T cell engineering as therapy for cancer and HIV: our synthetic future
It is now well established that the immune system can control and eliminate cancer cells. Adoptive T cell transfer has the potential to overcome the significant limitations associated with vaccine-based strategies in patients who are often immune compromised. Application of the emerging discipline o...
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Published in | Philosophical transactions of the Royal Society of London. Series B. Biological sciences Vol. 370; no. 1680; p. 20140374 |
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Main Authors | , |
Format | Journal Article |
Language | English |
Published |
England
The Royal Society
19.10.2015
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Subjects | |
Online Access | Get full text |
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Summary: | It is now well established that the immune system can control and eliminate cancer cells. Adoptive T cell transfer has the potential to overcome the significant limitations associated with vaccine-based strategies in patients who are often immune compromised. Application of the emerging discipline of synthetic biology to cancer, which combines elements of genetic engineering and molecular biology to create new biological structures with enhanced functionalities, is the subject of this overview. Various chimeric antigen receptor designs, manufacturing processes and study populations, among other variables, have been tested and reported in recent clinical trials. Many questions remain in the field of engineered T cells, but the encouraging response rates pave a wide road for future investigation into fields as diverse as cancer and chronic infections. |
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Bibliography: | Discussion meeting issue ‘Cells: from Robert Hooke to cell therapy—a 350 year journey’ organized and edited by Johan Hyllner, Chris Mason and Ian Wilmut ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 ObjectType-Review-3 content type line 23 One contribution of 13 to a discussion meeting issue ‘Cells: from Robert Hooke to cell therapy—a 350 year journey’. |
ISSN: | 0962-8436 1471-2970 1471-2970 |
DOI: | 10.1098/rstb.2014.0374 |