The novel adjuvant IC31^® strongly improves influenza vaccine-specific cellular and humoral immune responses in young adult and aged mice

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• 作者：Karin Riedl ; Rosemarie Riedl ; Alex ; er von Gabain ; Eszter Nagy ; Karen Lingnau
• 关键词：Influenza ; IC31^® ; ; Type 1 immune responses ; Aged mice
• 刊名：Vaccine
• 出版年：2008
• 期刊代码：89_0264410x
• 类别：imm
• 出版时间：25 June 2008
• 卷：26
• 期：27-28
• 页码：3461-3468
• 文件大小：392 K

摘要

The compromised immune responses in the elderly as well as the threat of pandemic influenza necessitate the development of improved influenza vaccines. This study provides evidence that IC31^®, a two-component synthetic adjuvant signalling through TLR-9, augments humoral and cellular immune responses to seasonal influenza vaccines. Experiments performed in young adult mice showed increased HI titres and higher levels of IgG2a antibodies that were accompanied by the induction of IFN-γ producing CD4⁺ T cells after single vaccination with reduced doses of vaccine antigens, even 200 days after single immunisation. Importantly, similar effects were seen in aged mice, although most pronounced upon booster immunisation. Thus, IC31^® fulfils important criteria of novel influenza vaccine adjuvants.