A next generation vaccine against human rabies based on a single dose of a chimpanzee adenovirus vector serotype C.
Adenoviruses, Simian
/ genetics
Animals
Antigens, Viral
Female
Genetic Vectors
/ genetics
Humans
Macaca fascicularis
Mice
Pan troglodytes
/ virology
Post-Exposure Prophylaxis
Rabbits
Rabies
/ prevention & control
Rabies Vaccines
/ immunology
Rabies virus
/ genetics
Serogroup
Vaccination
Vaccines, Synthetic
/ immunology
Zoonoses
Journal
PLoS neglected tropical diseases
ISSN: 1935-2735
Titre abrégé: PLoS Negl Trop Dis
Pays: United States
ID NLM: 101291488
Informations de publication
Date de publication:
07 2020
07 2020
Historique:
received:
27
09
2019
accepted:
05
06
2020
entrez:
16
7
2020
pubmed:
16
7
2020
medline:
21
8
2020
Statut:
epublish
Résumé
Rabies, caused by RNA viruses in the Genus Lyssavirus, is the most fatal of all infectious diseases. This neglected zoonosis remains a major public health problem in developing countries, causing the death of an estimated 25,000-159,000 people each year, with more than half of them in children. The high incidence of human rabies in spite of effective vaccines is mainly linked to the lack of compliance with the complicated administration schedule, inadequacies of the community public health system for local administration by the parenteral route and the overall costs of the vaccine. The goal of our work was the development of a simple, affordable and effective vaccine strategy to prevent human rabies virus infection. This next generation vaccine is based on a replication-defective chimpanzee adenovirus vector belonging to group C, ChAd155-RG, which encodes the rabies glycoprotein (G). We demonstrate here that a single dose of this vaccine induces protective efficacy in a murine model of rabies challenge and elicits strong and durable neutralizing antibody responses in vaccinated non-human primates. Importantly, we demonstrate that one dose of a commercial rabies vaccine effectively boosts the neutralizing antibody responses induced by ChAd155-RG in vaccinated monkeys, showing the compatibility of the novel vectored vaccine with the current post-exposure prophylaxis in the event of rabies virus exposure. Finally, we demonstrate that antibodies induced by ChAd155-RG can also neutralize European bat lyssaviruses 1 and 2 (EBLV-1 and EBLV-2) found in bat reservoirs.
Identifiants
pubmed: 32667913
doi: 10.1371/journal.pntd.0008459
pii: PNTD-D-19-01648
pmc: PMC7363076
doi:
Substances chimiques
Antigens, Viral
0
Rabies Vaccines
0
Vaccines, Synthetic
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
e0008459Subventions
Organisme : Medical Research Council
ID : MR/R010307/1
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/S009434/1
Pays : United Kingdom
Organisme : Biotechnology and Biological Sciences Research Council
ID : BB/J014508/1
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/R010307/1
Pays : United Kingdom
Commentaires et corrections
Type : ErratumIn
Déclaration de conflit d'intérêts
Benjamin Wizel is an employee of the GSK group of companies.
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