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Sharma et al. Neuroimmunol Neuroinflammation 2018;5:43        Neuroimmunology and
               DOI: 10.20517/2347-8659.2018.51                                   Neuroinflammation




               Review                                                                        Open Access


               CAR-T cell therapy in neuro-oncology: applications
               and toxicity


               Akanksha Sharma , Gustavo De Leon , Alyx Porter , Marie F Grill , Allison Rosenthal , Christine E
                               1,2
                                                                                         2
                                                                        1
                                                3
                                                            1,2
               Brown , Kristin Swanson , Maciej M Mrugala 1,2
                     4
                                     3
               1 Department of Neurology, Mayo Clinic, Phoenix, AZ 85054, USA.
               2 Division of Hematology-Oncology, Mayo Clinic, Phoenix, AZ 85054, USA.
               3 Mathematical Neuro-Oncology Lab, Mayo Clinic, Phoenix, AZ 85054, USA.
               4 Department of Hematology and Hematopoietic Cell Transplantation, T Cell Therapeutics Research Laboratory, City of Hope Beckman
               Research Institute, Duarte, CA 91010, USA.
               Correspondence to: Dr. Maciej M Mrugala, Department of Neurology, 5777 E Mayo Blvd, Mayo Clinic, Phoenix, AZ 85054, USA.
               E-mail: mrugala.maciej@mayo.edu
               How to cite this article: Sharma A, De Leon G, Porter A, Grill MF, Rosenthal A, Brown CE, Swanson K, Mrugala MM. CAR-T cell
               therapy in neuro-oncology: applications and toxicity. Neuroimmunol Neuroinflammation 2018;5:43.
               http://dx.doi.org/10.20517/2347-8659.2018.51

               Received: 25 Aug 2018     First Decision: 13 Sep 2018     Revised: 20 Sep 2018     Accepted: 20 Sep 2018     Published: 18 Oct 2018
               Science Editor: Athanassios P. Kyritsis    Copy Editor: Cai-Hong Wang    Production Editor: Zhong-Yu Guo




               Abstract
               A new era for cancer treatment has been ushered in with the field of cancer immunotherapy. After initial success
               with systemic malignancies, several of these promising treatments are being investigated for efficacy with primary
               and secondary brain tumors. Chimeric antigen receptor (CAR) T cells are being studied, both with systemic infusion
               and direct administration to the tumor and into the cerebrospinal fluid, with promising early results. Systemic CAR-T
               treatment can have serious systemic and neurological toxicities that are important for the practicing neurologist
               and neuro-oncologist to know and understand. This review aims to discuss adoptive cell therapies with a focus on
               CAR-T treatment. We review use of this therapy in brain cancers, particularly malignant glioma, and provide an
               overview of the toxicity of CAR-T treatment and its appropriate management.

               Keywords: CAR-T cell, immunotherapy, brain tumor, cytokine release syndrome





               INTRODUCTION
               The immune system plays many roles in cancer prevention. Not only does it protect against viral infections
               and the development of virus-driven tumors, it also eliminates tumor cells, and rapidly identifies and



                           © The Author(s) 2018. Open Access This article is licensed under a Creative Commons Attribution 4.0
                           International License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use,
                sharing, adaptation, distribution and reproduction in any medium or format, for any purpose, even commercially, as long
                as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license,
                and indicate if changes were made.


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