The adoptive transfer of engineered T cells for the treatment of cancer, autoimmunity, and infectious disease is a rapidly growing field that has shown great promise. Gene editing holds tremendous potential for further improvements of T cell therapy. Here we review the applications of gene editing in various T cell therapies, focusing on antiviral strategies and cancer immunotherapies, and discuss the challenges and future prospects. Copyright (C) 2017, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, and Genetics Society of China. Published by Elsevier Limited and Science Press. All rights reserved.National Natural Science Foundation of China [31471215]; National High-tech R&D Program (863 Program) [2015A...
The development of clustered regularly interspaced short palindromic repeats (CRISPR) has spurred a ...
While clustered regularly interspaced short palindromic repeats (CRISPR)-based genome editing techni...
Gene transfer technology and its application to human gene therapy greatly expanded in the last deca...
First-generation adoptive T-cell transfer (ACT) administering tumor-infiltrating lymphocytes (TILs),...
First-generation adoptive T-cell transfer (ACT) administering tumor-infiltrating lymphocytes (TILs),...
T cells following genome editing and transformation might be detectable in peripheral blood and tumo...
We present an overview of clinical trials involving gene editing using clustered interspaced short p...
The aim of this manuscript is to discuss the use of some advances in immunotherapies for cancer from...
Genome editing technologies not only provide unprecedented opportunities to study basic cellular sys...
Genome editing technologies not only provide unprecedented opportunities to study basic cellular sys...
Ex vivo manipulations of autologous patient’s cells or gene-engineered cell therapeutics have allowe...
Genome editing tools are being rapidly developed, accelerating many areas of cell and gene therapy r...
International audienceRecent advances in genome editing tools, especially novel developments in the ...
T cell modification with genes that encode chimeric antigen receptors (CAR-T cells) has shown tremen...
Recent early stage clinical trials evaluating the adoptive transfer of patient CD8+ T-cells re-direc...
The development of clustered regularly interspaced short palindromic repeats (CRISPR) has spurred a ...
While clustered regularly interspaced short palindromic repeats (CRISPR)-based genome editing techni...
Gene transfer technology and its application to human gene therapy greatly expanded in the last deca...
First-generation adoptive T-cell transfer (ACT) administering tumor-infiltrating lymphocytes (TILs),...
First-generation adoptive T-cell transfer (ACT) administering tumor-infiltrating lymphocytes (TILs),...
T cells following genome editing and transformation might be detectable in peripheral blood and tumo...
We present an overview of clinical trials involving gene editing using clustered interspaced short p...
The aim of this manuscript is to discuss the use of some advances in immunotherapies for cancer from...
Genome editing technologies not only provide unprecedented opportunities to study basic cellular sys...
Genome editing technologies not only provide unprecedented opportunities to study basic cellular sys...
Ex vivo manipulations of autologous patient’s cells or gene-engineered cell therapeutics have allowe...
Genome editing tools are being rapidly developed, accelerating many areas of cell and gene therapy r...
International audienceRecent advances in genome editing tools, especially novel developments in the ...
T cell modification with genes that encode chimeric antigen receptors (CAR-T cells) has shown tremen...
Recent early stage clinical trials evaluating the adoptive transfer of patient CD8+ T-cells re-direc...
The development of clustered regularly interspaced short palindromic repeats (CRISPR) has spurred a ...
While clustered regularly interspaced short palindromic repeats (CRISPR)-based genome editing techni...
Gene transfer technology and its application to human gene therapy greatly expanded in the last deca...