Pre-Existing HSV-1 Immunity Enhances Anticancer Efficacy of a Novel Immune-Stimulating Oncolytic Virus

• Published in: Viruses 2022-10, Vol.14 (11), p.2327
• Main Authors: Ding, Jun, Murad, Yanal M, Sun, Yi, Lee, I-Fang, Samudio, Ismael, Liu, Xiaohu, Jia, William Wei-Guo, Zhao, Ronghua
• Format: Article
• Language: English
• Subjects: Animal models; Animals; Antibodies; Antitumor activity; Biotechnology industry; Cancer; CD34 antigen; Chemotherapy; Cholangiocarcinoma; Disease Models, Animal; Enzyme-linked immunosorbent assay; Gemcitabine; Herpes simplex; Herpes viruses; Herpesvirus 1, Human - genetics; Histocompatibility antigen HLA; HSV-1; Humans; Immunity; Immunity (Disease); Immunization; immunotherapy; Laboratory animals; Lymphocytes T; Lysis; Mice; Neoplasms - therapy; Oncolysis; Oncolytic Virotherapy - methods; oncolytic viruses; Oncolytic Viruses - physiology; Patients; Peptides; Regulatory approval; Software; Statistical analysis; Tumors; Viruses; Xenografts
• ISSN: 1999-4915; 1999-4915
• DOI: 10.3390/v14112327

Oncolytic viruses (OVs) can specifically replicate in the host and cause cancer cell lysis while inducing an antitumor immune response. The aim of this study is to investigate the impact of either pre-existing immunity against herpes simplex virus type-1 (HSV-1) or multicycle treatment with OVs on anticancer efficacy of VG161, an HSV-1 OV in phase 2 clinical trial. VG161 efficacy was tested in CT26 mouse models by comparing the efficacy and immune response in naïve mice or in mice that were immunized with VG161. Moreover, VG161 efficacy in HLA-matched CD34+ humanized intrahepatic cholangiocarcinoma (ICC) patient-derived xenograft (PDX) models was also tested in multicycle treatment and was compared to standard chemotherapy for this type of cancer (gemcitabine). The HSV-1-immunized mice significantly inhibited tumor growth in VG161-treated mice compared to control naïve treated mice. RNA expression profiling and ELISPOT analyses indicated changes in the tumor's immune profile in the immunized and treated group compared to naïve and treated mice, as well as enhanced T cell function depicted by higher numbers of tumor specific lymphocytes, which was enhanced by immunization. In the ICC PDX model, repeated treatment of VG161 with 2 or 3 cycles seemed to increase the anticancer efficacy of VG161. In conclusion, the anticancer efficacy of VG161 can be enhanced by pre-immunization with HSV-1 and multicycle administration when the virus is given intratumorally, indicating that pre-existing antiviral immunity might enhance OV-induced antitumor immunity. Our results suggest potential clinical benefits of HSV-1-based OV therapy in HSV-1-seropositive patients and multicycle administration of VG161 for long-term maintenance treatment.