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Immune Protection Induced on Day 10 Following Administration of the 2009 A/H1N1 Pandemic Influenza Vaccine

BACKGROUND: The 2009 swine-origin influenza virus (S-OIV) H1N1 pandemic has caused more than 18,000 deaths worldwide. Vaccines against the 2009 A/H1N1 influenza virus are useful for preventing infection and controlling the pandemic. The kinetics of the immune response following vaccination with the...

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Autores principales: Sun, Yizhuo, Bian, Chao, Xu, Ke, Hu, Weibin, Wang, Tongyan, Cui, Jun, Wu, Hongqiang, Ling, Zhiyang, Ji, Yongyong, Lin, Guomei, Tian, Lin, Zhou, Yanyan, Li, Bingnan, Hu, Guiyu, Yu, Ning, An, Wenqi, Pan, Ruowen, Zhou, Paul, Leng, Qibin, Huang, Zhong, Ma, Xiaowei, Sun, Bing
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3000335/
https://www.ncbi.nlm.nih.gov/pubmed/21151563
http://dx.doi.org/10.1371/journal.pone.0014270
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author Sun, Yizhuo
Bian, Chao
Xu, Ke
Hu, Weibin
Wang, Tongyan
Cui, Jun
Wu, Hongqiang
Ling, Zhiyang
Ji, Yongyong
Lin, Guomei
Tian, Lin
Zhou, Yanyan
Li, Bingnan
Hu, Guiyu
Yu, Ning
An, Wenqi
Pan, Ruowen
Zhou, Paul
Leng, Qibin
Huang, Zhong
Ma, Xiaowei
Sun, Bing
author_facet Sun, Yizhuo
Bian, Chao
Xu, Ke
Hu, Weibin
Wang, Tongyan
Cui, Jun
Wu, Hongqiang
Ling, Zhiyang
Ji, Yongyong
Lin, Guomei
Tian, Lin
Zhou, Yanyan
Li, Bingnan
Hu, Guiyu
Yu, Ning
An, Wenqi
Pan, Ruowen
Zhou, Paul
Leng, Qibin
Huang, Zhong
Ma, Xiaowei
Sun, Bing
author_sort Sun, Yizhuo
collection PubMed
description BACKGROUND: The 2009 swine-origin influenza virus (S-OIV) H1N1 pandemic has caused more than 18,000 deaths worldwide. Vaccines against the 2009 A/H1N1 influenza virus are useful for preventing infection and controlling the pandemic. The kinetics of the immune response following vaccination with the 2009 A/H1N1 influenza vaccine need further investigation. METHODOLOGY/PRINCIPAL FINDINGS: 58 volunteers were vaccinated with a 2009 A/H1N1 pandemic influenza monovalent split-virus vaccine (15 µg, single-dose). The sera were collected before Day 0 (pre-vaccination) and on Days 3, 5, 10, 14, 21, 30, 45 and 60 post vaccination. Specific antibody responses induced by the vaccination were analyzed using hemagglutination inhibition (HI) assay and enzyme-linked immunosorbent assay (ELISA). After administration of the 2009 A/H1N1 influenza vaccine, specific and protective antibody response with a major subtype of IgG was sufficiently developed as early as Day 10 (seroprotection rate: 93%). This specific antibody response could maintain for at least 60 days without significant reduction. Antibody response induced by the 2009 A/H1N1 influenza vaccine could not render protection against seasonal H1N1 influenza (seroconversion rate: 3% on Day 21). However, volunteers with higher pre-existing seasonal influenza antibody levels (pre-vaccination HI titer ≥1∶40, Group 1) more easily developed a strong antibody protection effect against the 2009 A/H1N1 influenza vaccine as compared with those showing lower pre-existing seasonal influenza antibody levels (pre-vaccination HI titer <1∶40, Group 2). The titer of the specific antibody against the 2009 A/H1N1 influenza was much higher in Group 1 (geometric mean titer: 146 on Day 21) than that in Group 2 (geometric mean titer: 70 on Day 21). CONCLUSIONS/SIGNIFICANCE: Recipients could gain sufficient protection as early as 10 days after vaccine administration. The protection could last at least 60 days. Individuals with a stronger pre-existing seasonal influenza antibody response may have a relatively higher potential for developing a stronger humoral immune response after vaccination with the 2009 A/H1N1 pandemic influenza vaccine.
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spelling pubmed-30003352010-12-13 Immune Protection Induced on Day 10 Following Administration of the 2009 A/H1N1 Pandemic Influenza Vaccine Sun, Yizhuo Bian, Chao Xu, Ke Hu, Weibin Wang, Tongyan Cui, Jun Wu, Hongqiang Ling, Zhiyang Ji, Yongyong Lin, Guomei Tian, Lin Zhou, Yanyan Li, Bingnan Hu, Guiyu Yu, Ning An, Wenqi Pan, Ruowen Zhou, Paul Leng, Qibin Huang, Zhong Ma, Xiaowei Sun, Bing PLoS One Research Article BACKGROUND: The 2009 swine-origin influenza virus (S-OIV) H1N1 pandemic has caused more than 18,000 deaths worldwide. Vaccines against the 2009 A/H1N1 influenza virus are useful for preventing infection and controlling the pandemic. The kinetics of the immune response following vaccination with the 2009 A/H1N1 influenza vaccine need further investigation. METHODOLOGY/PRINCIPAL FINDINGS: 58 volunteers were vaccinated with a 2009 A/H1N1 pandemic influenza monovalent split-virus vaccine (15 µg, single-dose). The sera were collected before Day 0 (pre-vaccination) and on Days 3, 5, 10, 14, 21, 30, 45 and 60 post vaccination. Specific antibody responses induced by the vaccination were analyzed using hemagglutination inhibition (HI) assay and enzyme-linked immunosorbent assay (ELISA). After administration of the 2009 A/H1N1 influenza vaccine, specific and protective antibody response with a major subtype of IgG was sufficiently developed as early as Day 10 (seroprotection rate: 93%). This specific antibody response could maintain for at least 60 days without significant reduction. Antibody response induced by the 2009 A/H1N1 influenza vaccine could not render protection against seasonal H1N1 influenza (seroconversion rate: 3% on Day 21). However, volunteers with higher pre-existing seasonal influenza antibody levels (pre-vaccination HI titer ≥1∶40, Group 1) more easily developed a strong antibody protection effect against the 2009 A/H1N1 influenza vaccine as compared with those showing lower pre-existing seasonal influenza antibody levels (pre-vaccination HI titer <1∶40, Group 2). The titer of the specific antibody against the 2009 A/H1N1 influenza was much higher in Group 1 (geometric mean titer: 146 on Day 21) than that in Group 2 (geometric mean titer: 70 on Day 21). CONCLUSIONS/SIGNIFICANCE: Recipients could gain sufficient protection as early as 10 days after vaccine administration. The protection could last at least 60 days. Individuals with a stronger pre-existing seasonal influenza antibody response may have a relatively higher potential for developing a stronger humoral immune response after vaccination with the 2009 A/H1N1 pandemic influenza vaccine. Public Library of Science 2010-12-09 /pmc/articles/PMC3000335/ /pubmed/21151563 http://dx.doi.org/10.1371/journal.pone.0014270 Text en Sun et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Sun, Yizhuo
Bian, Chao
Xu, Ke
Hu, Weibin
Wang, Tongyan
Cui, Jun
Wu, Hongqiang
Ling, Zhiyang
Ji, Yongyong
Lin, Guomei
Tian, Lin
Zhou, Yanyan
Li, Bingnan
Hu, Guiyu
Yu, Ning
An, Wenqi
Pan, Ruowen
Zhou, Paul
Leng, Qibin
Huang, Zhong
Ma, Xiaowei
Sun, Bing
Immune Protection Induced on Day 10 Following Administration of the 2009 A/H1N1 Pandemic Influenza Vaccine
title Immune Protection Induced on Day 10 Following Administration of the 2009 A/H1N1 Pandemic Influenza Vaccine
title_full Immune Protection Induced on Day 10 Following Administration of the 2009 A/H1N1 Pandemic Influenza Vaccine
title_fullStr Immune Protection Induced on Day 10 Following Administration of the 2009 A/H1N1 Pandemic Influenza Vaccine
title_full_unstemmed Immune Protection Induced on Day 10 Following Administration of the 2009 A/H1N1 Pandemic Influenza Vaccine
title_short Immune Protection Induced on Day 10 Following Administration of the 2009 A/H1N1 Pandemic Influenza Vaccine
title_sort immune protection induced on day 10 following administration of the 2009 a/h1n1 pandemic influenza vaccine
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3000335/
https://www.ncbi.nlm.nih.gov/pubmed/21151563
http://dx.doi.org/10.1371/journal.pone.0014270
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