Literature DB >> 29203440

CAR-T cells and combination therapies: What's next in the immunotherapy revolution?

Maria C Ramello1, Eric B Haura2, Daniel Abate-Daga3.   

Abstract

Cancer immunotherapies are dramatically reshaping the clinical management of oncologic patients. For many of these therapies, the guidelines for administration, monitoring, and management of associated toxicities are still being established. This is especially relevant for adoptively transferred, genetically-modified T cells, which have unique pharmacokinetic properties, due to their ability to replicate and persist long-term, following a single administration. Furthermore, in the case of CAR-T cells, the use of synthetic immune receptors may impact signaling pathways involved in T cell function and survival in unexpected ways. We, herein, comment on the most salient aspects of CAR-T cell design and clinical experience in the treatment of solid tumors. In addition, we discuss different possible scenarios for combinations of CAR-T cells and other treatment modalities, with a special emphasis on kinase inhibitors, elaborating on the strategies to maximize synergism. Finally, we discuss some of the technologies that are available to explore the molecular events governing the success of these therapies. The young fields of synthetic and systems biology are likely to be major players in the advancement of CAR-T cell therapies, providing the tools and the knowledge to engineer patients' T lymphocytes into intelligent cancer-fighting micromachines.
Copyright © 2017 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  CAR-T cells; Combination therapies; Solid tumors; Synthetic biology; Systems biology; Targeted-therapies

Mesh:

Substances:

Year:  2017        PMID: 29203440      PMCID: PMC5828987          DOI: 10.1016/j.phrs.2017.11.035

Source DB:  PubMed          Journal:  Pharmacol Res        ISSN: 1043-6618            Impact factor:   7.658


  131 in total

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