric Antigen Receptor T Cells Can Inhibit Tumor Growth and Augment Host Immunity without Severe Toxicity

Cancer Immunology Research - Tập 2 Số 2 - Trang 154-166 - 2014
Liang‐Chuan S. Wang1,2,3,4, Albert Lo1,2,3,4, John Scholler1,2,3,4, Jing Sun1,2,3,4, Rajrupa S. Majumdar1,2,3,4, Veena Kapoor1,2,3,4, Michael Antzis1,2,3,4, Cody E. Cotner1,2,3,4, Laura A. Johnson1,2,3,4, Amy C. Durham1,2,3,4, Charalambos Solomides1,2,3,4, Carl H. June1,2,3, Ellen Puré1,2,3,4, Steven Μ. Albelda1,2,3,4
1Abramson Family Cancer Research Institute
2Authors' Affiliations: 1Thoracic Oncology Research Laboratory; 2Abramson Family Cancer Research Institute; 3Department of Pathology and Laboratory Medicine, Perelman School of Medicine; Departments of 4Animal Biology and 5Pathobiology, School of Veterinary Medicine, University of Pennsylvania; and 6Department of Pathology, Thomas Jefferson University, Philadelphia, Pennsylvania
3Department of Pathology and Laboratory Medicine, Perelman School of Medicine
4Department of Pathology, Thomas Jefferson University, Philadelphia, Pennsylvania

Tóm tắt

Abstract

The majority of chimeric antigen receptor (CAR) T-cell research has focused on attacking cancer cells. Here, we show that targeting the tumor-promoting, nontransformed stromal cells using CAR T cells may offer several advantages. We developed a retroviral CAR construct specific for the mouse fibroblast activation protein (FAP), comprising a single-chain Fv FAP [monoclonal antibody (mAb) 73.3] with the CD8α hinge and transmembrane regions, and the human CD3ζ and 4-1BB activation domains. The transduced muFAP-CAR mouse T cells secreted IFN-γ and killed FAP-expressing 3T3 target cells specifically. Adoptively transferred 73.3-FAP-CAR mouse T cells selectively reduced FAPhi stromal cells and inhibited the growth of multiple types of subcutaneously transplanted tumors in wild-type, but not FAP-null immune-competent syngeneic mice. The antitumor effects could be augmented by multiple injections of the CAR T cells, by using CAR T cells with a deficiency in diacylglycerol kinase, or by combination with a vaccine. A major mechanism of action of the muFAP-CAR T cells was the augmentation of the endogenous CD8+ T-cell antitumor responses. Off-tumor toxicity in our models was minimal following muFAP-CAR T-cell therapy. In summary, inhibiting tumor growth by targeting tumor stroma with adoptively transferred CAR T cells directed to FAP can be safe and effective, suggesting that further clinical development of anti-human FAP-CAR is warranted. Cancer Immunol Res; 2(2); 154–66. ©2013 AACR.

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