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Immuno-epidemiologic Correlates of Pandemic H1N1 Surveillance Observations: Higher Antibody and Lower Cell-Mediated Immune Responses with Advanced Age

Identifieur interne : 000059 ( PascalFrancis/Curation ); précédent : 000058; suivant : 000060

Immuno-epidemiologic Correlates of Pandemic H1N1 Surveillance Observations: Higher Antibody and Lower Cell-Mediated Immune Responses with Advanced Age

Auteurs : Danuta M. Skowronski [Canada] ; Travis S. Hottes [Canada] ; Janet E. Mcelhaney [Canada] ; Naveed Z. Janjua [Canada] ; Suzana Sabaiduc [Canada] ; Tracy Chan [Canada] ; Beth Gentleman [Canada] ; Dale Purych [Canada] ; Jennifer Gardy [Canada] ; David M. Patrick [Canada] ; Robert C. Brunham [Canada] ; Gaston De Serres [Canada] ; Martin Petric [Canada]

Source :

RBID : Pascal:11-0131918

Descripteurs français

English descriptors

Abstract

Background. Pandemic H1N1 (pH1N1) surveillance data showed lower attack rates but higher risk of severe outcomes with advanced age. We explored immuno-epidemiologic correlates of surveillance findings including humoral and cell-mediated immunity (CMI). Methods. In an age-based design, ∼100 banked/residual sera per 10-year age stratum were assessed by hemagglutination inhibition (HI) and microneutralization (MN) assays for preexisting antibody to pH1N1 and recent seasonal H1N1 and H3N2 strains. In a separate birth cohort design defined by childhood influenza A/subtype priming (1919-1929: H1N1; 1945-1949: H1N1; 1958-1960: H2N2; 1969-1970: H3N2; 1978-1989: H3N2/H1N1), whole blood was collected from up to 50 volunteers per birth cohort. The ratio of Th1(IFN-γ):Th2(IL-10) cytokine responses was evaluated in vitro. Results. Antibody to seasonal viruses was highest in school-age children. Cross-reactive HI/MN antibody to pH1N1 was low among participants <70 years of age (yoa; 6%/4% ≥ 40), but seroprevalence increased at 70-79 yoa (27%/6%), increased even more at 80-89 yoa (65%/47%), and was highest at ≥90 yoa (88%/76%). CMI to pH1N1 was evident in all 5 birth cohorts but was lower compared with seasonal strains. There was little differentiation by subtype priming, but the Th1:Th2 ratio for all viruses dropped significantly in the 2 oldest cohorts. Conclusions. Preexisting antibody may have protected the very old from pH1N1 infection, while diminished CMI may have contributed to greater severity once infected. In the young, cross-reactive pH1N1 antibody was mostly absent, while more intact CMI may have protected against severe outcomes.
pA  
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A11 01  1    @1 SKOWRONSKI (Danuta M.)
A11 02  1    @1 HOTTES (Travis S.)
A11 03  1    @1 MCELHANEY (Janet E.)
A11 04  1    @1 JANJUA (Naveed Z.)
A11 05  1    @1 SABAIDUC (Suzana)
A11 06  1    @1 CHAN (Tracy)
A11 07  1    @1 GENTLEMAN (Beth)
A11 08  1    @1 PURYCH (Dale)
A11 09  1    @1 GARDY (Jennifer)
A11 10  1    @1 PATRICK (David M.)
A11 11  1    @1 BRUNHAM (Robert C.)
A11 12  1    @1 DE SERRES (Gaston)
A11 13  1    @1 PETRIC (Martin)
A14 01      @1 British Columbia Centre for Disease Control, University of British Columbia @3 CAN @Z 1 aut. @Z 2 aut. @Z 4 aut. @Z 5 aut. @Z 6 aut. @Z 9 aut. @Z 10 aut. @Z 11 aut. @Z 13 aut.
A14 02      @1 School of Population and Public Health, University of British Columbia @3 CAN @Z 1 aut. @Z 4 aut. @Z 10 aut.
A14 03      @1 Department of Medicine, University of British Columbia @3 CAN @Z 3 aut. @Z 7 aut. @Z 11 aut.
A14 04      @1 Department of Microbiology and Immunology, University of British Columbia @3 CAN @Z 9 aut.
A14 05      @1 Department of Pathology and Laboratory Medicine, University of British Columbia @3 CAN @Z 13 aut.
A14 06      @1 Vancouver Coastal Health Research Institute @2 Vancouver @3 CAN @Z 3 aut. @Z 7 aut.
A14 07      @1 BC Biomedical Laboratories Ltd @2 Surrey, British Columbia @3 CAN @Z 8 aut.
A14 08      @1 Institut national de santé publique du Québec, Université Laval @2 Québec @3 CAN @Z 12 aut.
A14 09      @1 Department of Social and Preventive Medicine, Université Laval @2 Québec @3 CAN @Z 12 aut.
A20       @1 158-167
A21       @1 2011
A23 01      @0 ENG
A43 01      @1 INIST @2 2052 @5 354000194614000050
A44       @0 0000 @1 © 2011 INIST-CNRS. All rights reserved.
A45       @0 41 ref.
A47 01  1    @0 11-0131918
A60       @1 P
A61       @0 A
A64 01  1    @0 The Journal of infectious diseases
A66 01      @0 GBR
C01 01    ENG  @0 Background. Pandemic H1N1 (pH1N1) surveillance data showed lower attack rates but higher risk of severe outcomes with advanced age. We explored immuno-epidemiologic correlates of surveillance findings including humoral and cell-mediated immunity (CMI). Methods. In an age-based design, ∼100 banked/residual sera per 10-year age stratum were assessed by hemagglutination inhibition (HI) and microneutralization (MN) assays for preexisting antibody to pH1N1 and recent seasonal H1N1 and H3N2 strains. In a separate birth cohort design defined by childhood influenza A/subtype priming (1919-1929: H1N1; 1945-1949: H1N1; 1958-1960: H2N2; 1969-1970: H3N2; 1978-1989: H3N2/H1N1), whole blood was collected from up to 50 volunteers per birth cohort. The ratio of Th1(IFN-γ):Th2(IL-10) cytokine responses was evaluated in vitro. Results. Antibody to seasonal viruses was highest in school-age children. Cross-reactive HI/MN antibody to pH1N1 was low among participants <70 years of age (yoa; 6%/4% ≥ 40), but seroprevalence increased at 70-79 yoa (27%/6%), increased even more at 80-89 yoa (65%/47%), and was highest at ≥90 yoa (88%/76%). CMI to pH1N1 was evident in all 5 birth cohorts but was lower compared with seasonal strains. There was little differentiation by subtype priming, but the Th1:Th2 ratio for all viruses dropped significantly in the 2 oldest cohorts. Conclusions. Preexisting antibody may have protected the very old from pH1N1 infection, while diminished CMI may have contributed to greater severity once infected. In the young, cross-reactive pH1N1 antibody was mostly absent, while more intact CMI may have protected against severe outcomes.
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C03 03  X  FRE  @0 Age @5 07
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C03 03  X  SPA  @0 Edad @5 07
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C03 04  X  ENG  @0 Infection @5 08
C03 04  X  SPA  @0 Infección @5 08
C03 05  X  FRE  @0 Virus grippal A(H1N1) @4 CD @5 96
C03 05  X  ENG  @0 Influenzavirus A(H1N1) @4 CD @5 96
N21       @1 087
N44 01      @1 OTO
N82       @1 OTO

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Pascal:11-0131918

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<name sortKey="Petric, Martin" sort="Petric, Martin" uniqKey="Petric M" first="Martin" last="Petric">Martin Petric</name>
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<series>
<title level="j" type="main">The Journal of infectious diseases</title>
<title level="j" type="abbreviated">J. infect. dis.</title>
<idno type="ISSN">0022-1899</idno>
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<date when="2011">2011</date>
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<title level="j" type="main">The Journal of infectious diseases</title>
<title level="j" type="abbreviated">J. infect. dis.</title>
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<term>Age</term>
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<div type="abstract" xml:lang="en">Background. Pandemic H1N1 (pH1N1) surveillance data showed lower attack rates but higher risk of severe outcomes with advanced age. We explored immuno-epidemiologic correlates of surveillance findings including humoral and cell-mediated immunity (CMI). Methods. In an age-based design, ∼100 banked/residual sera per 10-year age stratum were assessed by hemagglutination inhibition (HI) and microneutralization (MN) assays for preexisting antibody to pH1N1 and recent seasonal H1N1 and H3N2 strains. In a separate birth cohort design defined by childhood influenza A/subtype priming (1919-1929: H1N1; 1945-1949: H1N1; 1958-1960: H2N2; 1969-1970: H3N2; 1978-1989: H3N2/H1N1), whole blood was collected from up to 50 volunteers per birth cohort. The ratio of Th1(IFN-γ):Th2(IL-10) cytokine responses was evaluated in vitro. Results. Antibody to seasonal viruses was highest in school-age children. Cross-reactive HI/MN antibody to pH1N1 was low among participants <70 years of age (yoa; 6%/4% ≥ 40), but seroprevalence increased at 70-79 yoa (27%/6%), increased even more at 80-89 yoa (65%/47%), and was highest at ≥90 yoa (88%/76%). CMI to pH1N1 was evident in all 5 birth cohorts but was lower compared with seasonal strains. There was little differentiation by subtype priming, but the Th1:Th2 ratio for all viruses dropped significantly in the 2 oldest cohorts. Conclusions. Preexisting antibody may have protected the very old from pH1N1 infection, while diminished CMI may have contributed to greater severity once infected. In the young, cross-reactive pH1N1 antibody was mostly absent, while more intact CMI may have protected against severe outcomes.</div>
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