Use of CAR-T cell therapy, PD-1 blockade, and their combination for the treatment of hematological malignancies

Copyright © 2020 Elsevier Inc. All rights reserved.

Bibliographische Detailangaben
Veröffentlicht in:Clinical immunology (Orlando, Fla.). - 1999. - 214(2020) vom: 01. Mai, Seite 108382
1. Verfasser: Song, Wenting (VerfasserIn)
Weitere Verfasser: Zhang, Mingzhi
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2020
Zugriff auf das übergeordnete Werk:Clinical immunology (Orlando, Fla.)
Schlagworte:Journal Article Research Support, Non-U.S. Gov't Review CAR-T Combination Hematological malignancies PD-1 blockade Antibodies, Monoclonal, Humanized Antineoplastic Agents, Immunological Neoplasm Proteins mehr... PDCD1 protein, human Programmed Cell Death 1 Receptor Nivolumab 31YO63LBSN pembrolizumab DPT0O3T46P
Beschreibung
Zusammenfassung:Copyright © 2020 Elsevier Inc. All rights reserved.
With the successful treatment of B-cell lymphomas using rituximab, a monoclonal antibody targeting CD20, novel immunotherapies have developed rapidly in recent years. Immune checkpoint blockade and chimeric antigen receptor-T (CAR-T) cell therapy, which are antibody-based therapy and cell-based therapy, respectively, show promising efficacy and have been approved by the Food and Drug Administration for treating hematological malignancies. However, considering severe side effects and short-term clinical remission, the combination of CAR-T cell therapy and programmed cell-death protein-1 (PD-1) blockade has been applied to enhance therapeutic efficacy in preclinical models and clinical trials. Herein, we review the mechanism of the two therapies, show their toxicities and clinical use respectively, address their combined application, and discuss the scope of further investigations of this mechanism-based combination therapy
Beschreibung:Date Completed 23.10.2020
Date Revised 23.10.2020
published: Print-Electronic
Citation Status MEDLINE
ISSN:1521-7035
DOI:10.1016/j.clim.2020.108382