مورد إلكتروني

Understanding T cell phenotype for the design of effective chimeric antigen receptor T cell therapies

التفاصيل البيبلوغرافية
العنوان: Understanding T cell phenotype for the design of effective chimeric antigen receptor T cell therapies
المؤلفون: Tantalo, DGM, Oliver, AJ, von Scheidt, B, Harrison, AJ, Mueller, SN, Kershaw, MH, Slaney, CY
بيانات النشر: BMJ PUBLISHING GROUP 2021-05-01
نوع الوثيقة: Electronic Resource
مستخلص: Rapid advances in immunotherapy have identified adoptive cell transfer as one of the most promising approaches for the treatment of cancers. Large numbers of cancer reactive T lymphocytes can be generated ex vivo from patient blood by genetic modification to express chimeric antigen receptors (CAR) specific for tumor-associated antigens. CAR T cells can respond strongly against cancer cells, and adoptive transferred CAR T cells can induce dramatic responses against certain types of cancers. The ability of T cells to respond against disease depends on their ability to localize to sites, persist and exert functions, often in an immunosuppressive microenvironment, and these abilities are reflected in their phenotypes. There is currently intense interest in generating CAR T cells possessing the ideal phenotypes to confer optimal antitumor activity. In this article, we review T cell phenotypes for trafficking, persistence and function, and discuss how culture conditions and genetic makeups can be manipulated to achieve the ideal phenotypes for antitumor activities.
مصطلحات الفهرس: Journal Article
URL: http://hdl.handle.net/11343/278368
الإتاحة: Open access content. Open access content
CC BY-NC
https://creativecommons.org/licenses/by-nc/4.0
أرقام أخرى: UMV oai:jupiter.its.unimelb.edu.au:11343/278368
Tantalo, D. G. M., Oliver, A. J., von Scheidt, B., Harrison, A. J., Mueller, S. N., Kershaw, M. H. & Slaney, C. Y. (2021). Understanding T cell phenotype for the design of effective chimeric antigen receptor T cell therapies. JOURNAL FOR IMMUNOTHERAPY OF CANCER, 9 (5), https://doi.org/10.1136/jitc-2021-002555.
10.1136/jitc-2021-002555
2051-1426
2051-1426
1315717491
المصدر المساهم: UNIV OF MELBOURNE
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رقم الأكسشن: edsoai.on1315717491
قاعدة البيانات: OAIster