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The A/Mallard/67S0/78 Avian-Human, but Not the A/Ann Arbor/6/60 Cold-Adapted, Influenza A/Kawasaki/86 (H1N1) Reassortant Virus Vaccine Retains Partial Virulence for Infants and Children

Identifieur interne : 000948 ( Istex/Corpus ); précédent : 000947; suivant : 000949

The A/Mallard/67S0/78 Avian-Human, but Not the A/Ann Arbor/6/60 Cold-Adapted, Influenza A/Kawasaki/86 (H1N1) Reassortant Virus Vaccine Retains Partial Virulence for Infants and Children

Auteurs : Mark C. Steinhoff ; Neal A. Halsey ; Louis F. Fries ; Modena H. Wilson ; James King ; Barbara A. Burns ; Roberta K. Samorodin ; Victoria Perkis ; Brian R. Murphy ; Mary Lou Clements

Source :

RBID : ISTEX:D6F40AA0B98E981622A2A7C9177CE75592A0B434

Abstract

Characteristics of avian-human (ab) and cold-adapted (ca) influenza A/Kawasaki/9/86 (H1N1) reassortant vaccine viruses were compared in 37 seronegative adults and 122 seronegative infants and children. The 50% human infectious dose (HID50) in infants and children was 102.9 and 102.6 TCID50 for the ab and ca vaccine, respectively. The ah influenza A/Kawasaki/9/86 reassortant was reactogenic: 24% of infants and children infected with ⩾100 HID50 had fever ⩾39.4°C. Since H3N2 ah vaccines were previously shown to be adequately attenuated, it is reasonable to suggest that the genes that code for hemagglutinin and neuraminidase of the H1N1 virus apparently influence the reactogenicity of reassort antviruses derived from the avian influenza A/Mallard/NewYork/6750/78 donor virus. Because this avian virus does not reproducibly confer a satisfactory level of attenuation to each subtype of influenza A virus, it is not a suitable donor virus for attenuation of wild-typeinfluenza viruses. In contrast, the ca A/AnnArbor/6/60 donor virus reliably confers attenuation characteristics to a variety of H1N1 and H3N2 influenza A viruses.

Url:
DOI: 10.1093/infdis/163.5.1023

Links to Exploration step

ISTEX:D6F40AA0B98E981622A2A7C9177CE75592A0B434

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<p>Characteristics of avian-human (ab) and cold-adapted (ca) influenza A/Kawasaki/9/86 (H1N1) reassortant vaccine viruses were compared in 37 seronegative adults and 122 seronegative infants and children. The 50% human infectious dose (HID
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<p>Characteristics of avian-human (ab) and cold-adapted (ca) influenza A/Kawasaki/9/86 (H1N1) reassortant vaccine viruses were compared in 37 seronegative adults and 122 seronegative infants and children. The 50% human infectious dose (HID
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<namePart type="given">Neal A.</namePart>
<namePart type="family">Halsey</namePart>
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<namePart type="given">Louis F.</namePart>
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<namePart type="given">Modena H.</namePart>
<namePart type="family">Wilson</namePart>
<affiliation>Center for Immunization Research, Department of International Health, Johns Hopkins University School of Hygiene and Public Health, and Departments of Pediatrics and Medicine, Johns Hopkins University School of Medicine, Baltimore, Bethesda, Maryland</affiliation>
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<namePart type="given">James</namePart>
<namePart type="family">King</namePart>
<affiliation>Center for Immunization Research, Department of International Health, Johns Hopkins University School of Hygiene and Public Health, and Departments of Pediatrics and Medicine, Johns Hopkins University School of Medicine, Baltimore, Bethesda, Maryland</affiliation>
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<namePart type="given">Barbara A.</namePart>
<namePart type="family">Burns</namePart>
<affiliation>Center for Immunization Research, Department of International Health, Johns Hopkins University School of Hygiene and Public Health, and Departments of Pediatrics and Medicine, Johns Hopkins University School of Medicine, Baltimore, Bethesda, Maryland</affiliation>
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<namePart type="given">Roberta K.</namePart>
<namePart type="family">Samorodin</namePart>
<affiliation>Center for Immunization Research, Department of International Health, Johns Hopkins University School of Hygiene and Public Health, and Departments of Pediatrics and Medicine, Johns Hopkins University School of Medicine, Baltimore, Bethesda, Maryland</affiliation>
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<namePart type="given">Brian R.</namePart>
<namePart type="family">Murphy</namePart>
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<name type="personal">
<namePart type="given">Mary Lou</namePart>
<namePart type="family">Clements</namePart>
<affiliation>Center for Immunization Research, Department of International Health, Johns Hopkins University School of Hygiene and Public Health, and Departments of Pediatrics and Medicine, Johns Hopkins University School of Medicine, Baltimore, Bethesda, Maryland</affiliation>
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<abstract>Characteristics of avian-human (ab) and cold-adapted (ca) influenza A/Kawasaki/9/86 (H1N1) reassortant vaccine viruses were compared in 37 seronegative adults and 122 seronegative infants and children. The 50% human infectious dose (HID50) in infants and children was 102.9 and 102.6 TCID50 for the ab and ca vaccine, respectively. The ah influenza A/Kawasaki/9/86 reassortant was reactogenic: 24% of infants and children infected with ⩾100 HID50 had fever ⩾39.4°C. Since H3N2 ah vaccines were previously shown to be adequately attenuated, it is reasonable to suggest that the genes that code for hemagglutinin and neuraminidase of the H1N1 virus apparently influence the reactogenicity of reassort antviruses derived from the avian influenza A/Mallard/NewYork/6750/78 donor virus. Because this avian virus does not reproducibly confer a satisfactory level of attenuation to each subtype of influenza A virus, it is not a suitable donor virus for attenuation of wild-typeinfluenza viruses. In contrast, the ca A/AnnArbor/6/60 donor virus reliably confers attenuation characteristics to a variety of H1N1 and H3N2 influenza A viruses.</abstract>
<note type="author-notes">Reprints or correspondence: Dr. Mark C. Steinhoff, Johns Hopkins University, Center for Immunization Research, Hampton House, Room 125, 624 N. Broadway, Baltimore, MD 21205.</note>
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<identifier type="ISSN">0022-1899</identifier>
<identifier type="eISSN">1537-6613</identifier>
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<date>1991</date>
<detail type="volume">
<caption>vol.</caption>
<number>163</number>
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<caption>no.</caption>
<number>5</number>
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<start>1023</start>
<end>1028</end>
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<identifier type="DOI">10.1093/infdis/163.5.1023</identifier>
<accessCondition type="use and reproduction" contentType="copyright">© 1991 by The University of Chicago</accessCondition>
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