tetano
Editor, Senior Moderator
NPJ Vaccines. 2019 May 29;4:22. doi: 10.1038/s41541-019-0114-8. eCollection 2019.
[h=1]Heterologous prime-boost with A(H5N1) pandemic influenza vaccines induces broader cross-clade antibody responses than homologous prime-boost.[/h] Levine MZ[SUP]1[/SUP], Holiday C[SUP]1[/SUP], Jefferson S[SUP]1[/SUP], Gross FL[SUP]1,[/SUP][SUP]2[/SUP], Liu F[SUP]1[/SUP], Li S[SUP]3,[/SUP][SUP]4[/SUP], Friel D[SUP]5[/SUP], Boutet P[SUP]5[/SUP], Innis BL[SUP]6,[/SUP][SUP]7[/SUP], Mallett CP[SUP]6[/SUP], Tumpey TM[SUP]1[/SUP], Stevens J[SUP]1[/SUP], Katz JM[SUP]1[/SUP].
[h=3]Author information[/h]
[h=3]Abstract[/h] Highly pathogenic avian influenza (HPAI) A(H5Nx) viruses continue to pose a pandemic threat. US national vaccine stockpiles are a cornerstone of the influenza pandemic preparedness plans. However, continual genetic and antigenic divergence of A(H5Nx) viruses requires the development of effective vaccination strategies using stockpiled vaccines and adjuvants for pandemic preparedness. Human sera collected from healthy adults who received either homologous (2 doses of a AS03[SUB]A[/SUB]-adjuvanted A/turkey/Turkey/1/2005, A/Turkey), or heterologous (primed with AS03[SUB]A[/SUB]-adjuvanted A/Indonesia/5/2005, A/Indo, followed by A/Turkey boost) prime-boost vaccination regimens were analyzed by hemagglutination inhibition and microneutralization assays against 8 wild-type HPAI A(H5Nx) viruses from 6 genetic clades. Molecular, structural and antigenic features of the A(H5Nx) viruses that could influence the cross-clade antibody responses were also explored. Compared with homologous prime-boost vaccinations, priming with a clade 2.1.3.2 antigen (A/Indo) followed by one booster dose of a clade 2.2.1 antigen (A/Turkey) administered 18 months apart did not compromise the antibody responses to the booster vaccine (A/Turkey), it also broadened the cross-clade antibody responses to several antigenically drifted variants from 6 heterologous clades, including an antigenically distant A(H5N8) virus (A/gyrfalcon/Washington/410886/2014, clade 2.3.4.4) that caused recent outbreaks in US poultry. The magnitude and breadth of the cross-clade antibody responses against emerging HPAI A(H5Nx) viruses are associated with genetic, structural and antigenic differences from the vaccine viruses and enhanced by the inclusion of an adjuvant. Heterologous prime-boost vaccination with AS03[SUB]A[/SUB] adjuvanted vaccine offers a vaccination strategy to use existing stockpiled vaccines for pandemic preparedness against new emerging HPAI A(H5Nx) viruses.
[h=4]KEYWORDS:[/h] Diseases; Immunology; Influenza virus; Medical research
PMID: 31149353 PMCID: PMC6541649 DOI: 10.1038/s41541-019-0114-8
[h=1]Heterologous prime-boost with A(H5N1) pandemic influenza vaccines induces broader cross-clade antibody responses than homologous prime-boost.[/h] Levine MZ[SUP]1[/SUP], Holiday C[SUP]1[/SUP], Jefferson S[SUP]1[/SUP], Gross FL[SUP]1,[/SUP][SUP]2[/SUP], Liu F[SUP]1[/SUP], Li S[SUP]3,[/SUP][SUP]4[/SUP], Friel D[SUP]5[/SUP], Boutet P[SUP]5[/SUP], Innis BL[SUP]6,[/SUP][SUP]7[/SUP], Mallett CP[SUP]6[/SUP], Tumpey TM[SUP]1[/SUP], Stevens J[SUP]1[/SUP], Katz JM[SUP]1[/SUP].
[h=3]Author information[/h]
[h=3]Abstract[/h] Highly pathogenic avian influenza (HPAI) A(H5Nx) viruses continue to pose a pandemic threat. US national vaccine stockpiles are a cornerstone of the influenza pandemic preparedness plans. However, continual genetic and antigenic divergence of A(H5Nx) viruses requires the development of effective vaccination strategies using stockpiled vaccines and adjuvants for pandemic preparedness. Human sera collected from healthy adults who received either homologous (2 doses of a AS03[SUB]A[/SUB]-adjuvanted A/turkey/Turkey/1/2005, A/Turkey), or heterologous (primed with AS03[SUB]A[/SUB]-adjuvanted A/Indonesia/5/2005, A/Indo, followed by A/Turkey boost) prime-boost vaccination regimens were analyzed by hemagglutination inhibition and microneutralization assays against 8 wild-type HPAI A(H5Nx) viruses from 6 genetic clades. Molecular, structural and antigenic features of the A(H5Nx) viruses that could influence the cross-clade antibody responses were also explored. Compared with homologous prime-boost vaccinations, priming with a clade 2.1.3.2 antigen (A/Indo) followed by one booster dose of a clade 2.2.1 antigen (A/Turkey) administered 18 months apart did not compromise the antibody responses to the booster vaccine (A/Turkey), it also broadened the cross-clade antibody responses to several antigenically drifted variants from 6 heterologous clades, including an antigenically distant A(H5N8) virus (A/gyrfalcon/Washington/410886/2014, clade 2.3.4.4) that caused recent outbreaks in US poultry. The magnitude and breadth of the cross-clade antibody responses against emerging HPAI A(H5Nx) viruses are associated with genetic, structural and antigenic differences from the vaccine viruses and enhanced by the inclusion of an adjuvant. Heterologous prime-boost vaccination with AS03[SUB]A[/SUB] adjuvanted vaccine offers a vaccination strategy to use existing stockpiled vaccines for pandemic preparedness against new emerging HPAI A(H5Nx) viruses.
[h=4]KEYWORDS:[/h] Diseases; Immunology; Influenza virus; Medical research
PMID: 31149353 PMCID: PMC6541649 DOI: 10.1038/s41541-019-0114-8