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Sex bias in mouse humoral immune response to influenza vaccine depends on the vaccine type

tetano

Editor, Senior Moderator
Biologicals. 2018 Feb 6. pii: S1045-1056(18)30023-X. doi: 10.1016/j.biologicals.2018.01.007. [Epub ahead of print]
[h=1]Sex bias in mouse humoral immune response to influenza vaccine depends on the vaccine type.[/h] ?ivković I[SUP]1[/SUP], Petrović R[SUP]1[/SUP], Arsenović-Ranin N[SUP]2[/SUP], Petru?ić V[SUP]1[/SUP], Minić R[SUP]1[/SUP], Bufan B[SUP]2[/SUP], Popović O[SUP]1[/SUP], Leposavić G[SUP]3[/SUP].
[h=3]Author information[/h]

[h=3]Abstract[/h] The study explored influence of biological sex on development of humoral immune response to seasonal trivalent whole inactivated virus (WIV) and split virus (SV) influenza vaccines in outbred Swiss mouse model. To this end, mice of both sexes were immunized with WIV (WIV mice) and SV vaccines (SV mice) and examined for specific antibody response. Irrespective of sex, total IgG and neutralizing antibody responses to distinct virus strains were weaker in SV than in WIV mice. In WIV mice of both sexes, irrespective of strain specificity, IgG isotype response was dominated by IgG2a antibodies, while in SV mice nearly equal representation of IgG2a and IgG1 antibodies was found. The analyses of sex differences showed higher titers of H1N1-specific and both H1N1- and H3N2-specific total IgG and neutralizing antibodies in female WIV and SV mice, respectively. Additionally, sexual dimorphism in IgG subclass profile depended on vaccine type. Specifically, compared with males, in females WIV shifted IgG2a/IgG1 antibody ratio towards IgG2a isotype on the account of weaker IgG1 response, whereas in SV mice, irrespective of virus strain, IgG2a and IgG1 isotypes were equally represented in both sexes. These findings indicate the vaccine type-dependent sex bias in antibody response to inactivated influenza vaccines.


[h=4]KEYWORDS:[/h] Antibody response; Influenza virus strain; Sex differences; Split virus influenza vaccine; Whole virus influenza vaccine

PMID: 29426673 DOI: 10.1016/j.biologicals.2018.01.007
 
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