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Safety testing of acellular pertussis vaccines: Use of animals and 3Rs alternatives

The current test of acellular Bordetella pertussis (aP) vaccines for residual pertussis toxin (PTx) is the Histamine Sensitization test (HIST), based on the empirical finding that PTx sensitizes mice to histamine. Although HIST has ensured the safety of aP vaccines for years, it is criticized for th...

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Autores principales: Hoonakker, Marieke, Arciniega, Juan, Hendriksen, Coenraad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5703371/
https://www.ncbi.nlm.nih.gov/pubmed/28857652
http://dx.doi.org/10.1080/21645515.2017.1349585
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author Hoonakker, Marieke
Arciniega, Juan
Hendriksen, Coenraad
author_facet Hoonakker, Marieke
Arciniega, Juan
Hendriksen, Coenraad
author_sort Hoonakker, Marieke
collection PubMed
description The current test of acellular Bordetella pertussis (aP) vaccines for residual pertussis toxin (PTx) is the Histamine Sensitization test (HIST), based on the empirical finding that PTx sensitizes mice to histamine. Although HIST has ensured the safety of aP vaccines for years, it is criticized for the limited understanding of how it works, its technical difficulty, and for animal welfare reasons. To estimate the number of mice used worldwide for HIST, we surveyed major aP manufacturers and organizations performing, requiring, or recommending the test. The survey revealed marked regional differences in regulatory guidelines, including the number of animals used for a single test. Based on information provided by the parties surveyed, we estimated the worldwide number of mice used for testing to be 65,000 per year: ∼48,000 by manufacturers and ∼17,000 by national control laboratories, although the latter number is more affected by uncertainty, due to confidentiality policies. These animals covered the release of approximately 850 final lots and 250 in-process lots of aP vaccines yearly. Although there are several approaches for HIST refinement and reduction, we discuss why the efforts needed for validation and implementation of these interim alternatives may not be worthwhile, when there are several in vitro alternatives in various stages of development, some already fairly advanced. Upon implementation, one or more of these replacement alternatives can substantially reduce the number of animals currently used for the HIST, although careful evaluation of each alternative's mechanism and its suitable validation will be necessary in the path to implementation.
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spelling pubmed-57033712017-12-04 Safety testing of acellular pertussis vaccines: Use of animals and 3Rs alternatives Hoonakker, Marieke Arciniega, Juan Hendriksen, Coenraad Hum Vaccin Immunother Review The current test of acellular Bordetella pertussis (aP) vaccines for residual pertussis toxin (PTx) is the Histamine Sensitization test (HIST), based on the empirical finding that PTx sensitizes mice to histamine. Although HIST has ensured the safety of aP vaccines for years, it is criticized for the limited understanding of how it works, its technical difficulty, and for animal welfare reasons. To estimate the number of mice used worldwide for HIST, we surveyed major aP manufacturers and organizations performing, requiring, or recommending the test. The survey revealed marked regional differences in regulatory guidelines, including the number of animals used for a single test. Based on information provided by the parties surveyed, we estimated the worldwide number of mice used for testing to be 65,000 per year: ∼48,000 by manufacturers and ∼17,000 by national control laboratories, although the latter number is more affected by uncertainty, due to confidentiality policies. These animals covered the release of approximately 850 final lots and 250 in-process lots of aP vaccines yearly. Although there are several approaches for HIST refinement and reduction, we discuss why the efforts needed for validation and implementation of these interim alternatives may not be worthwhile, when there are several in vitro alternatives in various stages of development, some already fairly advanced. Upon implementation, one or more of these replacement alternatives can substantially reduce the number of animals currently used for the HIST, although careful evaluation of each alternative's mechanism and its suitable validation will be necessary in the path to implementation. Taylor & Francis 2017-08-31 /pmc/articles/PMC5703371/ /pubmed/28857652 http://dx.doi.org/10.1080/21645515.2017.1349585 Text en © 2017 Intravacc. Published with license by Taylor & Francis http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited, and is not altered, transformed, or built upon in any way.
spellingShingle Review
Hoonakker, Marieke
Arciniega, Juan
Hendriksen, Coenraad
Safety testing of acellular pertussis vaccines: Use of animals and 3Rs alternatives
title Safety testing of acellular pertussis vaccines: Use of animals and 3Rs alternatives
title_full Safety testing of acellular pertussis vaccines: Use of animals and 3Rs alternatives
title_fullStr Safety testing of acellular pertussis vaccines: Use of animals and 3Rs alternatives
title_full_unstemmed Safety testing of acellular pertussis vaccines: Use of animals and 3Rs alternatives
title_short Safety testing of acellular pertussis vaccines: Use of animals and 3Rs alternatives
title_sort safety testing of acellular pertussis vaccines: use of animals and 3rs alternatives
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5703371/
https://www.ncbi.nlm.nih.gov/pubmed/28857652
http://dx.doi.org/10.1080/21645515.2017.1349585
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