Chimpanzee Adenovirus Vaccine Provides Multispecies Protection against Rift Valley Fever

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作者
George M. Warimwe
Joseph Gesharisha
B. Veronica Carr
Simeon Otieno
Kennedy Otingah
Danny Wright
Bryan Charleston
Edward Okoth
Lopez-Gil Elena
Gema Lorenzo
El-Behiry Ayman
Naif K. Alharbi
Musaad A. Al-dubaib
Alejandro Brun
Sarah C. Gilbert
Vishvanath Nene
Adrian V. S. Hill
机构
[1] The Jenner Institute,
[2] University of Oxford,undefined
[3] Centre for Research in Therapeutic Sciences and,undefined
[4] Institute for Healthcare Management,undefined
[5] Strathmore University,undefined
[6] International Livestock Research Institute (ILRI),undefined
[7] The Pirbright Institute,undefined
[8] Pirbright,undefined
[9] Woking,undefined
[10] UK ,undefined
[11] Centro de Investigación en Sanidad Animal,undefined
[12] Instituto Nacional de Investigación y Tecnología Agraria y Alimentaria (INIA-CISA),undefined
[13] Qassim University,undefined
[14] King Abdullah International Research Center,undefined
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摘要
Rift Valley Fever virus (RVFV) causes recurrent outbreaks of acute life-threatening human and livestock illness in Africa and the Arabian Peninsula. No licensed vaccines are currently available for humans and those widely used in livestock have major safety concerns. A ‘One Health’ vaccine development approach, in which the same vaccine is co-developed for multiple susceptible species, is an attractive strategy for RVFV. Here, we utilized a replication-deficient chimpanzee adenovirus vaccine platform with an established human and livestock safety profile, ChAdOx1, to develop a vaccine for use against RVFV in both livestock and humans. We show that single-dose immunization with ChAdOx1-GnGc vaccine, encoding RVFV envelope glycoproteins, elicits high-titre RVFV-neutralizing antibody and provides solid protection against RVFV challenge in the most susceptible natural target species of the virus-sheep, goats and cattle. In addition we demonstrate induction of RVFV-neutralizing antibody by ChAdOx1-GnGc vaccination in dromedary camels, further illustrating the potency of replication-deficient chimpanzee adenovirus vaccine platforms. Thus, ChAdOx1-GnGc warrants evaluation in human clinical trials and could potentially address the unmet human and livestock vaccine needs.
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