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10.3390/v10030108

http://scihub22266oqcxt.onion/10.3390/v10030108
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C5869501!5869501!29498639
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suck abstract from ncbi


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pmid29498639      Viruses 2018 ; 10 (3): ä
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  • The Oncolytic Virus VSV-GP Is Effective against Malignant Melanoma #MMPMID29498639
  • Kimpel J; Urbiola C; Koske I; Tober R; Banki Z; Wollmann G; von Laer D
  • Viruses 2018[Mar]; 10 (3): ä PMID29498639show ga
  • Previously, we described VSV-GP, a modified version of the vesicular stomatitis virus, as a non-neurotoxic oncolytic virus that is effective for the treatment of malignant glioblastoma and ovarian cancer. Here, we evaluate the therapeutic efficacy of VSV-GP for malignant melanoma. All of the human, mouse, and canine melanoma cell lines that were tested, alongside most primary human melanoma cultures, were infected by VSV-GP and efficiently killed. Additionally, we found that VSV-GP prolonged the survival of mice in both a xenograft and a syngeneic mouse model. However, only a few mice survived with long-term tumor remission. When we analyzed the factors that might limit VSV-GP?s efficacy, we found that vector-neutralizing antibodies did not play a role in this context, as even after eight subsequent immunizations and an observation time of 42 weeks, no vector-neutralizing antibodies were induced in VSV-GP immunized mice. In contrast, the type I IFN response might have contributed to the reduced efficacy of the therapy, as both of the cell lines that were used for the mouse models were able to mount a protective IFN response. Nevertheless, early treatment with VSV-GP also reduced the number and size of lung metastases in a syngeneic B16 mouse model. In summary, VSV-GP is a potent candidate for the treatment of malignant melanoma; however, factors limiting the efficacy of the virus need to be further explored.
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