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In this study, we investigated the adjuvant activity of CIA06, an adjuvant system that is composed of a toll-like receptor 4 agonist de-<jats:italic>O<\/jats:italic>-acylated lipooligosaccharide (dLOS) and aluminum hydroxide, on the H1N1 pandemic influenza vaccine Greenflu-S\u00ae in mice. CIA06 significantly enhanced influenza-specific serum IgG, hemagglutination-inhibition, and virus-neutralizing antibody titers, which eliminated vaccine dose-dependency in the antibody response. Mice immunized with the CIA06-adjuvanted Greenflu-S showed Th1-type-predominant cytokine profiles, and both CD4<jats:sup>+<\/jats:sup>and CD8<jats:sup>+<\/jats:sup>T cell responses were induced. Immunization of mice with the CIA06-adjuvanted vaccine reduced the mortality and morbidity of mice upon lethal challenges with influenza virus, and no excessive inflammatory responses were observed in the lung tissues of the immunized mice after viral infection. These data suggest that the dLOS-based adjuvant system CIA06 can be used to promote the immune responses to influenza vaccine or to spare antigen dose without causing harmful inflammatory responses.<\/jats:p>","DOI":"10.1155\/2016\/3713656","type":"journal-article","created":{"date-parts":[[2016,11,7]],"date-time":"2016-11-07T21:07:32Z","timestamp":1478552852000},"page":"1-12","source":"Crossref","is-referenced-by-count":8,"title":["A De-<i>O<\/i>-acylated Lipooligosaccharide-Based Adjuvant System Promotes Antibody and Th1-Type Immune Responses to H1N1 Pandemic Influenza Vaccine in Mice"],"prefix":"10.1155","volume":"2016","author":[{"given":"Ji In","family":"Ryu","sequence":"first","affiliation":[{"name":"Department of Bioscience and Biotechnology, Sejong University, Seoul, Republic of Korea"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Shin Ae","family":"Park","sequence":"additional","affiliation":[{"name":"Department of Bioscience and Biotechnology, Sejong 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