| Literature DB >> 28595516 |
Ziqi Tao1, Shuang Li2, Thomas E Ichim3, Junbao Yang4, Neil Riordan5, Venkata Yenugonda4, Ivan Babic4, Santosh Kesari4,6.
Abstract
The clinical success of checkpoint inhibitors has led to a renaissance of interest in cancer immunotherapies. In particular, the possibility of ex vivo expanding autologous lymphocytes that specifically recognize tumor cells has attracted much research and clinical trial interest. In this review, we discuss the historical background of tumor immunotherapy using cell-based approaches, and provide some rationale for overcoming current barriers to success of autologous immunotherapy. An overview of adoptive transfer of lymphocytes, tumor infiltrating lymphocytes and dendritic cell therapies is provided. We conclude with discussing the possibility of gene-manipulating immune cells in order to augment therapeutic activity, including silencing of the immune-suppressive zinc finger orphan nuclear receptor, NR2F6, as an attractive means of overcoming tumor-associated immune suppression.Entities:
Keywords: CAR T-cells; NR2F6; cancer; cellular therapy; immunotherapy
Mesh:
Substances:
Year: 2017 PMID: 28595516 DOI: 10.2217/imt-2016-0086
Source DB: PubMed Journal: Immunotherapy ISSN: 1750-743X Impact factor: 4.196