Back to Search Start Over

Distinct patterns of cellular immune response elicited by influenza non-adjuvanted and AS03-adjuvanted monovalent H1N1(pdm09) vaccine.

Authors :
Giarola-Silva S
Coelho-Dos-Reis JGA
Mourão MM
Campi-Azevedo AC
Nakagaki Silva EE
Luiza-Silva M
Martins MA
Silveira-Cassette ACO
Batista MA
Peruhype-Magalhães V
Antonelli LRDV
Leite Ribeiro JG
Elói-Santos SM
Machado AV
Teixeira-Carvalho A
Martins-Filho OA
Araújo MSS
Source :
Antiviral research [Antiviral Res] 2017 Aug; Vol. 144, pp. 70-82. Date of Electronic Publication: 2017 May 23.
Publication Year :
2017

Abstract

The study aimed at identifying biomarkers of immune response elicited by non-adjuvanted-(NAV) and adjuvanted-(AV) H1N1(pdm09) vaccines. The results showed that despite both vaccines elicited similar levels of anti-H1N1 antibodies at day30 after vaccination, higher reactivity was observed in AV at day180. While AV induced early changes in cell-surface molecules on monocytes, CD4 <superscript>+</superscript> , CD8 <superscript>+</superscript> T-cells and B-cells, NAV triggered minor changes, starting later on at day3. Furthermore, AV induced a late and persistent increase in TLR gene expression after day3, except for tlr4, while NAV displayed earlier but transient tlr3/4/7/9 up-regulation. Contrasting with NAV, prominent chemokine gene expression (cxcl8,cxcl9,ccl5) and a broad spectrum up-regulation of plasmatic biomarkers (CXCL8,IL-6,IL-1β,IL-12,IL-10) was evident in AV, which showed a major involvement of TNF and IL-10. Similarly, AV induced a robust IL-10-modulated proinflammatory storm, with early and persistent involvement of TNF-α/IL-12/IFN-γ axis derived from NK-cells, CD4 <superscript>+</superscript> and CD8 <superscript>+</superscript> T-cells along with promiscuous production of IL-4/IL-5/IL-13. Conversely, NAV promotes a concise and restricted intracytoplasmic chemokine/cytokine response, essentially mediated by TNF-α and IL-4, with late IL-10 production by CD8 <superscript>+</superscript> T-cells. Systems biology approach underscored that AV guided the formation of an imbricate network characterized by a progressive increase in the number of neighborhood connections amongst innate and adaptive immunity. In AV, the early cross-talk between innate and adaptive immunity, followed by the triad NK/CD4 <superscript>+</superscript> /CD8 <superscript>+</superscript> T-cells at day3, sponsored a later/robust biomarker network. These findings indicate the relevance of adjuvanted vaccination to orchestrate broad, balanced and multifactorial cellular immune events that lead ultimately to a stronger H1N1 humoral immunity.<br /> (Copyright © 2017 Elsevier B.V. All rights reserved.)

Details

Language :
English
ISSN :
1872-9096
Volume :
144
Database :
MEDLINE
Journal :
Antiviral research
Publication Type :
Academic Journal
Accession number :
28549970
Full Text :
https://doi.org/10.1016/j.antiviral.2017.05.009