TY - JOUR
T1 - A next generation vaccine against human rabies based on a single dose of a chimpanzee adenovirus vector serotype c
AU - Napolitano, Federico
AU - Merone, Rossella
AU - Abbate, Adele
AU - Ammendola, Virginia
AU - Horncastle, Emma
AU - Lanzaro, Francesca
AU - Esposito, Marialuisa
AU - Contino, Alessandra Maria
AU - Sbrocchi, Roberta
AU - Sommella, Andrea
AU - Duncan, Joshua D.
AU - Hinds, Jospeh
AU - Urbanowicz, Richard A.
AU - Lahm, Armin
AU - Colloca, Stefano
AU - Folgori, Antonella
AU - Ball, Jonathan
AU - Nicosia, Alfredo
AU - Wizel, Benjamin
AU - Capone, Stefania
AU - Vitelli, Alessandra
PY - 2020/7/15
Y1 - 2020/7/15
N2 - 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 sched-ule, 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 ade-novirus 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 expo-sure. 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.
AB - 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 sched-ule, 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 ade-novirus 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 expo-sure. 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.
U2 - 10.1371/journal.pntd.0008459
DO - 10.1371/journal.pntd.0008459
M3 - Article
SN - 1935-2727
VL - 14
SP - 1
EP - 26
JO - PLoS Neglected Tropical Diseases
JF - PLoS Neglected Tropical Diseases
IS - 7
M1 - e0008459
ER -