Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10965274 | Vaccine | 2014 | 9 Pages |
Abstract
The commonly used inactivated or split influenza vaccines induce only induce minimal T cell responses and are less effective in preventing heterologous virus infection. Thus, developing cross-protective influenza vaccines against the spread of a new influenza virus is an important strategy against pandemic emergence. Here we demonstrated that immunization with heat shock protein gp96 as adjuvant led to a dramatic increased antigen-specific T cell response to a pandemic H1N1 split vaccine. Notably, gp96 elicited a cross-protective CD8+ T cell response to the internal conserved viral protein NP. Although the split pH1N1vaccine alone has low cross-protective efficiency, adding gp96 as an adjuvant effectively improved the cross-protection against challenge with a heterologous virus in mice. Our study reveals the novel property of gp96 in boosting the T cell response against conserved epitopes of influenza virus and its potential use as an adjuvant for human pre-pandemic inactivated influenza vaccines against different viral subtypes.
Keywords
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Immunology
Authors
Ying Ju, Hongxia Fan, Jun Liu, Jun Hu, Xinghui Li, Changfei Li, Lizhao Chen, Qiang Gao, George F. Gao, Songdong Meng,