Age-related heterologous antibody responses to influenza virus vaccination.
Identifieur interne : 002C04 ( Main/Merge ); précédent : 002C03; suivant : 002C05Age-related heterologous antibody responses to influenza virus vaccination.
Auteurs : G R Noble ; H S Kaye ; A P Kendal ; W R DowdleSource :
- The Journal of infectious diseases [ 0022-1899 ] ; 1977.
Descripteurs français
- KwdFr :
- MESH :
- biosynthèse : Anticorps antiviraux.
- immunologie : Virus de la grippe A.
- pharmacologie : Vaccins antigrippaux.
- Adolescent, Adulte, Adulte d'âge moyen, Angleterre, Facteurs temps, Humains, New Jersey, Vaccination, Vieillissement.
English descriptors
- KwdEn :
- MESH :
- chemical , biosynthesis : Antibodies, Viral.
- chemical , pharmacology : Influenza Vaccines.
- geographic : England, New Jersey.
- immunology : Influenza A virus.
- Adolescent, Adult, Aging, Humans, Middle Aged, Time Factors, Vaccination.
Abstract
Heterologous hemagglutination-inhibiting (HAI) antibody responses to influenza A/New Jersey/76 (Hsw1N1) virus vaccine were examined in individuals receiving doses of 200, 400, or 800 chick cell-agglutinating units of whole-virus or split-virus products during the 1976 National Influenza Vaccine Test Program. Vaccination with influenza A/New Jersey/76 virus produced a high rate of heterologous antibody response to influenza A/PR/8/34 (H0N1) and A/FM/1/47 (H1N1) viruses in persons whose original antigenic experience according to their age was with H0N1 or H1N1 strains, respectively. Vaccination with A/New Jersey/76 virus produced only low levels of HAI antibody to influenza A/Japan/305/57 (H2N2) and A/Victoria/3/75 (H3N2) viruses, and these responses were less clearly related to primary infections. Thus the greatest heterologous HAI antibody responses occurred when there were shared antigenic determinants between the hemagglutinins of the vaccine virus and the viruses that had caused the initial priming infection. However, when vaccinations or infections with H3N2 and Hsw1N1 strains may both be occurring in the population, even infrequent formation of heterologous antibody may make it difficult to interpret serologic data precisely.
DOI: 10.1093/infdis/136.supplement_3.s686
PubMed: 606792
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pubmed:606792Le document en format XML
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<term>Adult</term>
<term>Aging</term>
<term>Antibodies, Viral (biosynthesis)</term>
<term>England</term>
<term>Humans</term>
<term>Influenza A virus (immunology)</term>
<term>Influenza Vaccines (pharmacology)</term>
<term>Middle Aged</term>
<term>New Jersey</term>
<term>Time Factors</term>
<term>Vaccination</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr"><term>Adolescent</term>
<term>Adulte</term>
<term>Adulte d'âge moyen</term>
<term>Angleterre</term>
<term>Anticorps antiviraux (biosynthèse)</term>
<term>Facteurs temps</term>
<term>Humains</term>
<term>New Jersey</term>
<term>Vaccination</term>
<term>Vaccins antigrippaux (pharmacologie)</term>
<term>Vieillissement</term>
<term>Virus de la grippe A (immunologie)</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="biosynthesis" xml:lang="en"><term>Antibodies, Viral</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="pharmacology" xml:lang="en"><term>Influenza Vaccines</term>
</keywords>
<keywords scheme="MESH" type="geographic" xml:lang="en"><term>England</term>
<term>New Jersey</term>
</keywords>
<keywords scheme="MESH" qualifier="biosynthèse" xml:lang="fr"><term>Anticorps antiviraux</term>
</keywords>
<keywords scheme="MESH" qualifier="immunologie" xml:lang="fr"><term>Virus de la grippe A</term>
</keywords>
<keywords scheme="MESH" qualifier="immunology" xml:lang="en"><term>Influenza A virus</term>
</keywords>
<keywords scheme="MESH" qualifier="pharmacologie" xml:lang="fr"><term>Vaccins antigrippaux</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Adolescent</term>
<term>Adult</term>
<term>Aging</term>
<term>Humans</term>
<term>Middle Aged</term>
<term>Time Factors</term>
<term>Vaccination</term>
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<keywords scheme="MESH" xml:lang="fr"><term>Adolescent</term>
<term>Adulte</term>
<term>Adulte d'âge moyen</term>
<term>Angleterre</term>
<term>Facteurs temps</term>
<term>Humains</term>
<term>New Jersey</term>
<term>Vaccination</term>
<term>Vieillissement</term>
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<front><div type="abstract" xml:lang="en">Heterologous hemagglutination-inhibiting (HAI) antibody responses to influenza A/New Jersey/76 (Hsw1N1) virus vaccine were examined in individuals receiving doses of 200, 400, or 800 chick cell-agglutinating units of whole-virus or split-virus products during the 1976 National Influenza Vaccine Test Program. Vaccination with influenza A/New Jersey/76 virus produced a high rate of heterologous antibody response to influenza A/PR/8/34 (H0N1) and A/FM/1/47 (H1N1) viruses in persons whose original antigenic experience according to their age was with H0N1 or H1N1 strains, respectively. Vaccination with A/New Jersey/76 virus produced only low levels of HAI antibody to influenza A/Japan/305/57 (H2N2) and A/Victoria/3/75 (H3N2) viruses, and these responses were less clearly related to primary infections. Thus the greatest heterologous HAI antibody responses occurred when there were shared antigenic determinants between the hemagglutinins of the vaccine virus and the viruses that had caused the initial priming infection. However, when vaccinations or infections with H3N2 and Hsw1N1 strains may both be occurring in the population, even infrequent formation of heterologous antibody may make it difficult to interpret serologic data precisely.</div>
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