Cargando…

Current status of vaccine development for tularemia preparedness

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 t...

Descripción completa

Detalles Bibliográficos
Autores principales: Hong, Kee-Jong, Park, Pil-Gu, Seo, Sang-Hwan, Rhie, Gi-eun, Hwang, Kyuh-Jam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Vaccine Society 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3623498/
https://www.ncbi.nlm.nih.gov/pubmed/23596588
http://dx.doi.org/10.7774/cevr.2013.2.1.34
_version_ 1782265923192750080
author Hong, Kee-Jong
Park, Pil-Gu
Seo, Sang-Hwan
Rhie, Gi-eun
Hwang, Kyuh-Jam
author_facet Hong, Kee-Jong
Park, Pil-Gu
Seo, Sang-Hwan
Rhie, Gi-eun
Hwang, Kyuh-Jam
author_sort Hong, Kee-Jong
collection PubMed
description 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.
format Online
Article
Text
id pubmed-3623498
institution National Center for Biotechnology Information
language English
publishDate 2013
publisher The Korean Vaccine Society
record_format MEDLINE/PubMed
spelling pubmed-36234982013-04-17 Current status of vaccine development for tularemia preparedness Hong, Kee-Jong Park, Pil-Gu Seo, Sang-Hwan Rhie, Gi-eun Hwang, Kyuh-Jam Clin Exp Vaccine Res Review Article 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. The Korean Vaccine Society 2013-01 2013-01-15 /pmc/articles/PMC3623498/ /pubmed/23596588 http://dx.doi.org/10.7774/cevr.2013.2.1.34 Text en © Korean Vaccine Society. http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Hong, Kee-Jong
Park, Pil-Gu
Seo, Sang-Hwan
Rhie, Gi-eun
Hwang, Kyuh-Jam
Current status of vaccine development for tularemia preparedness
title Current status of vaccine development for tularemia preparedness
title_full Current status of vaccine development for tularemia preparedness
title_fullStr Current status of vaccine development for tularemia preparedness
title_full_unstemmed Current status of vaccine development for tularemia preparedness
title_short Current status of vaccine development for tularemia preparedness
title_sort current status of vaccine development for tularemia preparedness
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3623498/
https://www.ncbi.nlm.nih.gov/pubmed/23596588
http://dx.doi.org/10.7774/cevr.2013.2.1.34
work_keys_str_mv AT hongkeejong currentstatusofvaccinedevelopmentfortularemiapreparedness
AT parkpilgu currentstatusofvaccinedevelopmentfortularemiapreparedness
AT seosanghwan currentstatusofvaccinedevelopmentfortularemiapreparedness
AT rhiegieun currentstatusofvaccinedevelopmentfortularemiapreparedness
AT hwangkyuhjam currentstatusofvaccinedevelopmentfortularemiapreparedness