Targeting tumours with genetically enhanced T lymphocytes

被引:414
作者
Sadelain, M
Rivière, I
Brentjens, R
机构
[1] Mem Sloan Kettering Canc Ctr, Dept Med, New York, NY 10021 USA
[2] Mem Sloan Kettering Canc Ctr, Program Immunol, New York, NY 10021 USA
关键词
D O I
10.1038/nrc971
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The genetic modification of T lymphocytes is an important approach to investigating normal T-cell biology and to increasing antitumour immunity. A number of genetic strategies aim to increase the recognition of tumour antigens, enhance antitumour activities and prevent T-cell malfunction. T cells can also be engineered to increase safety, as well as to express markers that can be tracked by non-invasive imaging technologies. Genetically modified T cells are therefore proving to be of great value for basic immunology and experimental immunotherapy.
引用
收藏
页码:35 / 45
页数:11
相关论文
共 50 条
[31]   Tumour-infiltrating cytotoxic T lymphocytes in somatotroph pituitary neuroendocrine tumours [J].
Iacovazzo, Donato ;
Chiloiro, Sabrina ;
Carlsen, Eivind ;
Bianchi, Antonio ;
Giampietro, Antonella ;
Tartaglione, Tommaso ;
Bima, Chiara ;
Bracaccia, Maria Elena ;
Lugli, Francesca ;
Lauretti, Liverana ;
Anile, Carmelo ;
Gessi, Marco ;
Colosimo, Cesare ;
Rindi, Guido ;
Pontecorvi, Alfredo ;
Korbonits, Marta ;
De Marinis, Laura .
ENDOCRINE, 2020, 67 (03) :651-658
[32]   Tumour-infiltrating cytotoxic T lymphocytes in somatotroph pituitary neuroendocrine tumours [J].
Donato Iacovazzo ;
Sabrina Chiloiro ;
Eivind Carlsen ;
Antonio Bianchi ;
Antonella Giampietro ;
Tommaso Tartaglione ;
Chiara Bima ;
Maria Elena Bracaccia ;
Francesca Lugli ;
Liverana Lauretti ;
Carmelo Anile ;
Marco Gessi ;
Cesare Colosimo ;
Guido Rindi ;
Alfredo Pontecorvi ;
Márta Korbonits ;
Laura De Marinis .
Endocrine, 2020, 67 :651-658
[33]   Targeting tumours [radiotherapy] [J].
Greenaway, Beth .
Engineering and Technology, 2008, 3 (17) :44-47
[34]   Targeting tumours with HSV [J].
Fricker, J .
DRUG DISCOVERY TODAY, 2000, 5 (01) :5-6
[35]   Genetically determined gonadal tumours in children [J].
Audí, L ;
Torán, N ;
Piró, C ;
Gussinyé, M ;
Carrascosa, A .
JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM, 2005, 18 :1215-1225
[36]   CD34-based enrichment of genetically engineered human T cells for clinical use results in dramatically enhanced tumor targeting [J].
Norell, Hakan ;
Zhang, Yi ;
McCracken, James ;
da Palma, Telma Martins ;
Lesher, Aaron ;
Liu, Yueying ;
Roszkowski, Jeffrey J. ;
Temple, Anquanette ;
Callender, Glenda G. ;
Clay, Timothy ;
Orentas, Rimas ;
Guevara-Patino, Jose ;
Nishimura, Michael I. .
CANCER IMMUNOLOGY IMMUNOTHERAPY, 2010, 59 (06) :851-862
[37]   CD34-based enrichment of genetically engineered human T cells for clinical use results in dramatically enhanced tumor targeting [J].
Håkan Norell ;
Yi Zhang ;
James McCracken ;
Telma Martins da Palma ;
Aaron Lesher ;
Yueying Liu ;
Jeffrey J. Roszkowski ;
Anquanette Temple ;
Glenda G. Callender ;
Timothy Clay ;
Rimas Orentas ;
José Guevara-Patiño ;
Michael I. Nishimura .
Cancer Immunology, Immunotherapy, 2010, 59 :851-862
[38]   A Platform for the Scalable Derivation of Genetically-Enhanced T and NK Lymphocytes from Naive Human Induced Pluripotent Stem Cells for Cancer Immunotherapy [J].
Clarke, Raedun ;
Kim, William ;
Groff, Brian ;
Abujarour, Ramzey ;
Robinson, Megan ;
Huang, Xiaosong ;
Sahaf, Newsha ;
Raynel, Sarah ;
Rezner, Betsy ;
Robbins, David ;
Guerrettaz, Lisa ;
Shoemaker, Daniel ;
Valamehr, Bahram .
BLOOD, 2015, 126 (23)
[39]   ENHANCED SUSCEPTIBILITY TO HUMAN-IMMUNODEFICIENCY-VIRUS INFECTION IN CD4(+) T-LYMPHOCYTES GENETICALLY DEFICIENT IN CD43 [J].
SRINIVAS, RV ;
SU, T ;
TRIMBLE, LA ;
LIEBERMAN, J ;
ARDMAN, B .
AIDS RESEARCH AND HUMAN RETROVIRUSES, 1995, 11 (09) :1015-1021
[40]   Targeting the tumour vasculature with CAR T-cells for treatment of solid tumours [J].
Sanchez-Nieto, J. M. ;
Guijaro-Leach, J. J. ;
Camicia, R. ;
Keogh, A. ;
Ricardo, C. P. ;
Labbe, R. ;
Petrovic, R. ;
Gargiulo, L. ;
Robinson, J. ;
Zhuang, X. ;
Jinks, E. ;
Whitworth, K. ;
Bystrom, J. ;
Sharif, M. ;
Nagy, Z. ;
Tordo, J. ;
Mccoy, R. ;
Kallmeier, R. ;
Sharpe, M. ;
Bicknell, R. ;
Lee, S. ;
Munye, M. M. .
HUMAN GENE THERAPY, 2019, 30 (08) :A14-A15