CAR T-cell immunotherapy: The path from the by-road to the freeway?

被引:37
作者
Whilding, Lynsey M. [1 ]
Maher, John [1 ,2 ,3 ]
机构
[1] Kings Coll London, Kings Hlth Partners Integrated Canc Ctr, Dept Res Oncol, Guys Hosp Campus, London SE1 9RT, England
[2] Royal Free London NHS Fdn Trust, Barnet Hosp, Dept Immunol, Barnet EN5 3DJ, Herts, England
[3] Kings Coll Hosp NHS Fdn Trust, Dept Clin Immunol & Allergy, Denmark Hill, London SE5 9RS, England
基金
英国惠康基金; 英国医学研究理事会;
关键词
Immunotherapy; Cancer; Chimeric antigen receptor; T-cells; Solid tumours; CHIMERIC-ANTIGEN-RECEPTOR; FIBROBLAST ACTIVATION PROTEIN; ACUTE MYELOID-LEUKEMIA; MALIGNANT PLEURAL MESOTHELIOMA; GROWTH-FACTOR RECEPTOR; I CLINICAL-TRIAL; ANTITUMOR-ACTIVITY; TUMOR-CELLS; ADOPTIVE IMMUNOTHERAPY; CYTOKINE RELEASE;
D O I
10.1016/j.molonc.2015.10.012
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Chimeric antigen receptors are genetically encoded artificial fusion molecules that can reprogram the specificity of peripheral blood polyclonal T-cells against a selected cell surface target. Unparallelled clinical efficacy has recently been demonstrated using this approach to treat patients with refractory B-cell malignancy. However, the approach is technically challenging and can elicit severe toxicity in patients. Moreover, solid tumours have largely proven refractory to this approach. In this review, we describe the important structural features of CARs and how this may influence function. Emerging clinical experience is summarized in both solid tumours and haematological malignancies. Finally, we consider the particular challenges imposed by solid tumours to the successful development of CAR T-cell immunotherapy, together with a number of innovative strategies that have been developed in an effort to reverse the balance in favour of therapeutic benefit. Crown Copyright (C) 2015 Published by Elsevier B.V. on behalf of Federation of European Biochemical Societies.
引用
收藏
页码:1994 / 2018
页数:25
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