Post-exposure therapy of filovirus infections

被引:54
作者
Wong, Gary [1 ,2 ]
Qiu, Xiangguo [1 ]
Olinger, Gene G. [3 ]
Kobinger, Gary P. [1 ,2 ,4 ,5 ]
机构
[1] Publ Hlth Agcy Canada, Natl Microbiol Lab, Special Pathogens Program, Winnipeg, MB, Canada
[2] Univ Manitoba, Dept Med Microbiol, Winnipeg, MB, Canada
[3] NIAID, Integrated Res Facil, NIH, Frederick, MD USA
[4] Univ Manitoba, Dept Immunol, Winnipeg, MB, Canada
[5] Univ Penn, Sch Med, Dept Pathol & Lab Med, Philadelphia, PA 19104 USA
关键词
filovirus; Ebola; Marburg; monoclonal antibodies; immunotherapy; post-exposure; ANTICOAGULANT PROTEIN C2; EBOLA HEMORRHAGIC-FEVER; NONHUMAN-PRIMATES; VESICULAR-STOMATITIS; MONOCLONAL-ANTIBODIES; VIRUS INFECTION; RHESUS-MONKEYS; MEDIATED PROTECTION; ZAIRE-EBOLAVIRUS; MARBURG VIRUSES;
D O I
10.1016/j.tim.2014.04.002
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Filovirus infections cause fatal hemorrhagic fever characterized by the initial onset of general symptoms before rapid progression to severe disease; the most virulent species can cause death to susceptible hosts within 10 days after the appearance of symptoms. Before the advent of monoclonal antibody (mAb) therapy, infection of non-human primates (NHPs) with the most virulent filovirus species was fatal if interventions were not administered within minutes. A novel nucleoside analogue, BCX4430, has since been shown to also demonstrate protective efficacy with a delayed treatment start. This review summarizes and evaluates the potential of current experimental candidates for treating filovirus disease with regard to their feasibility and use in the clinic, and assesses the most promising strategies towards the future development of a pan-filovirus medical countermeasure.
引用
收藏
页码:456 / 463
页数:8
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