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Immunogenicity of influenza A(H1N1)pdm09 vaccine and the associated factors on lowered immune response in patients with hepatitis C

Background  Patients with underlying disease represent a high‐risk group for influenza‐associated complications and hospitalization. However, few studies investigated the immunogenicity of influenza vaccine in patients with liver disease. Objective  To examine immunogenicity of influenza A(H1N1)pdm0...

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Autores principales: Ohfuji, Satoko, Fukushima, Wakaba, Tamori, Akihiro, Maeda, Kazuhiro, Maeda, Akiko, Hirota, Yoshio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5779820/
https://www.ncbi.nlm.nih.gov/pubmed/22897938
http://dx.doi.org/10.1111/j.1750-2659.2012.00424.x
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author Ohfuji, Satoko
Fukushima, Wakaba
Tamori, Akihiro
Maeda, Kazuhiro
Maeda, Akiko
Hirota, Yoshio
author_facet Ohfuji, Satoko
Fukushima, Wakaba
Tamori, Akihiro
Maeda, Kazuhiro
Maeda, Akiko
Hirota, Yoshio
author_sort Ohfuji, Satoko
collection PubMed
description Background  Patients with underlying disease represent a high‐risk group for influenza‐associated complications and hospitalization. However, few studies investigated the immunogenicity of influenza vaccine in patients with liver disease. Objective  To examine immunogenicity of influenza A(H1N1)pdm09 vaccine in patients with liver disease and to explore the associated factors on lowered immune response. Patients/Methods  A single subcutaneous dose of monovalent inactivated unadjuvanted split‐virus influenza A(H1N1)pdm09 vaccination was performed in 80 patients with chronic hepatitis C virus infection at Osaka City University Hospital in Japan. To measure the hemagglutination inhibition antibody titer, serum samples were collected before and 3 weeks after vaccination. Results  No serious adverse events were observed. After vaccination, antibody titers ≥1:40 were observed in 56 patients (71%). The corresponding seroconversion proportion was 72%, and the mean fold rise was 10·3. Immune responses were robust regardless of severity of liver disease or existence of probable cirrhosis. However, patients with older age, lower body mass index, or receiving Stronger Neo‐Minophagen C tended to show lower antibody responses to A(H1N1)pdm09 vaccine. In addition, reduced immune responses were observed in patients who had received the 2009/10 seasonal vaccination prior to A(H1N1)pdm09 vaccination. Conclusions  Single dose of A(H1N1)pdm09 vaccine achieved a sufficient level of immunity among patients with chronic hepatitis C. Antibody response may be affected by age, body mass index, Stronger Neo‐Minophagen C administration, and recent seasonal influenza vaccination.
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spelling pubmed-57798202018-02-05 Immunogenicity of influenza A(H1N1)pdm09 vaccine and the associated factors on lowered immune response in patients with hepatitis C Ohfuji, Satoko Fukushima, Wakaba Tamori, Akihiro Maeda, Kazuhiro Maeda, Akiko Hirota, Yoshio Influenza Other Respir Viruses Part 2 A(H1N1)pdm09 Papers Background  Patients with underlying disease represent a high‐risk group for influenza‐associated complications and hospitalization. However, few studies investigated the immunogenicity of influenza vaccine in patients with liver disease. Objective  To examine immunogenicity of influenza A(H1N1)pdm09 vaccine in patients with liver disease and to explore the associated factors on lowered immune response. Patients/Methods  A single subcutaneous dose of monovalent inactivated unadjuvanted split‐virus influenza A(H1N1)pdm09 vaccination was performed in 80 patients with chronic hepatitis C virus infection at Osaka City University Hospital in Japan. To measure the hemagglutination inhibition antibody titer, serum samples were collected before and 3 weeks after vaccination. Results  No serious adverse events were observed. After vaccination, antibody titers ≥1:40 were observed in 56 patients (71%). The corresponding seroconversion proportion was 72%, and the mean fold rise was 10·3. Immune responses were robust regardless of severity of liver disease or existence of probable cirrhosis. However, patients with older age, lower body mass index, or receiving Stronger Neo‐Minophagen C tended to show lower antibody responses to A(H1N1)pdm09 vaccine. In addition, reduced immune responses were observed in patients who had received the 2009/10 seasonal vaccination prior to A(H1N1)pdm09 vaccination. Conclusions  Single dose of A(H1N1)pdm09 vaccine achieved a sufficient level of immunity among patients with chronic hepatitis C. Antibody response may be affected by age, body mass index, Stronger Neo‐Minophagen C administration, and recent seasonal influenza vaccination. Blackwell Publishing Ltd 2012-08-16 2013-05 /pmc/articles/PMC5779820/ /pubmed/22897938 http://dx.doi.org/10.1111/j.1750-2659.2012.00424.x Text en © 2012 Blackwell Publishing Ltd
spellingShingle Part 2 A(H1N1)pdm09 Papers
Ohfuji, Satoko
Fukushima, Wakaba
Tamori, Akihiro
Maeda, Kazuhiro
Maeda, Akiko
Hirota, Yoshio
Immunogenicity of influenza A(H1N1)pdm09 vaccine and the associated factors on lowered immune response in patients with hepatitis C
title Immunogenicity of influenza A(H1N1)pdm09 vaccine and the associated factors on lowered immune response in patients with hepatitis C
title_full Immunogenicity of influenza A(H1N1)pdm09 vaccine and the associated factors on lowered immune response in patients with hepatitis C
title_fullStr Immunogenicity of influenza A(H1N1)pdm09 vaccine and the associated factors on lowered immune response in patients with hepatitis C
title_full_unstemmed Immunogenicity of influenza A(H1N1)pdm09 vaccine and the associated factors on lowered immune response in patients with hepatitis C
title_short Immunogenicity of influenza A(H1N1)pdm09 vaccine and the associated factors on lowered immune response in patients with hepatitis C
title_sort immunogenicity of influenza a(h1n1)pdm09 vaccine and the associated factors on lowered immune response in patients with hepatitis c
topic Part 2 A(H1N1)pdm09 Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5779820/
https://www.ncbi.nlm.nih.gov/pubmed/22897938
http://dx.doi.org/10.1111/j.1750-2659.2012.00424.x
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