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The dynamics of infection and the persistence of immunity to A(H1N1)pdm09 virus in Israel

BACKGROUND: Influenza virus A(H1N1)pdm09 first appeared in Israel in late April 2009, disappeared in mid‐March 2010, and reappeared in late October 2010. Symptoms were mostly mild without need for medical care. OBJECTIVES: To provide targets for future pandemic preparedness and response by evaluatin...

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Autores principales: Weil, Merav, Shohat, Tamar, Bromberg, Michal, Bassal, Ravit, Dichtiar, Rita, Mandelboim, Michal, Sofer, Danit, Cohen, Dani, Mendelson, Ella
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5781219/
https://www.ncbi.nlm.nih.gov/pubmed/23280061
http://dx.doi.org/10.1111/irv.12071
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author Weil, Merav
Shohat, Tamar
Bromberg, Michal
Bassal, Ravit
Dichtiar, Rita
Mandelboim, Michal
Sofer, Danit
Cohen, Dani
Mendelson, Ella
author_facet Weil, Merav
Shohat, Tamar
Bromberg, Michal
Bassal, Ravit
Dichtiar, Rita
Mandelboim, Michal
Sofer, Danit
Cohen, Dani
Mendelson, Ella
author_sort Weil, Merav
collection PubMed
description BACKGROUND: Influenza virus A(H1N1)pdm09 first appeared in Israel in late April 2009, disappeared in mid‐March 2010, and reappeared in late October 2010. Symptoms were mostly mild without need for medical care. OBJECTIVES: To provide targets for future pandemic preparedness and response by evaluating the dynamics and cumulative incidence of A(H1N1)pdm09 infection, the virus‐specific seroprevalence (HI antibody titer >1:40) at the height of the pandemic, during its decline and thereafter. METHODS: A cross‐sectional seroepidemiological study was conducted on 6911 serum samples collected before, during, and after the pandemic. RESULTS: Cumulative incidence of infection derived from the differences between post‐ and pre‐pandemic seroprevalence was 54·1%, 32·9%, 22·9%, 14·8%, and 6·3% in age‐groups 0–9, 10–19, 20–49, 50–79, and ≥80 years, respectively, and 28·5% for all age‐groups combined. Vaccination could have contributed at the most 4·6% to the post‐pandemic population seroprevalence. High pre‐pandemic immune response (47·4%) found in a cohort aged 15–18 year was strongly associated with birth years 1990–1993. Morbidity began to decline in mid‐November 2009 at 32·8% population seroprevalence (45% in ages 0–19 year) and stopped in March 2010 at 43·4% population seroprevalence in February 2010 (70% in ages 0–19 year). Between February and September 2010, seroprevalence declined by 12·2% allowing virus recirculation from October 2010. CONCLUSIONS: Our study provides targets for controlling future influenza pandemics in Israel. Vaccination should focus on the younger age‐groups (0–19 year) which played a key role in transmission of the A(H1N1)pdm09 due to lack of background immunity (ages 0–9 year) and high exposure rates (ages 10–19 year).
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spelling pubmed-57812192018-02-06 The dynamics of infection and the persistence of immunity to A(H1N1)pdm09 virus in Israel Weil, Merav Shohat, Tamar Bromberg, Michal Bassal, Ravit Dichtiar, Rita Mandelboim, Michal Sofer, Danit Cohen, Dani Mendelson, Ella Influenza Other Respir Viruses Part 2 Pandemic H1N1 Papers BACKGROUND: Influenza virus A(H1N1)pdm09 first appeared in Israel in late April 2009, disappeared in mid‐March 2010, and reappeared in late October 2010. Symptoms were mostly mild without need for medical care. OBJECTIVES: To provide targets for future pandemic preparedness and response by evaluating the dynamics and cumulative incidence of A(H1N1)pdm09 infection, the virus‐specific seroprevalence (HI antibody titer >1:40) at the height of the pandemic, during its decline and thereafter. METHODS: A cross‐sectional seroepidemiological study was conducted on 6911 serum samples collected before, during, and after the pandemic. RESULTS: Cumulative incidence of infection derived from the differences between post‐ and pre‐pandemic seroprevalence was 54·1%, 32·9%, 22·9%, 14·8%, and 6·3% in age‐groups 0–9, 10–19, 20–49, 50–79, and ≥80 years, respectively, and 28·5% for all age‐groups combined. Vaccination could have contributed at the most 4·6% to the post‐pandemic population seroprevalence. High pre‐pandemic immune response (47·4%) found in a cohort aged 15–18 year was strongly associated with birth years 1990–1993. Morbidity began to decline in mid‐November 2009 at 32·8% population seroprevalence (45% in ages 0–19 year) and stopped in March 2010 at 43·4% population seroprevalence in February 2010 (70% in ages 0–19 year). Between February and September 2010, seroprevalence declined by 12·2% allowing virus recirculation from October 2010. CONCLUSIONS: Our study provides targets for controlling future influenza pandemics in Israel. Vaccination should focus on the younger age‐groups (0–19 year) which played a key role in transmission of the A(H1N1)pdm09 due to lack of background immunity (ages 0–9 year) and high exposure rates (ages 10–19 year). John Wiley and Sons Inc. 2012-12-22 2013-09 /pmc/articles/PMC5781219/ /pubmed/23280061 http://dx.doi.org/10.1111/irv.12071 Text en © 2012 John Wiley & Sons Ltd
spellingShingle Part 2 Pandemic H1N1 Papers
Weil, Merav
Shohat, Tamar
Bromberg, Michal
Bassal, Ravit
Dichtiar, Rita
Mandelboim, Michal
Sofer, Danit
Cohen, Dani
Mendelson, Ella
The dynamics of infection and the persistence of immunity to A(H1N1)pdm09 virus in Israel
title The dynamics of infection and the persistence of immunity to A(H1N1)pdm09 virus in Israel
title_full The dynamics of infection and the persistence of immunity to A(H1N1)pdm09 virus in Israel
title_fullStr The dynamics of infection and the persistence of immunity to A(H1N1)pdm09 virus in Israel
title_full_unstemmed The dynamics of infection and the persistence of immunity to A(H1N1)pdm09 virus in Israel
title_short The dynamics of infection and the persistence of immunity to A(H1N1)pdm09 virus in Israel
title_sort dynamics of infection and the persistence of immunity to a(h1n1)pdm09 virus in israel
topic Part 2 Pandemic H1N1 Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5781219/
https://www.ncbi.nlm.nih.gov/pubmed/23280061
http://dx.doi.org/10.1111/irv.12071
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