| Literature DB >> 27897332 |
Rayne H Rouce1,2, Sandhya Sharma1, Mai Huynh1, Helen E Heslop1.
Abstract
In vitro discoveries have paved the way for bench-to-bedside translation in adoptive T cell immunotherapy, resulting in remarkable clinical responses in a variety of haematological malignancies. Adoptively transferred T cells genetically modified to express CD19 CARs have shown great promise, although many unanswered questions regarding how to optimize T-cell therapies for both safety and efficacy remain. Similarly, T cells that recognize viral or tumour antigens though their native receptors have produced encouraging clinical responses. Honing manufacturing processes will increase the availability of T-cell products, while combining T-cell therapies has the ability to increase complete response rates. Lastly, innovative mechanisms to control these therapies may improve safety profiles while genome editing offers the prospect of modulating T-cell function. This review will focus on recent advances in T-cell immunotherapy, highlighting both clinical and pre-clinical advances, as well as exploring what the future holds.Entities:
Keywords: T cells; immunotherapy; lymphoma
Mesh:
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Year: 2016 PMID: 27897332 PMCID: PMC5318250 DOI: 10.1111/bjh.14470
Source DB: PubMed Journal: Br J Haematol ISSN: 0007-1048 Impact factor: 6.998