Memory immune responses against pandemic (H1N1) 2009 influenza virus induced by a whole particle vaccine in cynomolgus monkeys carrying Mafa-A1*052:02.

We made an H1N1 vaccine candidate from a virus library consisting of 144 ( = 16 HA×9 NA) non-pathogenic influenza A viruses and examined its protective effects against a pandemic (2009) H1N1 strain using immunologically naïve cynomolgus macaques to exclude preexisting immunity and to employ a precli...

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Autores principales: Masahiko Arikata, Yasushi Itoh, Masatoshi Okamatsu, Toshinaga Maeda, Takashi Shiina, Keiko Tanaka, Shingo Suzuki, Misako Nakayama, Yoshihiro Sakoda, Hirohito Ishigaki, Ayato Takada, Hideaki Ishida, Kosuke Soda, Van Loi Pham, Hideaki Tsuchiya, Shinichiro Nakamura, Ryuzo Torii, Takeshi Shimizu, Hidetoshi Inoko, Iwao Ohkubo, Hiroshi Kida, Kazumasa Ogasawara
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Publicado: Public Library of Science (PLoS) 2012
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spelling oai:doaj.org-article:598b83786227441f893eae280be85bcf2021-11-18T07:18:11ZMemory immune responses against pandemic (H1N1) 2009 influenza virus induced by a whole particle vaccine in cynomolgus monkeys carrying Mafa-A1*052:02.1932-620310.1371/journal.pone.0037220https://doaj.org/article/598b83786227441f893eae280be85bcf2012-01-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/22623997/pdf/?tool=EBIhttps://doaj.org/toc/1932-6203We made an H1N1 vaccine candidate from a virus library consisting of 144 ( = 16 HA×9 NA) non-pathogenic influenza A viruses and examined its protective effects against a pandemic (2009) H1N1 strain using immunologically naïve cynomolgus macaques to exclude preexisting immunity and to employ a preclinical study since preexisting immunity in humans previously vaccinated or infected with influenza virus might make comparison of vaccine efficacy difficult. Furthermore, macaques carrying a major histocompatibility complex class I molecule, Mafa-A1*052:02, were used to analyze peptide-specific CD8(+) T cell responses. Sera of macaques immunized with an inactivated whole particle formulation without addition of an adjuvant showed higher neutralization titers against the vaccine strain A/Hokkaido/2/1981 (H1N1) than did sera of macaques immunized with a split formulation. Neutralization activities against the pandemic strain A/Narita/1/2009 (H1N1) in sera of macaques immunized twice with the split vaccine reached levels similar to those in sera of macaques immunized once with the whole particle vaccine. After inoculation with the pandemic virus, the virus was detected in nasal samples of unvaccinated macaques for 6 days after infection and for 2.67 days and 5.33 days on average in macaques vaccinated with the whole particle vaccine and the split vaccine, respectively. After the challenge infection, recall neutralizing antibody responses against the pandemic virus and CD8(+) T cell responses specific for nucleoprotein peptide NP262-270 bound to Mafa-A1*052:02 in macaques vaccinated with the whole particle vaccine were observed more promptly or more vigorously than those in macaques vaccinated with the split vaccine. These findings demonstrated that the vaccine derived from our virus library was effective for pandemic virus infection in macaques and that the whole particle vaccine conferred more effective memory and broader cross-reactive immune responses to macaques against pandemic influenza virus infection than did the split vaccine.Masahiko ArikataYasushi ItohMasatoshi OkamatsuToshinaga MaedaTakashi ShiinaKeiko TanakaShingo SuzukiMisako NakayamaYoshihiro SakodaHirohito IshigakiAyato TakadaHideaki IshidaKosuke SodaVan Loi PhamHideaki TsuchiyaShinichiro NakamuraRyuzo ToriiTakeshi ShimizuHidetoshi InokoIwao OhkuboHiroshi KidaKazumasa OgasawaraPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 7, Iss 5, p e37220 (2012)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Masahiko Arikata
Yasushi Itoh
Masatoshi Okamatsu
Toshinaga Maeda
Takashi Shiina
Keiko Tanaka
Shingo Suzuki
Misako Nakayama
Yoshihiro Sakoda
Hirohito Ishigaki
Ayato Takada
Hideaki Ishida
Kosuke Soda
Van Loi Pham
Hideaki Tsuchiya
Shinichiro Nakamura
Ryuzo Torii
Takeshi Shimizu
Hidetoshi Inoko
Iwao Ohkubo
Hiroshi Kida
Kazumasa Ogasawara
Memory immune responses against pandemic (H1N1) 2009 influenza virus induced by a whole particle vaccine in cynomolgus monkeys carrying Mafa-A1*052:02.
description We made an H1N1 vaccine candidate from a virus library consisting of 144 ( = 16 HA×9 NA) non-pathogenic influenza A viruses and examined its protective effects against a pandemic (2009) H1N1 strain using immunologically naïve cynomolgus macaques to exclude preexisting immunity and to employ a preclinical study since preexisting immunity in humans previously vaccinated or infected with influenza virus might make comparison of vaccine efficacy difficult. Furthermore, macaques carrying a major histocompatibility complex class I molecule, Mafa-A1*052:02, were used to analyze peptide-specific CD8(+) T cell responses. Sera of macaques immunized with an inactivated whole particle formulation without addition of an adjuvant showed higher neutralization titers against the vaccine strain A/Hokkaido/2/1981 (H1N1) than did sera of macaques immunized with a split formulation. Neutralization activities against the pandemic strain A/Narita/1/2009 (H1N1) in sera of macaques immunized twice with the split vaccine reached levels similar to those in sera of macaques immunized once with the whole particle vaccine. After inoculation with the pandemic virus, the virus was detected in nasal samples of unvaccinated macaques for 6 days after infection and for 2.67 days and 5.33 days on average in macaques vaccinated with the whole particle vaccine and the split vaccine, respectively. After the challenge infection, recall neutralizing antibody responses against the pandemic virus and CD8(+) T cell responses specific for nucleoprotein peptide NP262-270 bound to Mafa-A1*052:02 in macaques vaccinated with the whole particle vaccine were observed more promptly or more vigorously than those in macaques vaccinated with the split vaccine. These findings demonstrated that the vaccine derived from our virus library was effective for pandemic virus infection in macaques and that the whole particle vaccine conferred more effective memory and broader cross-reactive immune responses to macaques against pandemic influenza virus infection than did the split vaccine.
format article
author Masahiko Arikata
Yasushi Itoh
Masatoshi Okamatsu
Toshinaga Maeda
Takashi Shiina
Keiko Tanaka
Shingo Suzuki
Misako Nakayama
Yoshihiro Sakoda
Hirohito Ishigaki
Ayato Takada
Hideaki Ishida
Kosuke Soda
Van Loi Pham
Hideaki Tsuchiya
Shinichiro Nakamura
Ryuzo Torii
Takeshi Shimizu
Hidetoshi Inoko
Iwao Ohkubo
Hiroshi Kida
Kazumasa Ogasawara
author_facet Masahiko Arikata
Yasushi Itoh
Masatoshi Okamatsu
Toshinaga Maeda
Takashi Shiina
Keiko Tanaka
Shingo Suzuki
Misako Nakayama
Yoshihiro Sakoda
Hirohito Ishigaki
Ayato Takada
Hideaki Ishida
Kosuke Soda
Van Loi Pham
Hideaki Tsuchiya
Shinichiro Nakamura
Ryuzo Torii
Takeshi Shimizu
Hidetoshi Inoko
Iwao Ohkubo
Hiroshi Kida
Kazumasa Ogasawara
author_sort Masahiko Arikata
title Memory immune responses against pandemic (H1N1) 2009 influenza virus induced by a whole particle vaccine in cynomolgus monkeys carrying Mafa-A1*052:02.
title_short Memory immune responses against pandemic (H1N1) 2009 influenza virus induced by a whole particle vaccine in cynomolgus monkeys carrying Mafa-A1*052:02.
title_full Memory immune responses against pandemic (H1N1) 2009 influenza virus induced by a whole particle vaccine in cynomolgus monkeys carrying Mafa-A1*052:02.
title_fullStr Memory immune responses against pandemic (H1N1) 2009 influenza virus induced by a whole particle vaccine in cynomolgus monkeys carrying Mafa-A1*052:02.
title_full_unstemmed Memory immune responses against pandemic (H1N1) 2009 influenza virus induced by a whole particle vaccine in cynomolgus monkeys carrying Mafa-A1*052:02.
title_sort memory immune responses against pandemic (h1n1) 2009 influenza virus induced by a whole particle vaccine in cynomolgus monkeys carrying mafa-a1*052:02.
publisher Public Library of Science (PLoS)
publishDate 2012
url https://doaj.org/article/598b83786227441f893eae280be85bcf
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