scholarly journals Clinical and Immune Responses to Inactivated Influenza A(H1N1)pdm09 Vaccine in Children

2014 ◽  
Vol 33 (8) ◽  
pp. 865-871 ◽  
Author(s):  
Karen L. Kotloff ◽  
Natasha B. Halasa ◽  
Christopher J. Harrison ◽  
Janet A. Englund ◽  
Emmanuel B. Walter ◽  
...  
Vaccines ◽  
2019 ◽  
Vol 7 (3) ◽  
pp. 64 ◽  
Author(s):  
Jorma Hinkula ◽  
Sanna Nyström ◽  
Claudia Devito ◽  
Andreas Bråve ◽  
Steven E. Applequist

Background: Vaccination is commonly used to prevent and control influenza infection in humans. However, improvements in the ease of delivery and strength of immunogenicity could markedly improve herd immunity. The aim of this pre-clinical study is to test the potential improvements to existing intranasal delivery of formalin-inactivated whole Influenza A vaccines (WIV) by formulation with a cationic lipid-based adjuvant (N3). Additionally, we combined WIV and N3 with a DNA-encoded TLR5 agonist secreted flagellin (pFliC(-gly)) as an adjuvant, as this adjuvant has previously been shown to improve the effectiveness of plasmid-encoded DNA antigens. Methods: Outbred and inbred mouse strains were intranasally immunized with unadjuvanted WIV A/H1N1/SI 2006 or WIV that was formulated with N3 alone. Additional groups were immunized with WIV and N3 adjuvant combined with pFliC(-gly). Homo and heterotypic humoral anti-WIV immune responses were assayed from serum and lung by ELISA and hemagglutination inhibition assay. Homo and heterotypic cellular immune responses to WIV and Influenza A NP were also determined. Results: WIV combined with N3 lipid adjuvant the pFliC(-gly) significantly increased homotypic influenza specific serum antibody responses (>200-fold), increased the IgG2 responses, indicating a mixed Th1/Th2-type immunity, and increased the HAI-titer (>100-fold). Enhanced cell-mediated IFNγ secreting influenza directed CD4+ and CD8+ T cell responses (>40-fold) to homotypic and heterosubtypic influenza A virus and peptides. Long-term and protective immunity was obtained. Conclusions: These results indicate that inactivated influenza virus that was formulated with N3 cationic adjuvant significantly enhanced broad systemic and mucosal influenza specific immune responses. These responses were broadened and further increased by incorporating DNA plasmids encoding FliC from S. typhimurum as an adjuvant providing long lasting protection against heterologous Influenza A/H1N1/CA09pdm virus challenge.


2014 ◽  
Vol 14 (1) ◽  
Author(s):  
Jin Lv ◽  
Dan Wang ◽  
Yan-Hong Hua ◽  
Shi-Jia Pei ◽  
Jin Wang ◽  
...  

2011 ◽  
Vol 204 (1) ◽  
pp. S249
Author(s):  
Barbra M. Fisher ◽  
Janice Scott ◽  
Jan Hart ◽  
Anne Lynch ◽  
Virginia D. Winn ◽  
...  

Vaccines ◽  
2020 ◽  
Vol 8 (1) ◽  
pp. 123 ◽  
Author(s):  
Xinyu Zhuang ◽  
Yanxin Qi ◽  
Maopeng Wang ◽  
Ning Yu ◽  
Fulong Nan ◽  
...  

The design of the mRNA vaccine involves the selection of in vitro transcription (IVT) systems and nonviral delivery vectors. This study aimed to verify the effect of 5’ and 3’ untranslated region (UTR) sequences on the translation efficiency of mRNA. Three modes of IVT-mRNA systems (IVT-mRNA-n1/n2/n3) with diverse UTRs were constructed, and EGFP (enhanced green fluorescent protein) and HA (hemagglutinin) gene of H3N2 influenza virus were introduced into each of them. The results showed that the mode of 5’ and 3’ UTRs originating from human β-globulin was better than the mode of UTRs from human α-globulin, and the n3 mode was the best. mEGFP-n3, mH3HA-n3, and mLuciferease-n3 were prepared to compare the effect of cationic lipid nanoparticle (LNP) with that of mannose-conjugated LNP (LNP-Man) on the efficiency of gene delivery. The results showed that the effect of LNP-Man was better than that of LNP both in vitro and in vivo. Choosing appropriate ligands might help in vaccine design. After selecting the IVT-mRNA-n3 system and delivery vectors, mRNA vaccines were constructed against the H1N1 influenza virus, and C57BL/6 mice were immunized through intranasal administration. The results showed that mRNA vaccines could elicit both humoral and cellular immune responses and completely protect mice from the tenfold LD50 H1N1 influenza virus challenge.


Vaccine ◽  
2014 ◽  
Vol 32 (7) ◽  
pp. 881-887 ◽  
Author(s):  
Inna G. Ovsyannikova ◽  
Sarah J. White ◽  
Beth R. Larrabee ◽  
Diane E. Grill ◽  
Robert M. Jacobson ◽  
...  

2013 ◽  
Vol 158 (11) ◽  
pp. 2267-2272 ◽  
Author(s):  
Yu Huang ◽  
Wei Zhu ◽  
Xing Zeng ◽  
Shasha Li ◽  
Xiaoyan Li ◽  
...  

PLoS ONE ◽  
2011 ◽  
Vol 6 (12) ◽  
pp. e28627 ◽  
Author(s):  
Aliyah Baluch ◽  
Atul Humar ◽  
Adrian Egli ◽  
Jonathan Gubbay ◽  
Luiz Lisboa ◽  
...  

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