A Live Attenuated Influenza A(H5N1) Vaccine Induces Long-Term Immunity in the Absence of a Primary Antibody Response

Background. Highly pathogenic avian influenza A(H5N1) causes severe infections in humans. We generated 2 influenza A(H5N1) live attenuated influenza vaccines for pandemic use (pLAIVs), but they failed to elicit a primary immune response. Our objective was to determine whether the vaccines primed or...

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Published inThe Journal of infectious diseases Vol. 209; no. 12; pp. 1860 - 1869
Main Authors Talaat, Kawsar R., Luke, Catherine J., Khurana, Surender, Manischewitz, Jody, King, Lisa R., McMahon, Bridget A., Karron, Ruth A., Lewis, Kristen D. C., Qin, Jing, Follmann, Dean A., Golding, Hana, Neuzil, Kathleen M., Subbarao, Kanta
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Published Oxford Oxford University Press 15.06.2014
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Abstract Background. Highly pathogenic avian influenza A(H5N1) causes severe infections in humans. We generated 2 influenza A(H5N1) live attenuated influenza vaccines for pandemic use (pLAIVs), but they failed to elicit a primary immune response. Our objective was to determine whether the vaccines primed or established long-lasting immunity that could be detected by administration of inactivated subvirion influenza A(H5N1) vaccine (ISIV). Methods. The following groups were invited to participate in the study: persons who previously received influenza A(H5N1) pLAIV; persons who previously received an irrelevant influenza A(H7N3) pLAIV; and community members who were naive to influenza A(H5N1) and LAIV. LAIV-experienced subjects received a single 45-ug dose of influenza A(H5N1) ISIV. Influenza A(H5N1)-and LAIV-naive subjects received either 1 or 2 doses of ISIV. Results. In subjects who had previously received antigenically matched influenza A(H5N1) pLAIV followed by 1 dose of ISIV compared with those who were naive to influenza A(H5N1) and LAIV and received 2 doses of ISIV, we observed an increased frequency of antibody response (82% vs 50%, by the hemagglutination inhibition assay) and a significantly higher antibody titer (112 vs 76; P = .04). The affinity of antibody and breadth of cross-dade neutralization was also enhanced in influenza A(H5N1) pLAIV-primed subjects. Conclusions. ISIV administration unmasked long-lasting immunity in influenza A(H5N1) pLAIV recipients, with a rapid, high-titer, high-quality antibody response that was broadly cross-reactive across several influenza A(H5N1) clades.
AbstractList Background.  Highly pathogenic avian influenza A(H5N1) causes severe infections in humans. We generated 2 influenza A(H5N1) live attenuated influenza vaccines for pandemic use (pLAIVs), but they failed to elicit a primary immune response. Our objective was to determine whether the vaccines primed or established long-lasting immunity that could be detected by administration of inactivated subvirion influenza A(H5N1) vaccine (ISIV). Methods.  The following groups were invited to participate in the study: persons who previously received influenza A(H5N1) pLAIV; persons who previously received an irrelevant influenza A(H7N3) pLAIV; and community members who were naive to influenza A(H5N1) and LAIV. LAIV-experienced subjects received a single 45-μg dose of influenza A(H5N1) ISIV. Influenza A(H5N1)– and LAIV-naive subjects received either 1 or 2 doses of ISIV. Results.  In subjects who had previously received antigenically matched influenza A(H5N1) pLAIV followed by 1 dose of ISIV compared with those who were naive to influenza A(H5N1) and LAIV and received 2 doses of ISIV, we observed an increased frequency of antibody response (82% vs 50%, by the hemagglutination inhibition assay) and a significantly higher antibody titer (112 vs 76; P = .04). The affinity of antibody and breadth of cross-clade neutralization was also enhanced in influenza A(H5N1) pLAIV–primed subjects. Conclusions.  ISIV administration unmasked long-lasting immunity in influenza A(H5N1) pLAIV recipients, with a rapid, high-titer, high-quality antibody response that was broadly cross-reactive across several influenza A(H5N1) clades. Clinical Trials Registration.  NCT01109329.
Background. Highly pathogenic avian influenza A(H5N1) causes severe infections in humans. We generated 2 influenza A(H5N1) live attenuated influenza vaccines for pandemic use (pLAIVs), but they failed to elicit a primary immune response. Our objective was to determine whether the vaccines primed or established long-lasting immunity that could be detected by administration of inactivated subvirion influenza A(H5N1) vaccine (ISIV). Methods. The following groups were invited to participate in the study: persons who previously received influenza A(H5N1) pLAIV; persons who previously received an irrelevant influenza A(H7N3) pLAIV; and community members who were naive to influenza A(H5N1) and LAIV. LAIV-experienced subjects received a single 45- mu g dose of influenza A(H5N1) ISIV. Influenza A(H5N1)- and LAIV-naive subjects received either 1 or 2 doses of ISIV. Results. In subjects who had previously received antigenically matched influenza A(H5N1) pLAIV followed by 1 dose of ISIV compared with those who were naive to influenza A(H5N1) and LAIV and received 2 doses of ISIV, we observed an increased frequency of antibody response (82% vs 50%, by the hemagglutination inhibition assay) and a significantly higher antibody titer (112 vs 76; P = .04). The affinity of antibody and breadth of cross-clade neutralization was also enhanced in influenza A(H5N1) pLAIV-primed subjects. Conclusions. ISIV administration unmasked long-lasting immunity in influenza A(H5N1) pLAIV recipients, with a rapid, high-titer, high-quality antibody response that was broadly cross-reactive across several influenza A(H5N1) clades.
Background. Highly pathogenic avian influenza A(H5N1) causes severe infections in humans. We generated 2 influenza A(H5N1) live attenuated influenza vaccines for pandemic use (pLAIVs), but they failed to elicit a primary immune response. Our objective was to determine whether the vaccines primed or established long-lasting immunity that could be detected by administration of inactivated subvirion influenza A(H5N1) vaccine (ISIV). Methods. The following groups were invited to participate in the study: persons who previously received influenza A(H5N1) pLAIV; persons who previously received an irrelevant influenza A(H7N3) pLAIV; and community members who were naive to influenza A(H5N1) and LAIV. LAIV-experienced subjects received a single 45-ug dose of influenza A(H5N1) ISIV. Influenza A(H5N1)-and LAIV-naive subjects received either 1 or 2 doses of ISIV. Results. In subjects who had previously received antigenically matched influenza A(H5N1) pLAIV followed by 1 dose of ISIV compared with those who were naive to influenza A(H5N1) and LAIV and received 2 doses of ISIV, we observed an increased frequency of antibody response (82% vs 50%, by the hemagglutination inhibition assay) and a significantly higher antibody titer (112 vs 76; P = .04). The affinity of antibody and breadth of cross-dade neutralization was also enhanced in influenza A(H5N1) pLAIV-primed subjects. Conclusions. ISIV administration unmasked long-lasting immunity in influenza A(H5N1) pLAIV recipients, with a rapid, high-titer, high-quality antibody response that was broadly cross-reactive across several influenza A(H5N1) clades.
Highly pathogenic avian influenza A(H5N1) causes severe infections in humans. We generated 2 influenza A(H5N1) live attenuated influenza vaccines for pandemic use (pLAIVs), but they failed to elicit a primary immune response. Our objective was to determine whether the vaccines primed or established long-lasting immunity that could be detected by administration of inactivated subvirion influenza A(H5N1) vaccine (ISIV).BACKGROUNDHighly pathogenic avian influenza A(H5N1) causes severe infections in humans. We generated 2 influenza A(H5N1) live attenuated influenza vaccines for pandemic use (pLAIVs), but they failed to elicit a primary immune response. Our objective was to determine whether the vaccines primed or established long-lasting immunity that could be detected by administration of inactivated subvirion influenza A(H5N1) vaccine (ISIV).The following groups were invited to participate in the study: persons who previously received influenza A(H5N1) pLAIV; persons who previously received an irrelevant influenza A(H7N3) pLAIV; and community members who were naive to influenza A(H5N1) and LAIV. LAIV-experienced subjects received a single 45-μg dose of influenza A(H5N1) ISIV. Influenza A(H5N1)- and LAIV-naive subjects received either 1 or 2 doses of ISIV.METHODSThe following groups were invited to participate in the study: persons who previously received influenza A(H5N1) pLAIV; persons who previously received an irrelevant influenza A(H7N3) pLAIV; and community members who were naive to influenza A(H5N1) and LAIV. LAIV-experienced subjects received a single 45-μg dose of influenza A(H5N1) ISIV. Influenza A(H5N1)- and LAIV-naive subjects received either 1 or 2 doses of ISIV.In subjects who had previously received antigenically matched influenza A(H5N1) pLAIV followed by 1 dose of ISIV compared with those who were naive to influenza A(H5N1) and LAIV and received 2 doses of ISIV, we observed an increased frequency of antibody response (82% vs 50%, by the hemagglutination inhibition assay) and a significantly higher antibody titer (112 vs 76; P = .04). The affinity of antibody and breadth of cross-clade neutralization was also enhanced in influenza A(H5N1) pLAIV-primed subjects.RESULTSIn subjects who had previously received antigenically matched influenza A(H5N1) pLAIV followed by 1 dose of ISIV compared with those who were naive to influenza A(H5N1) and LAIV and received 2 doses of ISIV, we observed an increased frequency of antibody response (82% vs 50%, by the hemagglutination inhibition assay) and a significantly higher antibody titer (112 vs 76; P = .04). The affinity of antibody and breadth of cross-clade neutralization was also enhanced in influenza A(H5N1) pLAIV-primed subjects.ISIV administration unmasked long-lasting immunity in influenza A(H5N1) pLAIV recipients, with a rapid, high-titer, high-quality antibody response that was broadly cross-reactive across several influenza A(H5N1) clades.CONCLUSIONSISIV administration unmasked long-lasting immunity in influenza A(H5N1) pLAIV recipients, with a rapid, high-titer, high-quality antibody response that was broadly cross-reactive across several influenza A(H5N1) clades.NCT01109329.CLINICAL TRIALS REGISTRATIONNCT01109329.
Highly pathogenic avian influenza A(H5N1) causes severe infections in humans. We generated 2 influenza A(H5N1) live attenuated influenza vaccines for pandemic use (pLAIVs), but they failed to elicit a primary immune response. Our objective was to determine whether the vaccines primed or established long-lasting immunity that could be detected by administration of inactivated subvirion influenza A(H5N1) vaccine (ISIV). The following groups were invited to participate in the study: persons who previously received influenza A(H5N1) pLAIV; persons who previously received an irrelevant influenza A(H7N3) pLAIV; and community members who were naive to influenza A(H5N1) and LAIV. LAIV-experienced subjects received a single 45-μg dose of influenza A(H5N1) ISIV. Influenza A(H5N1)- and LAIV-naive subjects received either 1 or 2 doses of ISIV. In subjects who had previously received antigenically matched influenza A(H5N1) pLAIV followed by 1 dose of ISIV compared with those who were naive to influenza A(H5N1) and LAIV and received 2 doses of ISIV, we observed an increased frequency of antibody response (82% vs 50%, by the hemagglutination inhibition assay) and a significantly higher antibody titer (112 vs 76; P = .04). The affinity of antibody and breadth of cross-clade neutralization was also enhanced in influenza A(H5N1) pLAIV-primed subjects. ISIV administration unmasked long-lasting immunity in influenza A(H5N1) pLAIV recipients, with a rapid, high-titer, high-quality antibody response that was broadly cross-reactive across several influenza A(H5N1) clades. NCT01109329.
Author Luke, Catherine J.
Khurana, Surender
Subbarao, Kanta
Lewis, Kristen D. C.
King, Lisa R.
McMahon, Bridget A.
Qin, Jing
Manischewitz, Jody
Karron, Ruth A.
Neuzil, Kathleen M.
Talaat, Kawsar R.
Golding, Hana
Follmann, Dean A.
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  surname: Subbarao
  fullname: Subbarao, Kanta
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https://www.ncbi.nlm.nih.gov/pubmed/24604819$$D View this record in MEDLINE/PubMed
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Cites_doi 10.1016/S0022-3476(00)70097-7
10.1097/01.inf.0000143643.44463.b1
10.1371/journal.pone.0021942
10.1016/j.vaccine.2009.03.082
10.1086/595832
10.1126/science.1171491
10.1016/S0140-6736(00)05066-2
10.1086/596558
10.1016/j.vaccine.2011.02.043
10.1016/j.virusres.2013.05.006
10.1128/JCM.37.4.937-943.1999
10.1016/j.vaccine.2008.05.077
10.1172/JCI41902
10.1056/NEJMoa055778
10.1016/S0264-410X(02)00632-1
10.1016/j.virusres.2004.02.019
10.1086/605608
10.1016/j.vaccine.2009.10.152
10.1126/science.279.5349.393
10.1128/JCM.23.2.240-245.1986
10.1016/S1473-3099(12)70345-6
10.1016/S0264-410X(00)00395-9
10.1126/scitranslmed.3005191
10.1016/j.vaccine.2009.05.099
10.1093/infdis/jit178
10.1093/infdis/jit180
10.1128/JVI.02107-10
10.1371/journal.pmed.0030360
10.1111/j.1750-2659.2012.00350.x
10.1086/526537
10.1016/S1473-3099(11)70240-7
10.1086/590916
10.1038/nsmb.1566
10.1371/journal.pone.0011548
ContentType Journal Article
Copyright Copyright © 2014 Oxford University Press on behalf of the Infectious Diseases Society of America
2015 INIST-CNRS
Published by Oxford University Press on behalf of the Infectious Diseases Society of America 2014. This work is written by (a) US Government employee(s) and is in the public domain in the US.
Published by Oxford University Press on behalf of the Infectious Diseases Society of America 2014. This work is written by (a) US Government employee(s) and is in the public domain in the US. 2014
Copyright_xml – notice: Copyright © 2014 Oxford University Press on behalf of the Infectious Diseases Society of America
– notice: 2015 INIST-CNRS
– notice: Published by Oxford University Press on behalf of the Infectious Diseases Society of America 2014. This work is written by (a) US Government employee(s) and is in the public domain in the US.
– notice: Published by Oxford University Press on behalf of the Infectious Diseases Society of America 2014. This work is written by (a) US Government employee(s) and is in the public domain in the US. 2014
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ISSN 0022-1899
1537-6613
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IsDoiOpenAccess false
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Issue 12
Keywords Virus
Infection
Influenzavirus A
Immune response
Influenza A virus
Viral disease
Orthomyxoviridae
Influenza A
Vaccine
Attenuated strain
Humoral immunity
live attenuated
H5N1
vaccine
avian influenza
Language English
License CC BY 4.0
Published by Oxford University Press on behalf of the Infectious Diseases Society of America 2014. This work is written by (a) US Government employee(s) and is in the public domain in the US.
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content type line 23
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K. T. and C. L. contributed equally to this work
Presented in part: World Health Organization Integrated Meeting on Development and Clinical Trials of Influenza Vaccines That Induce Broadly Protective and Long-Lasting Immune Responses, Hong Kong SAR, China, 22–27 January 2013; Options for the Control of Influenza VIII; Cape Town, South Africa, 5–9 September 2013. Abstract O-859.
Present affiliation: SNBL Clinical Pharmacology Center, Baltimore, Maryland.
OpenAccessLink https://academic.oup.com/jid/article-pdf/209/12/1860/18069834/jiu123.pdf
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References Khurana ( key 20170702155307_JIU123C24) 2013; 208
Lin ( key 20170702155307_JIU123C28) 2009; 199
Talaat ( key 20170702155307_JIU123C18) 2012; 7
Ledgerwood ( key 20170702155307_JIU123C12) 2011; 11
Mendelman ( key 20170702155307_JIU123C5) 2004; 23
World Health Organization ( key 20170702155307_JIU123C2)
Patel ( key 20170702155307_JIU123C31) 2010; 28
Sui ( key 20170702155307_JIU123C34) 2009; 16
Suguitan ( key 20170702155307_JIU123C9) 2011; 6
Gurwith ( key 20170702155307_JIU123C11) 2013; 13
Khurana ( key 20170702155307_JIU123C26) 2011; 85
Rowe ( key 20170702155307_JIU123C22) 1999; 37
Zangwill ( key 20170702155307_JIU123C30) 2008; 197
Subbarao ( key 20170702155307_JIU123C1) 1998; 279
Ehrlich ( key 20170702155307_JIU123C27) 2009; 200
Karron ( key 20170702155307_JIU123C7) 2009; 27
Talaat ( key 20170702155307_JIU123C19) 2011; 29
Stephenson ( key 20170702155307_JIU123C15) 2003; 21
Nicholson ( key 20170702155307_JIU123C14) 2001; 357
Corti ( key 20170702155307_JIU123C32) 2010; 120
Belshe ( key 20170702155307_JIU123C4) 2000; 136
Baz ( key 20170702155307_JIU123C3) 2013; 178
Ledgerwood ( key 20170702155307_JIU123C13) 2013; 208
Ekiert ( key 20170702155307_JIU123C33) 2009; 324
Walls ( key 20170702155307_JIU123C23) 1986; 23
Treanor ( key 20170702155307_JIU123C8) 2006; 354
Talaat ( key 20170702155307_JIU123C17) 2009; 27
Karron ( key 20170702155307_JIU123C20) 2009; 199
Stephenson ( key 20170702155307_JIU123C21) 2004; 103
Khurana ( key 20170702155307_JIU123C25) 2010; 5
Bentebibel ( key 20170702155307_JIU123C35) 2013; 5
Treanor ( key 20170702155307_JIU123C16) 2001; 19
Nolan ( key 20170702155307_JIU123C29) 2008; 26
Suguitan ( key 20170702155307_JIU123C6) 2006; 3
Goji ( key 20170702155307_JIU123C10) 2008; 198
19464558 - Vaccine. 2009 Jun 8;27(28):3744-53
19540952 - Vaccine. 2009 Aug 6;27(36):4953-60
21760928 - PLoS One. 2011;6(7):e21942
23369412 - Lancet Infect Dis. 2013 Mar;13(3):238-50
9430591 - Science. 1998 Jan 16;279(5349):393-6
19251591 - Science. 2009 Apr 10;324(5924):246-51
19067606 - J Infect Dis. 2009 Jan 15;199(2):184-7
21084473 - J Virol. 2011 Feb;85(3):1246-56
21975270 - Lancet Infect Dis. 2011 Dec;11(12):916-24
24604818 - J Infect Dis. 2014 Jun 15;209(12):1857-9
19210163 - J Infect Dis. 2009 Mar 1;199(5):711-6
16571878 - N Engl J Med. 2006 Mar 30;354(13):1343-51
23486778 - Sci Transl Med. 2013 Mar 13;5(176):176ra32
23726847 - Virus Res. 2013 Dec 5;178(1):78-98
10657821 - J Pediatr. 2000 Feb;136(2):168-75
18237269 - J Infect Dis. 2008 Feb 15;197(4):580-3
11166898 - Vaccine. 2001 Feb 8;19(13-14):1732-7
12639491 - Vaccine. 2003 Apr 2;21(15):1687-93
19234466 - Nat Struct Mol Biol. 2009 Mar;16(3):265-73
23633407 - J Infect Dis. 2013 Aug 1;208(3):418-22
15163495 - Virus Res. 2004 Jul;103(1-2):91-5
11425416 - Lancet. 2001 Jun 16;357(9272):1937-43
10074505 - J Clin Microbiol. 1999 Apr;37(4):937-43
20389023 - J Clin Invest. 2010 May;120(5):1663-73
16968127 - PLoS Med. 2006 Sep;3(9):e360
18694338 - J Infect Dis. 2008 Sep 1;198(5):635-41
18599164 - Vaccine. 2008 Aug 5;26(33):4160-7
19712040 - J Infect Dis. 2009 Oct 1;200(7):1113-8
20634959 - PLoS One. 2010;5(7):e11548
3517049 - J Clin Microbiol. 1986 Feb;23(2):240-5
19931380 - Vaccine. 2010 Apr 9;28(17):3025-9
15545863 - Pediatr Infect Dis J. 2004 Nov;23(11):1053-5
23633404 - J Infect Dis. 2013 Aug 1;208(3):413-7
J Infect Dis. 2014 Dec 15;210(12):2021
22417012 - Influenza Other Respir Viruses. 2013 Jan;7(1):66-73
21377509 - Vaccine. 2011 Apr 12;29(17):3144-8
References_xml – volume: 136
  start-page: 168
  year: 2000
  ident: key 20170702155307_JIU123C4
  article-title: Efficacy of vaccination with live attenuated, cold-adapted, trivalent, intranasal influenza virus vaccine against a variant (A/Sydney) not contained in the vaccine
  publication-title: J Pediatr
  doi: 10.1016/S0022-3476(00)70097-7
– volume: 23
  start-page: 1053
  year: 2004
  ident: key 20170702155307_JIU123C5
  article-title: Live attenuated influenza vaccine induces cross-reactive antibody responses in children against an A/Fujian/411/2002-like H3N2 antigenic variant strain
  publication-title: Pediatr Infect Dis J
  doi: 10.1097/01.inf.0000143643.44463.b1
– volume: 6
  start-page: e21942
  year: 2011
  ident: key 20170702155307_JIU123C9
  article-title: Influenza H5 hemagglutinin DNA primes the antibody response elicited by the live attenuated influenza A/Vietnam/1203/2004 vaccine in ferrets
  publication-title: PLoS One
  doi: 10.1371/journal.pone.0021942
– volume: 27
  start-page: 3744
  year: 2009
  ident: key 20170702155307_JIU123C17
  article-title: A live attenuated H7N3 influenza virus vaccine is well tolerated and immunogenic in a Phase I trial in healthy adults
  publication-title: Vaccine
  doi: 10.1016/j.vaccine.2009.03.082
– volume: 199
  start-page: 184
  year: 2009
  ident: key 20170702155307_JIU123C28
  article-title: Antibody persistence after 2-dose priming and booster response to a third dose of an inactivated, adjuvanted, whole-virion H5N1 vaccine
  publication-title: J Infect Dis
  doi: 10.1086/595832
– volume: 324
  start-page: 246
  year: 2009
  ident: key 20170702155307_JIU123C33
  article-title: Antibody recognition of a highly conserved influenza virus epitope
  publication-title: Science
  doi: 10.1126/science.1171491
– volume: 357
  start-page: 1937
  year: 2001
  ident: key 20170702155307_JIU123C14
  article-title: Safety and antigenicity of non-adjuvanted and MF59-adjuvanted influenza A/Duck/Singapore/97 (H5N3) vaccine: a randomised trial of two potential vaccines against H5N1 influenza
  publication-title: Lancet
  doi: 10.1016/S0140-6736(00)05066-2
– volume: 199
  start-page: 711
  year: 2009
  ident: key 20170702155307_JIU123C20
  article-title: A live attenuated H9N2 influenza vaccine is well tolerated and immunogenic in healthy adults
  publication-title: J Infect Dis
  doi: 10.1086/596558
– volume: 29
  start-page: 3144
  year: 2011
  ident: key 20170702155307_JIU123C19
  article-title: An open label phase I trial of a live attenuated H6N1 influenza virus vaccine in healthy adults
  publication-title: Vaccine
  doi: 10.1016/j.vaccine.2011.02.043
– volume: 178
  start-page: 78
  year: 2013
  ident: key 20170702155307_JIU123C3
  article-title: H5N1 vaccines in humans
  publication-title: Virus Res
  doi: 10.1016/j.virusres.2013.05.006
– volume: 37
  start-page: 937
  year: 1999
  ident: key 20170702155307_JIU123C22
  article-title: Detection of antibody to avian influenza A (H5N1) virus in human serum by using a combination of serologic assays
  publication-title: J Clin Microbiol
  doi: 10.1128/JCM.37.4.937-943.1999
– volume: 26
  start-page: 4160
  year: 2008
  ident: key 20170702155307_JIU123C29
  article-title: Phase I and II randomised trials of the safety and immunogenicity of a prototype adjuvanted inactivated split-virus influenza A (H5N1) vaccine in healthy adults
  publication-title: Vaccine
  doi: 10.1016/j.vaccine.2008.05.077
– volume: 120
  start-page: 1663
  year: 2010
  ident: key 20170702155307_JIU123C32
  article-title: Heterosubtypic neutralizing antibodies are produced by individuals immunized with a seasonal influenza vaccine
  publication-title: J Clin Invest
  doi: 10.1172/JCI41902
– volume: 354
  start-page: 1343
  year: 2006
  ident: key 20170702155307_JIU123C8
  article-title: Safety and immunogenicity of an inactivated subvirion influenza A (H5N1) vaccine
  publication-title: N Engl J Med
  doi: 10.1056/NEJMoa055778
– volume: 21
  start-page: 1687
  year: 2003
  ident: key 20170702155307_JIU123C15
  article-title: Boosting immunity to influenza H5N1 with MF59-adjuvanted H5N3 A/Duck/Singapore/97 vaccine in a primed human population
  publication-title: Vaccine
  doi: 10.1016/S0264-410X(02)00632-1
– volume: 103
  start-page: 91
  year: 2004
  ident: key 20170702155307_JIU123C21
  article-title: Detection of anti-H5 responses in human sera by HI using horse erythrocytes following MF59-adjuvanted influenza A/Duck/Singapore/97 vaccine
  publication-title: Virus Res
  doi: 10.1016/j.virusres.2004.02.019
– volume: 200
  start-page: 1113
  year: 2009
  ident: key 20170702155307_JIU123C27
  article-title: A cell culture (Vero)-derived H5N1 whole-virus vaccine induces cross-reactive memory responses
  publication-title: J Infect Dis
  doi: 10.1086/605608
– volume: 28
  start-page: 3025
  year: 2010
  ident: key 20170702155307_JIU123C31
  article-title: A phase I evaluation of inactivated influenza A/H5N1 vaccine administered by the intradermal or the intramuscular route
  publication-title: Vaccine
  doi: 10.1016/j.vaccine.2009.10.152
– volume: 279
  start-page: 393
  year: 1998
  ident: key 20170702155307_JIU123C1
  article-title: Characterization of an avian influenza A (H5N1) virus isolated from a child with a fatal respiratory illness
  publication-title: Science
  doi: 10.1126/science.279.5349.393
– ident: key 20170702155307_JIU123C2
  article-title: Cumulative number of confirmed human cases of avian influenza A(H5N1) reported to WHO.
– volume: 23
  start-page: 240
  year: 1986
  ident: key 20170702155307_JIU123C23
  article-title: Characterization and evaluation of monoclonal antibodies developed for typing influenza A and influenza B viruses
  publication-title: J Clin Microbiol
  doi: 10.1128/JCM.23.2.240-245.1986
– volume: 13
  start-page: 238
  year: 2013
  ident: key 20170702155307_JIU123C11
  article-title: Safety and immunogenicity of an oral, replicating adenovirus serotype 4 vector vaccine for H5N1 influenza: a randomised, double-blind, placebo-controlled, phase 1 study
  publication-title: Lancet Infect Dis
  doi: 10.1016/S1473-3099(12)70345-6
– volume: 19
  start-page: 1732
  year: 2001
  ident: key 20170702155307_JIU123C16
  article-title: Safety and immunogenicity of a recombinant hemagglutinin vaccine for H5 influenza in humans
  publication-title: Vaccine
  doi: 10.1016/S0264-410X(00)00395-9
– volume: 5
  start-page: 176ra32
  year: 2013
  ident: key 20170702155307_JIU123C35
  article-title: Induction of ICOS+CXCR3+CXCR5+ TH cells correlates with antibody responses to influenza vaccination
  publication-title: Sci Transl Med
  doi: 10.1126/scitranslmed.3005191
– volume: 27
  start-page: 4953
  year: 2009
  ident: key 20170702155307_JIU123C7
  article-title: Evaluation of two live attenuated cold-adapted H5N1 influenza virus vaccines in healthy adults
  publication-title: Vaccine
  doi: 10.1016/j.vaccine.2009.05.099
– volume: 208
  start-page: 413
  year: 2013
  ident: key 20170702155307_JIU123C24
  article-title: DNA priming prior to H5N1 inactivated influenza vaccination expands antibody epitope repertoire and increases affinity maturation in a boost-interval-dependent manner in adults
  publication-title: J Infect Dis
  doi: 10.1093/infdis/jit178
– volume: 208
  start-page: 418
  year: 2013
  ident: key 20170702155307_JIU123C13
  article-title: Prime-boost interval matters: a randomized phase I study to identify the minimum interval necessary to observe the H5 DNA influenza vaccine priming effect
  publication-title: J Infect Dis
  doi: 10.1093/infdis/jit180
– volume: 85
  start-page: 1246
  year: 2011
  ident: key 20170702155307_JIU123C26
  article-title: Bacterial HA1 vaccine against pandemic H5N1 influenza virus: evidence of oligomerization, hemagglutination, and cross-protective immunity in ferrets
  publication-title: J Virol
  doi: 10.1128/JVI.02107-10
– volume: 3
  start-page: e360
  year: 2006
  ident: key 20170702155307_JIU123C6
  article-title: Live, attenuated influenza A H5N1 candidate vaccines provide broad cross-protection in mice and ferrets
  publication-title: PLoS Med
  doi: 10.1371/journal.pmed.0030360
– volume: 7
  start-page: 66
  year: 2012
  ident: key 20170702155307_JIU123C18
  article-title: An open-label phase I trial of a live attenuated H2N2 influenza virus vaccine in healthy adults
  publication-title: Influenza Other Respi Viruses
  doi: 10.1111/j.1750-2659.2012.00350.x
– volume: 197
  start-page: 580
  year: 2008
  ident: key 20170702155307_JIU123C30
  article-title: Evaluation of the safety and immunogenicity of a booster (third) dose of inactivated subvirion H5N1 influenza vaccine in humans
  publication-title: J Infect Dis
  doi: 10.1086/526537
– volume: 11
  start-page: 916
  year: 2011
  ident: key 20170702155307_JIU123C12
  article-title: DNA priming and influenza vaccine immunogenicity: two phase 1 open label randomised clinical trials
  publication-title: Lancet Infect Dis
  doi: 10.1016/S1473-3099(11)70240-7
– volume: 198
  start-page: 635
  year: 2008
  ident: key 20170702155307_JIU123C10
  article-title: Immune responses of healthy subjects to a single dose of intramuscular inactivated influenza A/Vietnam/1203/2004 (H5N1) vaccine after priming with an antigenic variant
  publication-title: J Infect Dis
  doi: 10.1086/590916
– volume: 16
  start-page: 265
  year: 2009
  ident: key 20170702155307_JIU123C34
  article-title: Structural and functional bases for broad-spectrum neutralization of avian and human influenza A viruses
  publication-title: Nat Struct Mol Biol
  doi: 10.1038/nsmb.1566
– volume: 5
  start-page: e11548
  year: 2010
  ident: key 20170702155307_JIU123C25
  article-title: Properly folded bacterially expressed H1N1 hemagglutinin globular head and ectodomain vaccines protect ferrets against H1N1 pandemic influenza virus
  publication-title: PLoS One
  doi: 10.1371/journal.pone.0011548
– reference: 19067606 - J Infect Dis. 2009 Jan 15;199(2):184-7
– reference: 19464558 - Vaccine. 2009 Jun 8;27(28):3744-53
– reference: 22417012 - Influenza Other Respir Viruses. 2013 Jan;7(1):66-73
– reference: - J Infect Dis. 2014 Dec 15;210(12):2021
– reference: 16571878 - N Engl J Med. 2006 Mar 30;354(13):1343-51
– reference: 24604818 - J Infect Dis. 2014 Jun 15;209(12):1857-9
– reference: 23633404 - J Infect Dis. 2013 Aug 1;208(3):413-7
– reference: 16968127 - PLoS Med. 2006 Sep;3(9):e360
– reference: 21084473 - J Virol. 2011 Feb;85(3):1246-56
– reference: 15545863 - Pediatr Infect Dis J. 2004 Nov;23(11):1053-5
– reference: 21975270 - Lancet Infect Dis. 2011 Dec;11(12):916-24
– reference: 19210163 - J Infect Dis. 2009 Mar 1;199(5):711-6
– reference: 3517049 - J Clin Microbiol. 1986 Feb;23(2):240-5
– reference: 19540952 - Vaccine. 2009 Aug 6;27(36):4953-60
– reference: 11425416 - Lancet. 2001 Jun 16;357(9272):1937-43
– reference: 18599164 - Vaccine. 2008 Aug 5;26(33):4160-7
– reference: 21377509 - Vaccine. 2011 Apr 12;29(17):3144-8
– reference: 10074505 - J Clin Microbiol. 1999 Apr;37(4):937-43
– reference: 15163495 - Virus Res. 2004 Jul;103(1-2):91-5
– reference: 20634959 - PLoS One. 2010;5(7):e11548
– reference: 23486778 - Sci Transl Med. 2013 Mar 13;5(176):176ra32
– reference: 23633407 - J Infect Dis. 2013 Aug 1;208(3):418-22
– reference: 9430591 - Science. 1998 Jan 16;279(5349):393-6
– reference: 21760928 - PLoS One. 2011;6(7):e21942
– reference: 19712040 - J Infect Dis. 2009 Oct 1;200(7):1113-8
– reference: 19234466 - Nat Struct Mol Biol. 2009 Mar;16(3):265-73
– reference: 18694338 - J Infect Dis. 2008 Sep 1;198(5):635-41
– reference: 10657821 - J Pediatr. 2000 Feb;136(2):168-75
– reference: 18237269 - J Infect Dis. 2008 Feb 15;197(4):580-3
– reference: 19251591 - Science. 2009 Apr 10;324(5924):246-51
– reference: 23369412 - Lancet Infect Dis. 2013 Mar;13(3):238-50
– reference: 12639491 - Vaccine. 2003 Apr 2;21(15):1687-93
– reference: 19931380 - Vaccine. 2010 Apr 9;28(17):3025-9
– reference: 20389023 - J Clin Invest. 2010 May;120(5):1663-73
– reference: 23726847 - Virus Res. 2013 Dec 5;178(1):78-98
– reference: 11166898 - Vaccine. 2001 Feb 8;19(13-14):1732-7
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Snippet Background. Highly pathogenic avian influenza A(H5N1) causes severe infections in humans. We generated 2 influenza A(H5N1) live attenuated influenza vaccines...
Highly pathogenic avian influenza A(H5N1) causes severe infections in humans. We generated 2 influenza A(H5N1) live attenuated influenza vaccines for pandemic...
Background.  Highly pathogenic avian influenza A(H5N1) causes severe infections in humans. We generated 2 influenza A(H5N1) live attenuated influenza vaccines...
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Aggregation Database
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Enrichment Source
Publisher
StartPage 1860
SubjectTerms Adult
Antibodies
Antibodies, Viral - blood
Antibody Affinity
Antibody Formation - immunology
Antibody response
Applied microbiology
Attenuated vaccines
Biological and medical sciences
Cross Reactions
Dosage
Female
Fundamental and applied biological sciences. Psychology
H5N1 subtype influenza A virus
Healthy Volunteers
Hemagglutination Inhibition Tests
Humans
Inactivated vaccines
Infectious diseases
Influenza A virus
Influenza A Virus, H5N1 Subtype - immunology
Influenza A Virus, H7N3 Subtype - immunology
Influenza vaccines
Influenza Vaccines - immunology
Influenza Vaccines - therapeutic use
Major and Brief Reports
Male
Medical sciences
Microbiology
Middle Aged
Miscellaneous
Pandemics
Transcriptional regulatory elements
Vaccines, antisera, therapeutical immunoglobulins and monoclonal antibodies (general aspects)
Vaccines, Attenuated - immunology
Vaccines, Attenuated - therapeutic use
Virology
VIRUSES
Young Adult
Title A Live Attenuated Influenza A(H5N1) Vaccine Induces Long-Term Immunity in the Absence of a Primary Antibody Response
URI https://www.jstor.org/stable/43707574
https://www.ncbi.nlm.nih.gov/pubmed/24604819
https://www.proquest.com/docview/1530955621
https://www.proquest.com/docview/1618159432
https://pubmed.ncbi.nlm.nih.gov/PMC4047295
Volume 209
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