An open-label phase I trial of a live attenuated H2N2 influenza virus vaccine in healthy adults.
Identifieur interne : 000148 ( PubMed/Curation ); précédent : 000147; suivant : 000149An open-label phase I trial of a live attenuated H2N2 influenza virus vaccine in healthy adults.
Auteurs : Kawsar R. Talaat [États-Unis] ; Ruth A. Karron ; Philana H. Liang ; Bridget A. Mcmahon ; Catherine J. Luke ; Bhagvanji Thumar ; Grace L. Chen ; Ji-Young Min ; Elaine W. Lamirande ; Hong Jin ; Kathy L. Coelingh ; George W. Kemble ; Kanta SubbaraoSource :
- Influenza and other respiratory viruses [ 1750-2659 ] ; 2013.
Descripteurs français
- KwdFr :
- Adulte, Anticorps antiviraux (sang), Excrétion virale, Femelle, Grippe humaine (), Grippe humaine (immunologie), Grippe humaine (virologie), Humains, Jeune adulte, Mâle, Réplication virale, Résultat thérapeutique, Sous-type H2N2 du virus de la grippe A (génétique), Sous-type H2N2 du virus de la grippe A (immunologie), Sous-type H2N2 du virus de la grippe A (isolement et purification), Sous-type H2N2 du virus de la grippe A (physiologie), Vaccination, Vaccins antigrippaux (administration et posologie), Vaccins antigrippaux (effets indésirables), Vaccins antigrippaux (immunologie), Vaccins atténués (administration et posologie), Vaccins atténués (effets indésirables), Vaccins atténués (immunologie).
- MESH :
- administration et posologie : Vaccins antigrippaux, Vaccins atténués.
- effets indésirables : Vaccins antigrippaux, Vaccins atténués.
- génétique : Sous-type H2N2 du virus de la grippe A.
- immunologie : Grippe humaine, Sous-type H2N2 du virus de la grippe A, Vaccins antigrippaux, Vaccins atténués.
- isolement et purification : Sous-type H2N2 du virus de la grippe A.
- physiologie : Sous-type H2N2 du virus de la grippe A.
- sang : Anticorps antiviraux.
- virologie : Grippe humaine.
- Adulte, Excrétion virale, Femelle, Grippe humaine, Humains, Jeune adulte, Mâle, Réplication virale, Résultat thérapeutique, Vaccination.
English descriptors
- KwdEn :
- Adult, Antibodies, Viral (blood), Female, Humans, Influenza A Virus, H2N2 Subtype (genetics), Influenza A Virus, H2N2 Subtype (immunology), Influenza A Virus, H2N2 Subtype (isolation & purification), Influenza A Virus, H2N2 Subtype (physiology), Influenza Vaccines (administration & dosage), Influenza Vaccines (adverse effects), Influenza Vaccines (immunology), Influenza, Human (immunology), Influenza, Human (prevention & control), Influenza, Human (virology), Male, Treatment Outcome, Vaccination, Vaccines, Attenuated (administration & dosage), Vaccines, Attenuated (adverse effects), Vaccines, Attenuated (immunology), Virus Replication, Virus Shedding, Young Adult.
- MESH :
- chemical , administration & dosage : Influenza Vaccines, Vaccines, Attenuated.
- chemical , adverse effects : Influenza Vaccines, Vaccines, Attenuated.
- chemical , blood : Antibodies, Viral.
- genetics : Influenza A Virus, H2N2 Subtype.
- immunology : Influenza A Virus, H2N2 Subtype, Influenza Vaccines, Influenza, Human, Vaccines, Attenuated.
- isolation & purification : Influenza A Virus, H2N2 Subtype.
- physiology : Influenza A Virus, H2N2 Subtype.
- prevention & control : Influenza, Human.
- virology : Influenza, Human.
- Adult, Female, Humans, Male, Treatment Outcome, Vaccination, Virus Replication, Virus Shedding, Young Adult.
Abstract
Live attenuated influenza vaccines (LAIV) against a variety of strains of pandemic potential are being developed and tested. We describe the results of an open-label phase I trial of a live attenuated H2N2 virus vaccine.
DOI: 10.1111/j.1750-2659.2012.00350.x
PubMed: 22417012
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pubmed:22417012Le document en format XML
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<front><div type="abstract" xml:lang="en">Live attenuated influenza vaccines (LAIV) against a variety of strains of pandemic potential are being developed and tested. We describe the results of an open-label phase I trial of a live attenuated H2N2 virus vaccine.</div>
</front>
</TEI>
<pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">22417012</PMID>
<DateCompleted><Year>2013</Year>
<Month>06</Month>
<Day>14</Day>
</DateCompleted>
<DateRevised><Year>2018</Year>
<Month>11</Month>
<Day>13</Day>
</DateRevised>
<Article PubModel="Print-Electronic"><Journal><ISSN IssnType="Electronic">1750-2659</ISSN>
<JournalIssue CitedMedium="Internet"><Volume>7</Volume>
<Issue>1</Issue>
<PubDate><Year>2013</Year>
<Month>Jan</Month>
</PubDate>
</JournalIssue>
<Title>Influenza and other respiratory viruses</Title>
<ISOAbbreviation>Influenza Other Respir Viruses</ISOAbbreviation>
</Journal>
<ArticleTitle>An open-label phase I trial of a live attenuated H2N2 influenza virus vaccine in healthy adults.</ArticleTitle>
<Pagination><MedlinePgn>66-73</MedlinePgn>
</Pagination>
<ELocationID EIdType="doi" ValidYN="Y">10.1111/j.1750-2659.2012.00350.x</ELocationID>
<Abstract><AbstractText Label="BACKGROUND" NlmCategory="BACKGROUND">Live attenuated influenza vaccines (LAIV) against a variety of strains of pandemic potential are being developed and tested. We describe the results of an open-label phase I trial of a live attenuated H2N2 virus vaccine.</AbstractText>
<AbstractText Label="OBJECTIVES" NlmCategory="OBJECTIVE">To evaluate the safety, infectivity, and immunogenicity of a live attenuated H2N2 influenza virus vaccine.</AbstractText>
<AbstractText Label="PARTICIPANTS/METHODS" NlmCategory="METHODS">The A/Ann Arbor/6/60 (H2N2) virus used in this study is the attenuated, cold-adapted, temperature-sensitive strain that provides the genetic backbone of seasonal LAIV (MedImmune). We evaluated the safety, infectivity, and immunogenicity of two doses of 10(7) TCID(50) of this vaccine administered by nasal spray 4 weeks apart to normal healthy seronegative adults.</AbstractText>
<AbstractText Label="RESULTS" NlmCategory="RESULTS">Twenty-one participants received a first dose of the vaccine; 18 participants received a second dose. No serious adverse events occurred during the trial. The most common adverse events after vaccination were headache and musculoskeletal pain. The vaccine was restricted in replication: 24% and 17% had virus detectable by culture or rRT-PCR after the first and second dose, respectively. Antibody responses to the vaccine were also restricted: 24% of participants developed an antibody response as measured by either hemagglutination-inhibition assay (10%), or ELISA for H2 HA-specific serum IgG (24%) or IgA (16%) after either one or two doses. None of the participants had a neutralizing antibody response. Vaccine-specific IgG-secreting cells as measured by enzyme-linked immunospot increased from a mean of 0·5 to 2·0/10(6) peripheral blood mononuclear cells (PBMCs); vaccine-specific IgA-secreting cells increased from 0·1 to 0·5/10(6) PBMCs.</AbstractText>
<AbstractText Label="CONCLUSIONS" NlmCategory="CONCLUSIONS">The live attenuated H2N2 1960 AA ca vaccine demonstrated a safety profile consistent with seasonal trivalent LAIV but was restricted in replication and minimally immunogenic in healthy seronegative adults.</AbstractText>
<CopyrightInformation>Published 2012. This article is a US Government work and is in the public domain in the USA.</CopyrightInformation>
</Abstract>
<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Talaat</LastName>
<ForeName>Kawsar R</ForeName>
<Initials>KR</Initials>
<AffiliationInfo><Affiliation>Center for Immunization Research, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, USA.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Karron</LastName>
<ForeName>Ruth A</ForeName>
<Initials>RA</Initials>
</Author>
<Author ValidYN="Y"><LastName>Liang</LastName>
<ForeName>Philana H</ForeName>
<Initials>PH</Initials>
</Author>
<Author ValidYN="Y"><LastName>McMahon</LastName>
<ForeName>Bridget A</ForeName>
<Initials>BA</Initials>
</Author>
<Author ValidYN="Y"><LastName>Luke</LastName>
<ForeName>Catherine J</ForeName>
<Initials>CJ</Initials>
</Author>
<Author ValidYN="Y"><LastName>Thumar</LastName>
<ForeName>Bhagvanji</ForeName>
<Initials>B</Initials>
</Author>
<Author ValidYN="Y"><LastName>Chen</LastName>
<ForeName>Grace L</ForeName>
<Initials>GL</Initials>
</Author>
<Author ValidYN="Y"><LastName>Min</LastName>
<ForeName>Ji-Young</ForeName>
<Initials>JY</Initials>
</Author>
<Author ValidYN="Y"><LastName>Lamirande</LastName>
<ForeName>Elaine W</ForeName>
<Initials>EW</Initials>
</Author>
<Author ValidYN="Y"><LastName>Jin</LastName>
<ForeName>Hong</ForeName>
<Initials>H</Initials>
</Author>
<Author ValidYN="Y"><LastName>Coelingh</LastName>
<ForeName>Kathy L</ForeName>
<Initials>KL</Initials>
</Author>
<Author ValidYN="Y"><LastName>Kemble</LastName>
<ForeName>George W</ForeName>
<Initials>GW</Initials>
</Author>
<Author ValidYN="Y"><LastName>Subbarao</LastName>
<ForeName>Kanta</ForeName>
<Initials>K</Initials>
</Author>
</AuthorList>
<Language>eng</Language>
<GrantList CompleteYN="Y"><Grant><GrantID>N01 AI015444</GrantID>
<Acronym>AI</Acronym>
<Agency>NIAID NIH HHS</Agency>
<Country>United States</Country>
</Grant>
<Grant><Agency>Intramural NIH HHS</Agency>
<Country>United States</Country>
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<ArticleDate DateType="Electronic"><Year>2012</Year>
<Month>03</Month>
<Day>14</Day>
</ArticleDate>
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<MedlineTA>Influenza Other Respir Viruses</MedlineTA>
<NlmUniqueID>101304007</NlmUniqueID>
<ISSNLinking>1750-2640</ISSNLinking>
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