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CLINICAL and EXPERIMENTAL VACCINE RESEARCH
  • Date2018-02-05 16:19
  • Update2018-02-05 16:32
  • CountersignatureDivision of Research Planning
  • Tel043-719-8033
Current status of vaccine development for tularemia preparedness development for tularemia preparedness, 2013, 02, 34─39

CLINICAL and EXPERIMENTAL VACCINE RESEARCH

Kee-jong Hong, Pil-Gu Park, Sang-Hwan Seo, Gi-eun Rhie, Kyuh-Jam Hwang

Abstract

    Tularemia is a high-risk infectious disease caused by Gram-negative bacterium Francisella tularensis. Due to its high fatality at very low colony-forming units (less than 10), F. tularensis is considered as a powerful potential bioterrorism agent. Vaccine could be the most efficient way to prevent the citizen from infection of F. tularensis when the bioterrorism happens, but officially approved vaccine with both efficacy and safety is not developed yet. Research for the development of tularemia vaccine has been focusing on the live attenuated vaccine strain (LVS) for long history, still there are no LVS confirmed for the safety which should be an essential factor for general vaccination program. Furthermore the LVS did not show protection efficacy against high-risk subspecies tularensis (type A) as high as the level against subspecies holarctica (type B) in human. Though the subunit or recombinant vaccine candidates have been considered for better safety, any results did not show better prevention efficacy than the LVS candidate against F. tularensis infection. Currently there are some more trials to develop vaccine using mutant strains or nonpathogenic F. novicida strain, but it did not reveal effective candidates overwhelming the LVS either. Difference in the protection efficacy of LVS against type A strain in human and the low level protection of many subunit or recombinant vaccine candidates lead the scientists to consider the live vaccine development using type A strain could be ultimate answer for the tularemia vaccine development.


  • ISBN or ISSN: 2287-3651

  • 본 연구는 질병관리본부 연구개발과제(과제번호 2013-NG45001-00) 연구비를 지원받아 수행되었습니다.
  • This research was supported by a fund(code 2013-NG45001-00) by Research of Korea Centers for Disease Control and Prevention.


This public work may be used under the terms of the public interest source + commercial use prohibition + nonrepudiation conditions This public work may be used under the terms of the public interest source + commercial use prohibition + nonrepudiation conditions
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