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Chikungunya vaccine candidate is highly attenuated and protects nonhuman primates against telemetrically monitored disease following a single dose.
Roy, Chad J; Adams, A Paige; Wang, Eryu; Plante, Kenneth; Gorchakov, Rodion; Seymour, Robert L; Vinet-Oliphant, Heather; Weaver, Scott C.
Afiliación
  • Roy CJ; Division of Microbiology, Tulane National Primate Research Center, Covington, Louisiana.
  • Adams AP; Institute for Human Infections and Immunity, Sealy Center for Vaccine Development Department of Pathology, University of Texas Medical Branch, Galveston, Texas.
  • Wang E; Institute for Human Infections and Immunity, Sealy Center for Vaccine Development Department of Pathology, University of Texas Medical Branch, Galveston, Texas.
  • Plante K; Institute for Human Infections and Immunity, Sealy Center for Vaccine Development Department of Pathology, University of Texas Medical Branch, Galveston, Texas.
  • Gorchakov R; Institute for Human Infections and Immunity, Sealy Center for Vaccine Development Department of Pathology, University of Texas Medical Branch, Galveston, Texas.
  • Seymour RL; Institute for Human Infections and Immunity, Sealy Center for Vaccine Development Department of Pathology, University of Texas Medical Branch, Galveston, Texas.
  • Vinet-Oliphant H; Division of Veterinary Medicine, Tulane National Primate Research Center, Covington, Louisiana.
  • Weaver SC; Institute for Human Infections and Immunity, Sealy Center for Vaccine Development Department of Pathology, University of Texas Medical Branch, Galveston, Texas.
J Infect Dis ; 209(12): 1891-9, 2014 Jun 15.
Article en En | MEDLINE | ID: mdl-24403555
Chikungunya virus (CHIKV) is a mosquito-borne alphavirus that causes major epidemics of rash, fever, and debilitating arthritis. Currently, there are no vaccines or antivirals available for prevention or treatment. We therefore generated 2 live-attenuated vaccine candidates based on the insertion of a picornavirus internal ribosome entry site (IRES) sequence into the genome of CHIKV. Vaccination of cynomolgus macaques with a single dose of either vaccine produced no signs of disease but was highly immunogenic. After challenge with a subcutaneous inoculation of wild-type CHIKV, both vaccine candidates prevented the development of detectable viremia. Protected animals also exhibited no significant changes in core body temperature or cardiovascular rhythm, whereas sham-vaccinated animals showed hyperthermia, followed by sustained hypothermia, as well as significant changes in heart rate. These CHIKV/IRES vaccine candidates appear to be safe and efficacious, supporting their strong potential as human vaccines to protect against CHIKV infection and reduce transmission and further spread.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Vacunas Virales / Virus Chikungunya / Infecciones por Alphavirus / Macaca fascicularis Límite: Animals Idioma: En Revista: J Infect Dis Año: 2014 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Vacunas Virales / Virus Chikungunya / Infecciones por Alphavirus / Macaca fascicularis Límite: Animals Idioma: En Revista: J Infect Dis Año: 2014 Tipo del documento: Article