2017 Fiscal Year Final Research Report
Cross-protective antibody responses against influenza virus infection
Project/Area Number |
16K19167
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Research Category |
Grant-in-Aid for Young Scientists (B)
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Allocation Type | Multi-year Fund |
Research Field |
Immunology
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Research Institution | National Institute of Infectious Diseases |
Principal Investigator |
Adachi Yu 国立感染症研究所, 免疫部, 主任研究官 (40749016)
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Project Period (FY) |
2016-04-01 – 2018-03-31
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Keywords | インフルエンザ / B細胞 / 交差防御抗体 / インフルエンザワクチン / 免疫学 |
Outline of Final Research Achievements |
We previously found that cross-reactive B cells were highly selected in lung germinal centers (GCs) following influenza virus infection. In this study, we identified that an occluded epitope in hemagglutinin (HA) stem region for lung cross-reactive GC B cells. This epitope is occluded in native trimeric HA structure, but is exposed in post-fusion HA structure to occur under low-pH during viral replication. Furthermore, immunization by post-fusion HA antigen induces a class of protective antibody which have broad specificity.
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Free Research Field |
免疫学
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Academic Significance and Societal Importance of the Research Achievements |
本研究で見出した交差防御抗体は、ヒト記憶B細胞にも存在することからユニバーサルワクチンの新たな標的抗体になると考えられる。さらに、この交差防御抗体を選択可能な構造改変型ワクチン剤形は、現行ワクチンから簡便に作製可能であり、新規ユニバーサルワクチン剤形となることが期待される。
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