Management of Accidental Exposure to Ebola Virus in the Biosafety Level 4 Laboratory, Hamburg, Germany

被引:113
作者
Guenther, Stephan [1 ]
Feldmann, Heinz [2 ]
Geisbert, Thomas W. [3 ]
Hensley, Lisa E. [4 ]
Rollin, Pierre E. [5 ]
Nichol, Stuart T. [5 ]
Stroeher, Ute [6 ]
Artsob, Harvey [6 ]
Peters, Clarence J. [7 ]
Ksiazek, Thomas G. [8 ]
Becker, Stephan [9 ]
ter Meulen, Jan [10 ]
Oelschlaeger, Stephan [1 ]
Schmidt-Chanasit, Jonas [1 ]
Sudeck, Hinrich [11 ]
Burchard, Gerd D. [12 ]
Schmiedel, Stefan [12 ]
机构
[1] Bernhard Nocht Inst Trop Med, Dept Virol, D-20359 Hamburg, Germany
[2] NIAID, Virol Lab, Div Intramural Res, NIH, Hamilton, MT USA
[3] Boston Univ, Sch Med, Natl Emerging Infect Dis Labs Inst, Boston, MA 02118 USA
[4] USA, Med Res Inst Infect Dis, Ft Detrick, MD 21702 USA
[5] Ctr Dis Control & Prevent, Viral Special Pathogens Branch, Div High Consequence Pathogens & Pathol, Atlanta, GA USA
[6] Publ Hlth Agcy Canada, Special Pathogens Program, Natl Microbiol Lab, Winnipeg, MB, Canada
[7] Univ Texas Med Branch, Ctr Biodef & Emerging Infect Dis, Galveston, TX USA
[8] Univ Texas Med Branch, Galveston Natl Lab, Dept Pathol, Galveston, TX USA
[9] Univ Marburg, Inst Virol, D-35032 Marburg, Germany
[10] Merck Res Labs, Vaccine Res, West Point, PA USA
[11] Bundeswehrkrankenhaus Hamburg, Hamburg, Germany
[12] Univ Med Ctr Hamburg Eppendorf, Hamburg, Germany
关键词
VESICULAR-STOMATITIS-VIRUS; HEMORRHAGIC-FEVER; NONHUMAN-PRIMATES; POSTEXPOSURE PROTECTION; RISK-FACTORS; INFECTION; TRANSMISSION; INTERFERON; SUDAN; 1-BETA-D-RIBOFURANOSYL-1,2,4-TRIAZOLE-3-CARBOXAMIDE;
D O I
10.1093/infdis/jir298
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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 x 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.
引用
收藏
页码:S785 / S790
页数:6
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