| Literature DB >> 26140980 |
Junping Xie1, Xiaolin Guo2, Fangfang Liu2, Junming Luo3, Fengying Duan3, Xiaonan Tao4.
Abstract
Transduction with recombinant, replication-defective adenoviral (rAd) vectors encoding a transgene is an efficient method for gene transfer into human dendritic cells (DCs). Livin is a good candidate for cancer immunotherapy since it is overexpressed in most common human cancers, poorly expressed in most normal adult tissues. Two splicing variants of livin, designated livin α and livin β, have been identified. In this study, we used human livin α recombinant adenovirus (rAd-hlivin α) to transduced DCs. We found that DCs transduced with rAd-hlivin α (rAd-hlivin α DCs) could effectively induce human livin α specific cytotoxic T lymphocytes (CTL) in vitro against various tumor cell lines.Entities:
Keywords: Dendritic cell; Gene therapy; Livin α; Recombinant adenoviral vector; Tumor cell
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Year: 2015 PMID: 26140980 DOI: 10.1016/j.cellimm.2015.06.003
Source DB: PubMed Journal: Cell Immunol ISSN: 0008-8749 Impact factor: 4.868