دورية أكاديمية
Combination Immunotherapy with CAR T Cells and Checkpoint Blockade for the Treatment of Solid Tumors.
العنوان: | Combination Immunotherapy with CAR T Cells and Checkpoint Blockade for the Treatment of Solid Tumors. |
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المؤلفون: | Grosser R; Thoracic Service, Department of Surgery, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA., Cherkassky L; Surgical Oncology Service, Department of Surgery, Memorial Sloan Kettering Cancer, New York, NY 10065, USA., Chintala N; Thoracic Service, Department of Surgery, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA., Adusumilli PS; Thoracic Service, Department of Surgery, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA; Center for Cell Engineering, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA. Electronic address: adusumip@mskcc.org. |
المصدر: | Cancer cell [Cancer Cell] 2019 Nov 11; Vol. 36 (5), pp. 471-482. |
نوع المنشور: | Journal Article; Research Support, N.I.H., Extramural; Research Support, U.S. Gov't, Non-P.H.S.; Review |
اللغة: | English |
بيانات الدورية: | Publisher: Cell Press Country of Publication: United States NLM ID: 101130617 Publication Model: Print Cited Medium: Internet ISSN: 1878-3686 (Electronic) Linking ISSN: 15356108 NLM ISO Abbreviation: Cancer Cell Subsets: MEDLINE |
أسماء مطبوعة: | Original Publication: Cambridge, Mass. : Cell Press, c2002- |
مواضيع طبية MeSH: | Antineoplastic Agents, Immunological/*therapeutic use , Costimulatory and Inhibitory T-Cell Receptors/*antagonists & inhibitors , Immunotherapy, Adoptive/*methods , Neoplasms/*therapy , Receptors, Chimeric Antigen/*immunology, Animals ; Antineoplastic Agents, Immunological/pharmacology ; Combined Modality Therapy/methods ; Costimulatory and Inhibitory T-Cell Receptors/immunology ; Costimulatory and Inhibitory T-Cell Receptors/metabolism ; Disease Models, Animal ; Humans ; Neoplasms/immunology ; Neoplasms/pathology ; Randomized Controlled Trials as Topic ; Treatment Outcome ; Tumor Escape/drug effects ; Tumor Escape/immunology ; Tumor Microenvironment/drug effects ; Tumor Microenvironment/immunology |
مستخلص: | Checkpoint blockade (CPB) therapy can elicit durable clinical responses by reactivating an exhausted immune response. However, response rates remain limited, likely secondary to a lack of a tumor-reactive immune infiltrate. Chimeric antigen receptor (CAR) T cells may provide the necessary tumor-targeting immune infiltrate and a highly specific antitumor immune response. This can be further amplified by the addition of CPB agents, which serve to counteract the immune inhibitory environment undermining optimal CAR T cell efficacy. Herein, we review preclinical and clinical combination therapy with CAR T cells and CPB agents, with a focus on solid tumor malignancies. (Copyright © 2019 Elsevier Inc. All rights reserved.) |
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(PMID: 8596936) |
معلومات مُعتمدة: | P30 CA008748 United States CA NCI NIH HHS; R01 CA235667 United States CA NCI NIH HHS; R01 CA236615 United States CA NCI NIH HHS |
فهرسة مساهمة: | Keywords: CAR T cell; PD-1; checkpoint blockade; chimeric antigen receptor; immunotherapy |
المشرفين على المادة: | 0 (Antineoplastic Agents, Immunological) 0 (Costimulatory and Inhibitory T-Cell Receptors) 0 (Receptors, Chimeric Antigen) |
تواريخ الأحداث: | Date Created: 20191113 Date Completed: 20200527 Latest Revision: 20231113 |
رمز التحديث: | 20231215 |
مُعرف محوري في PubMed: | PMC7171534 |
DOI: | 10.1016/j.ccell.2019.09.006 |
PMID: | 31715131 |
قاعدة البيانات: | MEDLINE |
تدمد: | 1878-3686 |
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DOI: | 10.1016/j.ccell.2019.09.006 |