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Potent neutralizing human monoclonal antibodies protect from Rift Valley fever encephalitis.
Connors, Kaleigh A; Chapman, Nathaniel S; McMillen, Cynthia M; Hoehl, Ryan M; McGaughey, Jackson J; Frey, Zachary D; Midgett, Morgan; Williams, Connor; Reed, Douglas S; Crowe, James E; Hartman, Amy L.
Afiliación
  • Connors KA; Department of Infectious Diseases and Microbiology, School of Public Health, and.
  • Chapman NS; Center for Vaccine Research, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
  • McMillen CM; Department of Pathology, Microbiology and Immunology, and.
  • Hoehl RM; Vanderbilt Vaccine Center, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
  • McGaughey JJ; Department of Infectious Diseases and Microbiology, School of Public Health, and.
  • Frey ZD; Center for Vaccine Research, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
  • Midgett M; Center for Vaccine Research, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
  • Williams C; Center for Vaccine Research, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
  • Reed DS; Center for Vaccine Research, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
  • Crowe JE; Center for Vaccine Research, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
  • Hartman AL; Center for Vaccine Research, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
JCI Insight ; 9(18)2024 Aug 01.
Article en En | MEDLINE | ID: mdl-39088277
ABSTRACT
Rift Valley fever (RVF) is an emerging arboviral disease affecting both humans and livestock. In humans, RVF displays a spectrum of clinical manifestations, including encephalitis. To date, there are no FDA-approved vaccines or therapeutics for human use, although several are in preclinical development. Few small-animal models of RVF encephalitis exist, further complicating countermeasure assessment. Human mAbs RVFV-140, RVFV-268, and RVFV-379 are recombinant potently neutralizing antibodies that prevent infection by binding the RVFV surface glycoproteins. Previous studies showed that both RVFV-268 and RVFV-140 improve survival in a lethal mouse model of disease, and RVFV-268 has prevented vertical transmission in a pregnant rat model of infection. Despite these successes, evaluation of mAbs in the context of brain disease has been limited. This is the first study to our knowledge to assess neutralizing antibodies for prevention of RVF neurologic disease using a rat model. Administration of RVFV-140, RVFV-268, or RVFV-379 24 hours prior to aerosol exposure to the virulent ZH501 strain of RVFV resulted in substantially enhanced survival and lack of neurological signs of disease. These results using a stringent and highly lethal aerosol infection model support the potential use of human mAbs to prevent the development of RVF encephalitis.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Fiebre del Valle del Rift / Virus de la Fiebre del Valle del Rift / Modelos Animales de Enfermedad / Anticuerpos Neutralizantes / Anticuerpos Monoclonales / Anticuerpos Antivirales Límite: Animals / Female / Humans Idioma: En Revista: JCI Insight / JCI insight Año: 2024 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Fiebre del Valle del Rift / Virus de la Fiebre del Valle del Rift / Modelos Animales de Enfermedad / Anticuerpos Neutralizantes / Anticuerpos Monoclonales / Anticuerpos Antivirales Límite: Animals / Female / Humans Idioma: En Revista: JCI Insight / JCI insight Año: 2024 Tipo del documento: Article