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Sean A. Van Tongeren

Researcher at United States Army Medical Research Institute of Infectious Diseases

Publications -  21
Citations -  2352

Sean A. Van Tongeren is an academic researcher from United States Army Medical Research Institute of Infectious Diseases. The author has contributed to research in topics: Ebola virus & Marburg virus. The author has an hindex of 12, co-authored 20 publications receiving 1857 citations. Previous affiliations of Sean A. Van Tongeren include United States Department of the Army.

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Therapeutic efficacy of the small molecule GS-5734 against Ebola virus in rhesus monkeys

TL;DR: These results show the first substantive post-exposure protection by a small-molecule antiviral compound against EBOV in nonhuman primates, and the broad-spectrum antiviral activity of GS-5734 in vitro against other pathogenic RNA viruses, including filoviruses, arenavirus, and coronavirus suggests the potential for wider medical use.
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Advanced antisense therapies for postexposure protection against lethal filovirus infections

TL;DR: Administration of positively charged phosphorodiamidate morpholino oligomers (PMOplus), delivered by various dosing strategies initiated 30–60 min after infection, protects >60% of rhesus monkeys against lethal Zaire Ebola virus (ZEBOV) and 100% of cynomolgus monkeysagainst Lake Victoria Marburg virus (MARV) infection.
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Efficacy of favipiravir (T-705) in nonhuman primates infected with Ebola virus or Marburg virus.

TL;DR: Favipiravir is a broad‐spectrum antiviral agent that has demonstrated efficacy against Ebola virus (EBOV) in rodents and in vivo efficacy against two filoviruses, EBOV and Marburg virus (MARV), and its pharmacokinetic profile is evaluated.
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Toll-Like Receptor Agonist Augments Virus-Like Particle-Mediated Protection from Ebola Virus with Transient Immune Activation

TL;DR: This study explores the impact of a stabilized dsRNA mimic, polyICLC, on VLP vaccination of C57BL/6 mice and Hartley guinea pigs and shows that at dose levels as low as 100 ng, the adjuvant increased the efficacy of the vaccine in mice.