4.6 Review

Chimeric Antigen Receptor (CAR) T Cell Therapy for Malignant Pleural Mesothelioma (MPM)

期刊

CANCERS
卷 9, 期 9, 页码 -

出版社

MDPI
DOI: 10.3390/cancers9090115

关键词

immunotherapy; chimeric antigen receptor T cells; mesothelioma; adoptive cell transfer

类别

资金

  1. NIH/NCI [K08CA163941]
  2. NIH [P01 CA66726, RO1 CA172921]
  3. NATIONAL CANCER INSTITUTE [K08CA163941, R01CA172921, P01CA066726] Funding Source: NIH RePORTER
  4. NATIONAL INSTITUTE OF ENVIRONMENTAL HEALTH SCIENCES [P30ES013508] Funding Source: NIH RePORTER

向作者/读者索取更多资源

Cancer immunotherapy has now become a recognized approach to treating cancers. In addition to checkpoint blockade, adoptive T cell transfer (ACT) using chimeric antigen receptors (CARs) has shown impressive clinical outcomes in leukemias and is now being explored in solid tumors. CARs are engineered receptors, stably or transiently transduced into T cells, that aim to enhance T cell effector function by recognizing and binding to a specific tumor-associated antigen. In this review, we provide a summary of CAR T cell preclinical studies and clinical trials for malignant pleural mesothelioma (MPM), a rare, locally invasive pleural cancer with poor prognosis. We list other attractive potential targets for CAR T cell therapy for MPM, and discuss augmentation strategies of CAR T cell therapy with other forms of immunotherapy in this disease.

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