TY - JOUR
T1 - A Hendra virus G glycoprotein subunit vaccine protects African green monkeys from Nipah virus challenge
AU - Bossart, Katharine N.
AU - Rockx, Barry
AU - Feldmann, Friederike
AU - Brining, Doug
AU - Scott, Dana
AU - LaCasse, Rachel
AU - Geisbert, Joan B.
AU - Feng, Yan Ru
AU - Chan, Yee Peng
AU - Hickey, Andrew C.
AU - Broder, Christopher C.
AU - Feldmann, Heinz
AU - Geisbert, Thomas W.
PY - 2012/8/8
Y1 - 2012/8/8
N2 - In the 1990s, Hendra virus and Nipah virus (NiV), two closely related and previously unrecognized paramyxoviruses that cause severe disease and death in humans and a variety of animals, were discovered in Australia and Malaysia, respectively. Outbreaks of disease have occurred nearly every year since NiV was first discovered, with case fatality ranging from 10 to 100%. In the African green monkey (AGM), NiV causes a severe lethal respiratory and/or neurological disease that essentially mirrors fatal human disease. Thus, the AGM represents a reliable disease model for vaccine and therapeutic efficacy testing. We show that vaccination of AGMs with a recombinant subunit vaccine based on the henipavirus attachment G glycoprotein affords complete protection against subsequent NiV infection with no evidence of clinical disease, virus replication, or pathology observed in any challenged subjects. Success of the recombinant subunit vaccine in nonhuman primates provides crucial data in supporting its further preclinical development for potential human use.
AB - In the 1990s, Hendra virus and Nipah virus (NiV), two closely related and previously unrecognized paramyxoviruses that cause severe disease and death in humans and a variety of animals, were discovered in Australia and Malaysia, respectively. Outbreaks of disease have occurred nearly every year since NiV was first discovered, with case fatality ranging from 10 to 100%. In the African green monkey (AGM), NiV causes a severe lethal respiratory and/or neurological disease that essentially mirrors fatal human disease. Thus, the AGM represents a reliable disease model for vaccine and therapeutic efficacy testing. We show that vaccination of AGMs with a recombinant subunit vaccine based on the henipavirus attachment G glycoprotein affords complete protection against subsequent NiV infection with no evidence of clinical disease, virus replication, or pathology observed in any challenged subjects. Success of the recombinant subunit vaccine in nonhuman primates provides crucial data in supporting its further preclinical development for potential human use.
UR - http://www.scopus.com/inward/record.url?scp=84864851299&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84864851299&partnerID=8YFLogxK
U2 - 10.1126/scitranslmed.3004241
DO - 10.1126/scitranslmed.3004241
M3 - Article
C2 - 22875827
AN - SCOPUS:84864851299
SN - 1946-6234
VL - 4
JO - Science Translational Medicine
JF - Science Translational Medicine
IS - 146
M1 - 146ra107
ER -