| Literature DB >> 21987751 |
Stephan Günther1, Heinz Feldmann, Thomas W Geisbert, Lisa E Hensley, Pierre E Rollin, Stuart T Nichol, Ute Ströher, Harvey Artsob, Clarence J Peters, Thomas G Ksiazek, Stephan Becker, Jan ter Meulen, Stephan Olschläger, Jonas Schmidt-Chanasit, Hinrich Sudeck, Gerd D Burchard, Stefan Schmiedel.
Abstract
A needlestick injury occurred during an animal experiment in the biosafety level 4 laboratory in Hamburg, Germany, in March 2009. The syringe contained Zaire ebolavirus (ZEBOV) mixed with Freund's adjuvant. Neither an approved treatment nor a postexposure prophylaxis (PEP) exists for Ebola hemorrhagic fever. Following a risk-benefit assessment, it was recommended the exposed person take an experimental vaccine that had shown PEP efficacy in ZEBOV-infected nonhuman primates (NHPs) [12]. The vaccine, which had not been used previously in humans, was a live-attenuated recombinant vesicular stomatitis virus (recVSV) expressing the glycoprotein of ZEBOV. A single dose of 5 × 10(7) plaque-forming units was injected 48 hours after the accident. The vaccinee developed fever 12 hours later and recVSV viremia was detectable by polymerase chain reaction (PCR) for 2 days. Otherwise, the person remained healthy, and ZEBOV RNA, except for the glycoprotein gene expressed in the vaccine, was never detected in serum and peripheral blood mononuclear cells during the 3-week observation period.Entities:
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Year: 2011 PMID: 21987751 DOI: 10.1093/infdis/jir298
Source DB: PubMed Journal: J Infect Dis ISSN: 0022-1899 Impact factor: 5.226