Immunostimulatory Profile of Cancer Cell Death by the AdV-Lumc007-Derived Oncolytic Virus 'GoraVir' in Cultured Pancreatic Cancer Cells

被引:1
作者
Bots, Selas T. F. [1 ]
Landman, Sanne L. L. [1 ]
Rabelink, Martijn J. W. E. [1 ]
van den Wollenberg, Diana J. M. [1 ]
Hoeben, Rob C. C. [1 ]
机构
[1] Leiden Univ, Med Ctr, Dept Cell & Chem Biol, NL-2333 ZC Leiden, Netherlands
来源
VIRUSES-BASEL | 2023年 / 15卷 / 02期
关键词
pancreatic ductal adenocarcinoma; oncolytic virus; non-human primate adenovirus; immunogenic cell death; STING; ADENOVIRUS; PROTEIN;
D O I
10.3390/v15020283
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Pancreatic ductal adenocarcinoma (PDAC) is a highly aggressive malignancy which shows unparalleled therapeutic resistance. Oncolytic viruses have emerged as a new treatment approach and convey their antitumor activity through lysis of cancer cells. The therapeutic efficacy of oncolytic viruses is largely dependent on the induction of immunogenic cell death (ICD) and the subsequent antitumor immune responses. However, the concurrent generation of antiviral immune responses may also limit the a virus' therapeutic window. GoraVir is a new oncolytic adenovirus derived from the Human Adenovirus B (HAdV-B) isolate AdV-lumc007 which was isolated from a gorilla and has demonstrated excellent lytic activity in both in vitro and in vivo models of PDAC. In this study, we characterized the immunostimulatory profile of cancer cell death induced by GoraVir and the concerted cellular antiviral responses in three conventional pancreatic cancer cell lines. While GoraVir was shown to induce late apoptotic/necrotic cell death at earlier time points post infection than the human adenovirus type 5 (HAdV-C5), similar levels of ICD markers were expressed. Moreover, GoraVir was shown to induce ICD not dependent on STING expression and regardless of subsequent antiviral responses. Together, these data demonstrate that GoraVir is an excellent candidate for use in oncolytic virotherapy.
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页数:13
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