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Anthony T Power

Researcher at Max Planck Society

Publications -  10
Citations -  1787

Anthony T Power is an academic researcher from Max Planck Society. The author has contributed to research in topics: Oncolytic virus & Vesicular stomatitis virus. The author has an hindex of 8, co-authored 10 publications receiving 1673 citations. Previous affiliations of Anthony T Power include University of Ottawa.

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VSV strains with defects in their ability to shutdown innate immunity are potent systemic anti-cancer agents

TL;DR: Evidence is presented that the attenuated vesicular stomatitis strains, AV1 and AV2, embody all of the traits of an oncolytic virus, which will replicate preferentially in malignant cells, have the ability to treat disseminated metastases, and ultimately be cleared by the patient.
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Vesicular stomatitis virus: re-inventing the bullet

TL;DR: Strains of VSV that induce or direct the production of interferon are superior to wild-type strains of the virus for inducing oncolysis and might also make better vaccine vectors.
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Carrier cell-based delivery of an oncolytic virus circumvents antiviral immunity.

TL;DR: The severe negative impact of the adaptive immune response on the systemic delivery of oncolytic vesicular stomatitis virus (VSV) in an immune-competent murine tumor model is demonstrated, an effect mediated primarily by the neutralization of injected virions by circulating antibodies.
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Radioiodide imaging and radiovirotherapy of multiple myeloma using VSV(Delta51)-NIS, an attenuated vesicular stomatitis virus encoding the sodium iodide symporter gene.

TL;DR: VSV(Delta51)-NIS is a safe oncolytic agent with significant therapeutic potential in multiple myeloma and is shown to have potential in combination radiovirotherapy with (131)I.
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Effects of intravenously administered recombinant vesicular stomatitis virus (VSV(deltaM51)) on multifocal and invasive gliomas

TL;DR: Systemically delivered VSV(deltaM51) was an effective and safe oncolytic agent against laboratory models of multifocal and invasive malignant gliomas, the most challenging clinical manifestations of this disease.