A whole virus pandemic influenza H1N1 vaccine is highly immunogenic and protective in active immunization and passive protection mouse models.

The recent emergence and rapid spread of a novel swine-derived H1N1 influenza virus has resulted in the first influenza pandemic of this century. Monovalent vaccines have undergone preclinical and clinical development prior to initiation of mass immunization campaigns. We have carried out a series o...

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Autores principales: Otfried Kistner, Brian A Crowe, Walter Wodal, Astrid Kerschbaum, Helga Savidis-Dacho, Nicolas Sabarth, Falko G Falkner, Ines Mayerhofer, Wolfgang Mundt, Manfred Reiter, Leopold Grillberger, Christa Tauer, Michael Graninger, Alois Sachslehner, Michael Schwendinger, Peter Brühl, Thomas R Kreil, Hartmut J Ehrlich, P Noel Barrett
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Publicado: Public Library of Science (PLoS) 2010
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spelling oai:doaj.org-article:371cf088181640879869f94a514c85ae2021-11-25T06:25:38ZA whole virus pandemic influenza H1N1 vaccine is highly immunogenic and protective in active immunization and passive protection mouse models.1932-620310.1371/journal.pone.0009349https://doaj.org/article/371cf088181640879869f94a514c85ae2010-02-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/20186321/?tool=EBIhttps://doaj.org/toc/1932-6203The recent emergence and rapid spread of a novel swine-derived H1N1 influenza virus has resulted in the first influenza pandemic of this century. Monovalent vaccines have undergone preclinical and clinical development prior to initiation of mass immunization campaigns. We have carried out a series of immunogenicity and protection studies following active immunization of mice, which indicate that a whole virus, nonadjuvanted vaccine is immunogenic at low doses and protects against live virus challenge. The immunogenicity in this model was comparable to that of a whole virus H5N1 vaccine, which had previously been demonstrated to induce high levels of seroprotection in clinical studies. The efficacy of the H1N1 pandemic vaccine in protecting against live virus challenge was also seen to be equivalent to that of the H5N1 vaccine. The protective efficacy of the H1N1 vaccine was also confirmed using a severe combined immunodeficient (SCID) mouse model. It was demonstrated that mouse and guinea pig immune sera elicited following active H1N1 vaccination resulted in 100% protection of SCID mice following passive transfer of immune sera and lethal challenge. The immune responses to a whole virus pandemic H1N1 and a split seasonal H1N1 vaccine were also compared in this study. It was demonstrated that the whole virus vaccine induced a balanced Th-1 and Th-2 response in mice, whereas the split vaccine induced mainly a Th-2 response and only minimal levels of Th-1 responses. These data supported the initiation of clinical studies with the same low doses of whole virus vaccine that had previously been demonstrated to be immunogenic in clinical studies with a whole virus H5N1 vaccine.Otfried KistnerBrian A CroweWalter WodalAstrid KerschbaumHelga Savidis-DachoNicolas SabarthFalko G FalknerInes MayerhoferWolfgang MundtManfred ReiterLeopold GrillbergerChrista TauerMichael GraningerAlois SachslehnerMichael SchwendingerPeter BrühlThomas R KreilHartmut J EhrlichP Noel BarrettPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 5, Iss 2, p e9349 (2010)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Otfried Kistner
Brian A Crowe
Walter Wodal
Astrid Kerschbaum
Helga Savidis-Dacho
Nicolas Sabarth
Falko G Falkner
Ines Mayerhofer
Wolfgang Mundt
Manfred Reiter
Leopold Grillberger
Christa Tauer
Michael Graninger
Alois Sachslehner
Michael Schwendinger
Peter Brühl
Thomas R Kreil
Hartmut J Ehrlich
P Noel Barrett
A whole virus pandemic influenza H1N1 vaccine is highly immunogenic and protective in active immunization and passive protection mouse models.
description The recent emergence and rapid spread of a novel swine-derived H1N1 influenza virus has resulted in the first influenza pandemic of this century. Monovalent vaccines have undergone preclinical and clinical development prior to initiation of mass immunization campaigns. We have carried out a series of immunogenicity and protection studies following active immunization of mice, which indicate that a whole virus, nonadjuvanted vaccine is immunogenic at low doses and protects against live virus challenge. The immunogenicity in this model was comparable to that of a whole virus H5N1 vaccine, which had previously been demonstrated to induce high levels of seroprotection in clinical studies. The efficacy of the H1N1 pandemic vaccine in protecting against live virus challenge was also seen to be equivalent to that of the H5N1 vaccine. The protective efficacy of the H1N1 vaccine was also confirmed using a severe combined immunodeficient (SCID) mouse model. It was demonstrated that mouse and guinea pig immune sera elicited following active H1N1 vaccination resulted in 100% protection of SCID mice following passive transfer of immune sera and lethal challenge. The immune responses to a whole virus pandemic H1N1 and a split seasonal H1N1 vaccine were also compared in this study. It was demonstrated that the whole virus vaccine induced a balanced Th-1 and Th-2 response in mice, whereas the split vaccine induced mainly a Th-2 response and only minimal levels of Th-1 responses. These data supported the initiation of clinical studies with the same low doses of whole virus vaccine that had previously been demonstrated to be immunogenic in clinical studies with a whole virus H5N1 vaccine.
format article
author Otfried Kistner
Brian A Crowe
Walter Wodal
Astrid Kerschbaum
Helga Savidis-Dacho
Nicolas Sabarth
Falko G Falkner
Ines Mayerhofer
Wolfgang Mundt
Manfred Reiter
Leopold Grillberger
Christa Tauer
Michael Graninger
Alois Sachslehner
Michael Schwendinger
Peter Brühl
Thomas R Kreil
Hartmut J Ehrlich
P Noel Barrett
author_facet Otfried Kistner
Brian A Crowe
Walter Wodal
Astrid Kerschbaum
Helga Savidis-Dacho
Nicolas Sabarth
Falko G Falkner
Ines Mayerhofer
Wolfgang Mundt
Manfred Reiter
Leopold Grillberger
Christa Tauer
Michael Graninger
Alois Sachslehner
Michael Schwendinger
Peter Brühl
Thomas R Kreil
Hartmut J Ehrlich
P Noel Barrett
author_sort Otfried Kistner
title A whole virus pandemic influenza H1N1 vaccine is highly immunogenic and protective in active immunization and passive protection mouse models.
title_short A whole virus pandemic influenza H1N1 vaccine is highly immunogenic and protective in active immunization and passive protection mouse models.
title_full A whole virus pandemic influenza H1N1 vaccine is highly immunogenic and protective in active immunization and passive protection mouse models.
title_fullStr A whole virus pandemic influenza H1N1 vaccine is highly immunogenic and protective in active immunization and passive protection mouse models.
title_full_unstemmed A whole virus pandemic influenza H1N1 vaccine is highly immunogenic and protective in active immunization and passive protection mouse models.
title_sort whole virus pandemic influenza h1n1 vaccine is highly immunogenic and protective in active immunization and passive protection mouse models.
publisher Public Library of Science (PLoS)
publishDate 2010
url https://doaj.org/article/371cf088181640879869f94a514c85ae
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