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Mesothelin-Targeted CARs: Driving T Cells to Solid Tumors

Journal

CANCER DISCOVERY
Volume 6, Issue 2, Pages 133-146

Publisher

AMER ASSOC CANCER RESEARCH
DOI: 10.1158/2159-8290.CD-15-0583

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Funding

  1. NIH [R21 CA164568-01A1, R21 CA164585-01A1, U54 CA137788, P50 CA086438-13, P30 CA008748]
  2. U.S. Department of Defense [LC110202, BC132124]
  3. Lake Road Foundation
  4. Stand Up To Cancer-Cancer Research Institute Cancer Immunology Translational Cancer Research Grant [SU2C-AACR-DT1012]

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Chimeric antigen receptors (CAR) are synthetic receptors that target T cells to cell-surface antigens and augment T-cell function and persistence. Mesothelin is a cell-surface antigen implicated in tumor invasion, which is highly expressed in mesothelioma and lung, pancreas, breast, ovarian, and other cancers. Its low-level expression in mesothelia, however, commands thoughtful therapeutic interventions. Encouragingly, recent clinical trials evaluating active immunization or immunoconjugates in patients with pancreatic adenocarcinoma or mesothelioma have shown responses without toxicity. Altogether, these findings and preclinical CAR therapy models using either systemic or regional T-cell delivery argue favorably for mesothelin CAR therapy in multiple solid tumors. Significance: Recent success obtained with adoptive transfer of CAR T cells targeting CD19 in patients with refractory hematologic malignancies has generated much enthusiasm for T-cell engineering and raises the prospect of implementing similar strategies for solid tumors. Mesothelin is expressed in a wide range and a high percentage of solid tumors, which we review here in detail. Mesothelin CAR therapy has the potential to treat multiple solid malignancies. (C) 2015 AACR.

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