Gamma-delta T cells are optimal immune cell carrier vehicles for adenovirus vector-based gene therapy
Author:
Affiliation:
1. Department of Urology, Showa University School of Medicine
Publisher
The Showa University Society
Subject
General Medicine
Link
https://www.jstage.jst.go.jp/article/sujms/35/3/35_103/_pdf
Reference28 articles.
1. 1. Yeh P, Perricaudet M. Advances in adenoviral vectors: from genetic engineering to their biology. FASEB J. 1997;11:615-623.
2. 2. Kovesdi I, Brough DE, Bruder JT, et al. Adenoviral vectors for gene transfer. Curr Opin Biotechnol. 1997;8:583-589.
3. 3. Dwyer RM, Schatz SM, Bergert ER, et al. A preclinical large animal model of adenovirus-mediated expression of the sodium-iodide symporter for radioiodide imaging and therapy of locally recurrent prostate cancer. Mol Ther. 2005;12:835-841.
4. 4. Freytag SO, Zhang Y, Siddiqui F. Preclinical toxicology of oncolytic adenovirus-mediated cytotoxic and interleukin-12 gene therapy for prostate cancer. Mol Ther Oncolytics. 2015;2:15006.
5. 5. Freytag SO, Khil M, Stricker H, et al. Phase I study of replication-competent adenovirus-mediated double suicide gene therapy for the treatment of locally recurrent prostate cancer. Cancer Res. 2002;62:4968-4976.
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