scholarly journals Inclusion of Flagellin during Vaccination against Influenza Enhances Recall Responses in Nonhuman Primate Neonates

2015 ◽  
Vol 89 (14) ◽  
pp. 7291-7303 ◽  
Author(s):  
Jong R. Kim ◽  
Beth C. Holbrook ◽  
Sarah L. Hayward ◽  
Lance K. Blevins ◽  
Matthew J. Jorgensen ◽  
...  

ABSTRACTInfluenza virus can cause life-threatening infections in neonates and young infants. Although vaccination is a major countermeasure against influenza, current vaccines are not approved for use in infants less than 6 months of age, in part due to the weak immune response following vaccination. Thus, there is a strong need to develop new vaccines with improved efficacy for this vulnerable population. To address this issue, we established a neonatal African green monkey (AGM) nonhuman primate model that could be used to identify effective influenza vaccine approaches for use in young infants. We assessed the ability of flagellin, a Toll-like receptor 5 (TLR5) agonist, to serve as an effective adjuvant in this at-risk population. Four- to 6-day-old AGMs were primed and boosted with inactivated PR8 influenza virus (IPR8) adjuvanted with either wild-type flagellin or inactive flagellin with a mutation at position 229 (m229), the latter of which is incapable of signaling through TLR5. Increased IgG responses were observed following a boost, as well as at early times after challenge, in infants vaccinated with flagellin-adjuvanted IPR8. Inclusion of flagellin during vaccination also resulted in a significantly increased number of influenza virus-specific T cells following challenge compared to the number in infants vaccinated with the m229 adjuvant. Finally, following challenge infants vaccinated with IPR8 plus flagellin exhibited a reduced pathology in the lungs compared to that in infants that received IPR8 plus m229. This study provides the first evidence of flagellin-mediated enhancement of vaccine responses in nonhuman primate neonates.IMPORTANCEYoung infants are particularly susceptible to severe disease as a result of influenza virus infection. Compounding this is the lack of effective vaccines for use in this vulnerable population. Here we describe a vaccine approach that results in improved immune responses and protection in young infants. Incorporation of flagellin during vaccination resulted in increased antibody and T cell responses together with reduced disease following virus infection. These results suggest that flagellin may serve as an effective adjuvant for vaccines targeted to this vulnerable population.

Virology ◽  
2015 ◽  
Vol 476 ◽  
pp. 124-133 ◽  
Author(s):  
Beth C. Holbrook ◽  
Sarah L. Hayward ◽  
Lance K. Blevins ◽  
Nancy Kock ◽  
Tyler Aycock ◽  
...  

2011 ◽  
Vol 165 (2) ◽  
pp. 104 ◽  
Author(s):  
Angelia A. Eick ◽  
Timothy M. Uyeki ◽  
Alexander Klimov ◽  
Henrietta Hall ◽  
Raymond Reid ◽  
...  

2011 ◽  
Vol 66 (6) ◽  
pp. 333-334
Author(s):  
Angelia A. Eick ◽  
Timothy M. Uyeki ◽  
Alexander Klimov ◽  
Henrietta Hall ◽  
Raymond Reid ◽  
...  

2015 ◽  
Vol 83 (10) ◽  
pp. 3764-3770 ◽  
Author(s):  
Agnieszka Rynda-Apple ◽  
Keven M. Robinson ◽  
John F. Alcorn

Seasonal influenza virus infection presents a major strain on the health care system. Influenza virus infection has pandemic potential, which was repeatedly observed during the last century. Severe disease may occur in the young, in the elderly, in those with preexisting lung disease, and in previously healthy individuals. A common cause of severe influenza pathogenesis is superinfection with bacterial pathogens, namely,Staphylococcus aureusandStreptococcus pneumoniae. A great deal of recent research has focused on the immune pathways involved in influenza-induced susceptibility to secondary bacterial pneumonia. Both innate and adaptive antibacterial host defenses are impaired in the context of preceding influenza virus infection. The goal of this minireview is to highlight these findings and synthesize these data into a shared central theme of pathogenesis.


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