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Serological Correlate of Protection in Guinea Pigs for a Recombinant Protective Antigen Anthrax Vaccine Produced from Bacillus brevis

OBJECTIVE: Recombinant protective antigen (rPA) is the active pharmaceutical ingredient of a second generation anthrax vaccine undergoing clinical trials both in Korea and the USA. By using the rPA produced from Bacillus brevis pNU212 expression system, correlations of serological immune response to...

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Autores principales: Chun, Jeong-Hoon, Choi, On-Jee, Cho, Min-Hee, Hong, Kee-Jong, Seong, Won Keun, Oh, Hee-Bok, Rhie, Gi-Eun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korea Centers for Disease Control and Prevention 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3738701/
https://www.ncbi.nlm.nih.gov/pubmed/24159510
http://dx.doi.org/10.1016/j.phrp.2012.07.006
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author Chun, Jeong-Hoon
Choi, On-Jee
Cho, Min-Hee
Hong, Kee-Jong
Seong, Won Keun
Oh, Hee-Bok
Rhie, Gi-Eun
author_facet Chun, Jeong-Hoon
Choi, On-Jee
Cho, Min-Hee
Hong, Kee-Jong
Seong, Won Keun
Oh, Hee-Bok
Rhie, Gi-Eun
author_sort Chun, Jeong-Hoon
collection PubMed
description OBJECTIVE: Recombinant protective antigen (rPA) is the active pharmaceutical ingredient of a second generation anthrax vaccine undergoing clinical trials both in Korea and the USA. By using the rPA produced from Bacillus brevis pNU212 expression system, correlations of serological immune response to anthrax protection efficacy were analyzed in a guinea pig model. METHODS: Serological responses of rPA anthrax vaccine were investigated in guinea pigs that were given single or two injections (interval of 4 weeks) of various amounts of rPA combined with aluminumhydroxide adjuvant. Guinea pigs were subsequently challenged by the intramuscular injection with 30 half-lethal doses (30LD(50)) of virulent Bacillus anthracis spores. Serumantibody titerswere determined by anti-PA IgGELISA and the ability of antibodies to neutralize the cytotoxicity of lethal toxin on J774A.1 cell was measured through the toxin neutralizing antibody (TNA) assay. RESULTS: To examine correlations between survival rate and antibody titers, correlation between neutralizing antibody titers and the extent of protection was determined. Toxin neutralization titers of at least 1176 were sufficient to confer protection against a dose of 30LD(50) of virulent anthrax spores of the H9401 strain. Such consistency in the correlation was not observed from those antibody titers determined by ELISA. CONCLUSION: Neutralizing-antibody titers can be used as a surrogate marker.
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spelling pubmed-37387012013-10-24 Serological Correlate of Protection in Guinea Pigs for a Recombinant Protective Antigen Anthrax Vaccine Produced from Bacillus brevis Chun, Jeong-Hoon Choi, On-Jee Cho, Min-Hee Hong, Kee-Jong Seong, Won Keun Oh, Hee-Bok Rhie, Gi-Eun Osong Public Health Res Perspect Articles OBJECTIVE: Recombinant protective antigen (rPA) is the active pharmaceutical ingredient of a second generation anthrax vaccine undergoing clinical trials both in Korea and the USA. By using the rPA produced from Bacillus brevis pNU212 expression system, correlations of serological immune response to anthrax protection efficacy were analyzed in a guinea pig model. METHODS: Serological responses of rPA anthrax vaccine were investigated in guinea pigs that were given single or two injections (interval of 4 weeks) of various amounts of rPA combined with aluminumhydroxide adjuvant. Guinea pigs were subsequently challenged by the intramuscular injection with 30 half-lethal doses (30LD(50)) of virulent Bacillus anthracis spores. Serumantibody titerswere determined by anti-PA IgGELISA and the ability of antibodies to neutralize the cytotoxicity of lethal toxin on J774A.1 cell was measured through the toxin neutralizing antibody (TNA) assay. RESULTS: To examine correlations between survival rate and antibody titers, correlation between neutralizing antibody titers and the extent of protection was determined. Toxin neutralization titers of at least 1176 were sufficient to confer protection against a dose of 30LD(50) of virulent anthrax spores of the H9401 strain. Such consistency in the correlation was not observed from those antibody titers determined by ELISA. CONCLUSION: Neutralizing-antibody titers can be used as a surrogate marker. Korea Centers for Disease Control and Prevention 2012-09 /pmc/articles/PMC3738701/ /pubmed/24159510 http://dx.doi.org/10.1016/j.phrp.2012.07.006 Text en Copyright ©2012, Korea Centers for Disease Control and Prevention 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 Articles
Chun, Jeong-Hoon
Choi, On-Jee
Cho, Min-Hee
Hong, Kee-Jong
Seong, Won Keun
Oh, Hee-Bok
Rhie, Gi-Eun
Serological Correlate of Protection in Guinea Pigs for a Recombinant Protective Antigen Anthrax Vaccine Produced from Bacillus brevis
title Serological Correlate of Protection in Guinea Pigs for a Recombinant Protective Antigen Anthrax Vaccine Produced from Bacillus brevis
title_full Serological Correlate of Protection in Guinea Pigs for a Recombinant Protective Antigen Anthrax Vaccine Produced from Bacillus brevis
title_fullStr Serological Correlate of Protection in Guinea Pigs for a Recombinant Protective Antigen Anthrax Vaccine Produced from Bacillus brevis
title_full_unstemmed Serological Correlate of Protection in Guinea Pigs for a Recombinant Protective Antigen Anthrax Vaccine Produced from Bacillus brevis
title_short Serological Correlate of Protection in Guinea Pigs for a Recombinant Protective Antigen Anthrax Vaccine Produced from Bacillus brevis
title_sort serological correlate of protection in guinea pigs for a recombinant protective antigen anthrax vaccine produced from bacillus brevis
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3738701/
https://www.ncbi.nlm.nih.gov/pubmed/24159510
http://dx.doi.org/10.1016/j.phrp.2012.07.006
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