Positive Contribution of Adjuvanted Influenza Vaccines to the Resolution of Bacterial Superinfections. (9th February 2016)

• Record Type: Journal Article
• Authors: Zurli, Vanessa; Gallotta, Marilena; Taccone, Marianna; Chiarot, Emiliano; Brazzoli, Michela; Corrente, Federica; Bonci, Alessandra; Casini, Daniele; De Gregorio, Ennio; Baudner, Barbara C.; Bertholet, Sylvie; Seubert, Anja
• Is Part Of: Journal of infectious diseases. Volume 213:Number 12(2016:Jun. 15)
• Page Start: 1876
• Page End: 1885
• Publication Date: 2016-02-09
• Subjects: influenza -- bacterial superinfection -- vaccine adjuvants -- Staphylococcus aureus -- MF59 -- CpG -- LTK63; Communicable diseases -- Periodicals; Diseases -- Causes and theories of causation -- Periodicals; Medicine -- Periodicals; Communicable Diseases -- Periodicals; Electronic journals; 616.9
• DOI: 10.1093/infdis/jiw048
• Languages: English
• ISSNs: 0022-1899

Abstract

Abstract: Background. Most preclinical studies assess vaccine effectiveness in single-pathogen infection models. This is unrealistic given that humans are continuously exposed to different commensals and pathogens in sequential and mixed infections. Accordingly, complications from secondary bacterial infection are a leading cause of influenza-associated morbidity and mortality. New vaccination strategies are needed to control infections on simultaneous fronts. Methods. We compared different anti-influenza vaccines for their protective potential in a model of viral infection with bacterial superinfection. Mice were immunized with H1N1/A/California/7/2009 subunit vaccines, formulated with different adjuvants inducing either T-helper type 1 (Th1) (MF59 plus CpG)–, Th1/2 (MF59)–, or Th17 (LTK63)–prone immune responses and were sequentially challenged with mouse-adapted influenza virus H1N1/A/Puerto Rico/8/1934 and Staphylococcus aureus USA300, a clonotype emerging as a leading contributor in postinfluenza pneumonia in humans. Results. Unadjuvanted vaccine controlled single viral infection, yet mice had considerable morbidity from viral disease and bacterial superinfection. In contrast, all adjuvanted vaccines efficiently protected mice in both conditions. Interestingly, the Th1-inducing formulation was superior to Th1/2 or Th17 inducers. Conclusions. Our studies should help us better understand how differential immunity to influenza skews immune responses toward coinfecting bacteria and discover novel modes to prevent bacterial superinfections in the lungs of persons with influenza.