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Lookup NU author(s): Dr Lei HuangORCiD,
Emeritus Professor Andrew MellorORCiD
This is the authors' accepted manuscript of an article that has been published in its final definitive form by Elsevier Ireland Ltd., 2019.
For re-use rights please refer to the publisher's terms and conditions.
Cancer immunotherapy is a new and promising option for cancer treatment. Unlike traditional chemo- and radiotherapy, immunotherapy actives host immune system to attack malignancies，and this potentially offers long-term protection from recurrence with less toxicity in comparison to conventional chemo- and radiation therapy. In adoptive CD8+ T cell therapy (ACT), large numbers of tumor-specific T cells are sourced from patients and expanded in vitro and infused back to patients. T cells can be expanded from naturally-induced tumor-specific CD8+ T cells isolated from tumor infiltrating lymphocytes (TIL) or genetically-modified autologous circulating CD8+ T cells. The engineered T cells expressed tumor-specific antigen receptors including chimeric antigen receptors (CARs) and T cell receptors (TCRs), prepared from cultured B and T cell clones, respectively. The most successful ACT, anti-CD19 chimeric antigen receptor T (CAR-T) cell therapy directed against B cell lymphoma, is already approved for use based on evidence of efficacy. Efficacy of solid tumors is not yet forthcoming. This review summarizes current technology developments using ACT in clinical trials. In this review, differences between various ACT approaches are discussed. Furthermore, resistance factors in the tumor microenvironment are also considered, as are immune related adverse effects, critical clinic monitoring parameters and potential mitigation approaches.
Author(s): Jiang X, Xu J, Liu M, Xing H, Wang Z, Huang L, Mellor A, Wang W, Wu S
Publication type: Article
Publication status: Published
Journal: Cancer Letter
Print publication date: 10/10/2019
Online publication date: 26/07/2019
Acceptance date: 23/07/2019
Date deposited: 31/07/2019
ISSN (electronic): 0304-3835
Publisher: Elsevier Ireland Ltd.
PubMed id: 31356845
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