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Long-Term Immunogenicity and Efficacy of the Oral Rabies Virus Vaccine Strain SPBN GASGAS in Foxes
To evaluate the long-term immunogenicity of the live-attenuated, oral rabies vaccine SPBN GASGAS in a full good clinical practice (GCP) compliant study, forty-six (46) healthy, seronegative red foxes (Vulpes vulpes) were allocated to two treatment groups: group 1 (n = 31) received a vaccine bait con...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6784248/ https://www.ncbi.nlm.nih.gov/pubmed/31461981 http://dx.doi.org/10.3390/v11090790 |
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author | Freuling, Conrad M. te Kamp, Verena Klein, Antonia Günther, Maria Zaeck, Luca Potratz, Madlin Eggerbauer, Elisa Bobe, Katharina Kaiser, Christian Kretzschmar, Antje Ortmann, Steffen Schuster, Peter Vos, Adriaan Finke, Stefan Müller, Thomas |
author_facet | Freuling, Conrad M. te Kamp, Verena Klein, Antonia Günther, Maria Zaeck, Luca Potratz, Madlin Eggerbauer, Elisa Bobe, Katharina Kaiser, Christian Kretzschmar, Antje Ortmann, Steffen Schuster, Peter Vos, Adriaan Finke, Stefan Müller, Thomas |
author_sort | Freuling, Conrad M. |
collection | PubMed |
description | To evaluate the long-term immunogenicity of the live-attenuated, oral rabies vaccine SPBN GASGAS in a full good clinical practice (GCP) compliant study, forty-six (46) healthy, seronegative red foxes (Vulpes vulpes) were allocated to two treatment groups: group 1 (n = 31) received a vaccine bait containing 1.7 ml of the vaccine of minimum potency (10(6.6) FFU/mL) and group 2 (n = 15) received a placebo-bait. In total, 29 animals of group 1 and 14 animals of group 2 were challenged at 12 months post-vaccination with a fox rabies virus isolate (10(3.0) MICLD(50)/mL). While 90% of the animals offered a vaccine bait resisted the challenge, only one animal (7%) of the controls survived. All animals that had seroconverted following vaccination survived the challenge infection at 12 months post-vaccination. Rabies specific antibodies could be detected as early as 14 days post-vaccination. Based on the kinetics of the antibody response to SPBN GASGAS as measured in ELISA and RFFIT, the animals maintained stable antibody titres during the 12-month pre-challenge observation period at a high level. The results indicate that successful vaccination using the oral route with this new rabies virus vaccine strain confers long-term duration of immunity beyond one year, meeting the same requirements as for licensure as laid down by the European Pharmacopoeia. |
format | Online Article Text |
id | pubmed-6784248 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-67842482019-10-16 Long-Term Immunogenicity and Efficacy of the Oral Rabies Virus Vaccine Strain SPBN GASGAS in Foxes Freuling, Conrad M. te Kamp, Verena Klein, Antonia Günther, Maria Zaeck, Luca Potratz, Madlin Eggerbauer, Elisa Bobe, Katharina Kaiser, Christian Kretzschmar, Antje Ortmann, Steffen Schuster, Peter Vos, Adriaan Finke, Stefan Müller, Thomas Viruses Article To evaluate the long-term immunogenicity of the live-attenuated, oral rabies vaccine SPBN GASGAS in a full good clinical practice (GCP) compliant study, forty-six (46) healthy, seronegative red foxes (Vulpes vulpes) were allocated to two treatment groups: group 1 (n = 31) received a vaccine bait containing 1.7 ml of the vaccine of minimum potency (10(6.6) FFU/mL) and group 2 (n = 15) received a placebo-bait. In total, 29 animals of group 1 and 14 animals of group 2 were challenged at 12 months post-vaccination with a fox rabies virus isolate (10(3.0) MICLD(50)/mL). While 90% of the animals offered a vaccine bait resisted the challenge, only one animal (7%) of the controls survived. All animals that had seroconverted following vaccination survived the challenge infection at 12 months post-vaccination. Rabies specific antibodies could be detected as early as 14 days post-vaccination. Based on the kinetics of the antibody response to SPBN GASGAS as measured in ELISA and RFFIT, the animals maintained stable antibody titres during the 12-month pre-challenge observation period at a high level. The results indicate that successful vaccination using the oral route with this new rabies virus vaccine strain confers long-term duration of immunity beyond one year, meeting the same requirements as for licensure as laid down by the European Pharmacopoeia. MDPI 2019-08-27 /pmc/articles/PMC6784248/ /pubmed/31461981 http://dx.doi.org/10.3390/v11090790 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Freuling, Conrad M. te Kamp, Verena Klein, Antonia Günther, Maria Zaeck, Luca Potratz, Madlin Eggerbauer, Elisa Bobe, Katharina Kaiser, Christian Kretzschmar, Antje Ortmann, Steffen Schuster, Peter Vos, Adriaan Finke, Stefan Müller, Thomas Long-Term Immunogenicity and Efficacy of the Oral Rabies Virus Vaccine Strain SPBN GASGAS in Foxes |
title | Long-Term Immunogenicity and Efficacy of the Oral Rabies Virus Vaccine Strain SPBN GASGAS in Foxes |
title_full | Long-Term Immunogenicity and Efficacy of the Oral Rabies Virus Vaccine Strain SPBN GASGAS in Foxes |
title_fullStr | Long-Term Immunogenicity and Efficacy of the Oral Rabies Virus Vaccine Strain SPBN GASGAS in Foxes |
title_full_unstemmed | Long-Term Immunogenicity and Efficacy of the Oral Rabies Virus Vaccine Strain SPBN GASGAS in Foxes |
title_short | Long-Term Immunogenicity and Efficacy of the Oral Rabies Virus Vaccine Strain SPBN GASGAS in Foxes |
title_sort | long-term immunogenicity and efficacy of the oral rabies virus vaccine strain spbn gasgas in foxes |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6784248/ https://www.ncbi.nlm.nih.gov/pubmed/31461981 http://dx.doi.org/10.3390/v11090790 |
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