Literature DB >> 25425467

Challenges to chimeric antigen receptor (CAR)-T cell therapy for cancer.

Michael S Magee1, Adam E Snook.   

Abstract

Chimeric antigen receptor (CAR)-expressing T cells have demonstrated potent clinical efficacy in patients with B cell malignancies. However, the use of CAR-T cell therapy targeting other cancers has, in part, been limited by both the induction of antigen-specific toxicities targeting normal tissues expressing the target-antigen, and the extreme potency of CAR-T cell treatments resulting in life-threatening cytokine-release syndromes. Herein, we discuss toxicities associated with CAR-T cell therapy in the clinic. Further, we discuss potential clinical interventions to ameliorate these toxicities and the application of preclinical animal models to predict the clinical utility of CAR-T cell therapy.

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Year:  2014        PMID: 25425467

Source DB:  PubMed          Journal:  Discov Med        ISSN: 1539-6509            Impact factor:   2.970


  20 in total

1.  Genetically engineered lymphocytes and adoptive cell therapy: cancer immunotherapy's smart bombs.

Authors:  S K Libutti
Journal:  Cancer Gene Ther       Date:  2015-03       Impact factor: 5.987

Review 2.  New approaches for the immunotherapy of acute myeloid leukemia.

Authors:  Terrence L Geiger; Jeffrey E Rubnitz
Journal:  Discov Med       Date:  2015-04       Impact factor: 2.970

Review 3.  Adverse Effects Associated with Clinical Applications of CAR Engineered T Cells.

Authors:  Zohreh Sadat Badieyan; Sayed Shahabuddin Hoseini
Journal:  Arch Immunol Ther Exp (Warsz)       Date:  2018-02-09       Impact factor: 4.291

4.  Epigenetic suppression of the antitumor cytotoxicity of NK cells by histone deacetylase inhibitor valproic acid.

Authors:  Xiumin Shi; Min Li; Meizi Cui; Chao Niu; Jianting Xu; Lei Zhou; Wei Li; Yushun Gao; Weisheng Kong; Jiuwei Cui; Jifan Hu; Haofan Jin
Journal:  Am J Cancer Res       Date:  2016-02-15       Impact factor: 6.166

Review 5.  Chimeric antigen receptor-engineered natural killer and natural killer T cells for cancer immunotherapy.

Authors:  Dominique Bollino; Tonya J Webb
Journal:  Transl Res       Date:  2017-06-09       Impact factor: 7.012

Review 6.  CD19 chimeric antigen receptor (CD19 CAR)-redirected adoptive T-cell immunotherapy for the treatment of relapsed or refractory B-cell Non-Hodgkin's Lymphomas.

Authors:  Alexandra S Onea; Ali R Jazirehi
Journal:  Am J Cancer Res       Date:  2016-01-15       Impact factor: 6.166

7.  The Antitumor Efficacy of IL2/IL21-Cultured Polyfunctional Neu-Specific T Cells Is TNFα/IL17 Dependent.

Authors:  Vy Phan-Lai; Yushe Dang; Ekram Gad; Jennifer Childs; Mary L Disis
Journal:  Clin Cancer Res       Date:  2015-12-09       Impact factor: 12.531

Review 8.  A new insight in chimeric antigen receptor-engineered T cells for cancer immunotherapy.

Authors:  Erhao Zhang; Hanmei Xu
Journal:  J Hematol Oncol       Date:  2017-01-03       Impact factor: 17.388

9.  Engineering T Cells with Customized Therapeutic Response Programs Using Synthetic Notch Receptors.

Authors:  Kole T Roybal; Jasper Z Williams; Leonardo Morsut; Levi J Rupp; Isabel Kolinko; Joseph H Choe; Whitney J Walker; Krista A McNally; Wendell A Lim
Journal:  Cell       Date:  2016-09-29       Impact factor: 41.582

Review 10.  The cnidarian origin of the proto-oncogenes NF-κB/STAT and WNT-like oncogenic pathway drives the ctenophores (Review).

Authors:  Joseph G Sinkovics
Journal:  Int J Oncol       Date:  2015-07-23       Impact factor: 5.650

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