Mesothelin-Targeted CARs: Driving T Cells to Solid Tumors

被引:394
作者
Morello, Aurore [1 ]
Sadelain, Michel [1 ]
Adusumilli, Prasad S. [1 ,2 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Ctr Cell Engn, New York, NY 10065 USA
[2] Mem Sloan Kettering Canc Ctr, Dept Surg, Thorac Serv, New York, NY 10065 USA
关键词
CHIMERIC ANTIGEN RECEPTORS; HUMAN MONOCLONAL-ANTIBODY; ANTITUMOR-ACTIVITY; PHASE-I; OVARIAN-CANCER; ADOPTIVE IMMUNOTHERAPY; PLEURAL MESOTHELIOMA; SELECTIVE EXPANSION; SERUM MESOTHELIN; HIGH-AFFINITY;
D O I
10.1158/2159-8290.CD-15-0583
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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.
引用
收藏
页码:133 / 146
页数:14
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