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Identification of Combinations of Approved Drugs With Synergistic Activity Against Ebola Virus in Cell Cultures.
Dyall, Julie; Nelson, Elizabeth A; DeWald, Lisa Evans; Guha, Rajarshi; Hart, Brit J; Zhou, Huanying; Postnikova, Elena; Logue, James; Vargas, Walter M; Gross, Robin; Michelotti, Julia; Deiuliis, Nicole; Bennett, Richard S; Crozier, Ian; Holbrook, Michael R; Morris, Patrick J; Klumpp-Thomas, Carleen; McKnight, Crystal; Mierzwa, Tim; Shinn, Paul; Glass, Pamela J; Johansen, Lisa M; Jahrling, Peter B; Hensley, Lisa E; Olinger, Gene G; Thomas, Craig; White, Judith M.
Afiliação
  • Dyall J; Integrated Research Facility, Division of Clinical Research, Frederick.
  • Nelson EA; Department of Cell Biology, University of Virginia, Charlottesville.
  • DeWald LE; Integrated Research Facility, Division of Clinical Research, Frederick.
  • Guha R; Division of Preclinical Innovation, National Center for Advancing Translational Sciences, National Institutes of Health, Bethesda, Maryland.
  • Hart BJ; Integrated Research Facility, Division of Clinical Research, Frederick.
  • Zhou H; Integrated Research Facility, Division of Clinical Research, Frederick.
  • Postnikova E; Integrated Research Facility, Division of Clinical Research, Frederick.
  • Logue J; Integrated Research Facility, Division of Clinical Research, Frederick.
  • Vargas WM; Integrated Research Facility, Division of Clinical Research, Frederick.
  • Gross R; Integrated Research Facility, Division of Clinical Research, Frederick.
  • Michelotti J; Integrated Research Facility, Division of Clinical Research, Frederick.
  • Deiuliis N; Integrated Research Facility, Division of Clinical Research, Frederick.
  • Bennett RS; Integrated Research Facility, Division of Clinical Research, Frederick.
  • Crozier I; Integrated Research Facility, Division of Clinical Research, Frederick.
  • Holbrook MR; Integrated Research Facility, Division of Clinical Research, Frederick.
  • Morris PJ; Division of Preclinical Innovation, National Center for Advancing Translational Sciences, National Institutes of Health, Bethesda, Maryland.
  • Klumpp-Thomas C; Division of Preclinical Innovation, National Center for Advancing Translational Sciences, National Institutes of Health, Bethesda, Maryland.
  • McKnight C; Division of Preclinical Innovation, National Center for Advancing Translational Sciences, National Institutes of Health, Bethesda, Maryland.
  • Mierzwa T; Division of Preclinical Innovation, National Center for Advancing Translational Sciences, National Institutes of Health, Bethesda, Maryland.
  • Shinn P; Division of Preclinical Innovation, National Center for Advancing Translational Sciences, National Institutes of Health, Bethesda, Maryland.
  • Glass PJ; Virology Division, United States Army Medical Research Institute of Infectious Diseases, Frederick.
  • Johansen LM; Zalicus, Cambridge, Massachusetts.
  • Jahrling PB; Integrated Research Facility, Division of Clinical Research, Frederick.
  • Hensley LE; Emerging Viral Pathogens Section, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Frederick.
  • Olinger GG; Integrated Research Facility, Division of Clinical Research, Frederick.
  • Thomas C; Integrated Research Facility, Division of Clinical Research, Frederick.
  • White JM; Division of Preclinical Innovation, National Center for Advancing Translational Sciences, National Institutes of Health, Bethesda, Maryland.
J Infect Dis ; 218(suppl_5): S672-S678, 2018 11 22.
Article em En | MEDLINE | ID: mdl-29939303
ABSTRACT

Background:

A need to develop therapeutics to treat Ebola virus disease patients in remote and resource-challenged settings remains in the wake of the 2013-2016 epidemic in West Africa. Toward this goal, we screened drugs under consideration as treatment options and other drugs of interest, most being small molecules approved by the Food and Drug Administration. Drugs demonstrating in vitro antiviral activity were advanced for evaluation in combinations because of advantages often provided by drug cocktails.

Methods:

Drugs were screened for blockade of Ebola virus infection in cultured cells. Twelve drugs were tested in all (78 pair-wise) combinations, and 3 were tested in a subset of combinations.

Results:

Multiple synergistic drug pairs emerged, with the majority comprising 2 entry inhibitors. For the pairs of entry inhibitors studied, synergy was demonstrated at the level of virus entry into host cells. Highly synergistic pairs included aripiprazole/piperacetazine, sertraline/toremifene, sertraline/bepridil, and amodiaquine/clomiphene.

Conclusions:

Our study shows the feasibility of identifying pairs of approved drugs that synergistically block Ebola virus infection in cell cultures. We discuss our findings in terms of the theoretic ability of these or alternate combinations to reach therapeutic levels. Future research will assess selected combinations in small-animal models of Ebola virus disease.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Antivirais / Ebolavirus Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Animals Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Antivirais / Ebolavirus Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Animals Idioma: En Ano de publicação: 2018 Tipo de documento: Article