Analysis of immune escape mechanism of novel HIV-2 variants isolated from AIDS patients
Project/Area Number |
26860777
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Research Category |
Grant-in-Aid for Young Scientists (B)
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Allocation Type | Multi-year Fund |
Research Field |
Infectious disease medicine
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Research Institution | Okayama University (2015) National Hospital Organization Nagoya Medical Center (2014) |
Principal Investigator |
Nemoto Michiko 岡山大学, その他の研究科, 助教 (30625926)
|
Project Period (FY) |
2014-04-01 – 2016-03-31
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Project Status |
Completed (Fiscal Year 2015)
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Budget Amount *help |
¥3,770,000 (Direct Cost: ¥2,900,000、Indirect Cost: ¥870,000)
Fiscal Year 2015: ¥1,300,000 (Direct Cost: ¥1,000,000、Indirect Cost: ¥300,000)
Fiscal Year 2014: ¥2,470,000 (Direct Cost: ¥1,900,000、Indirect Cost: ¥570,000)
|
Keywords | HIV-2 / 組換え流行株 / 宿主因子 / 293T細胞 / HeLa細胞 / 細胞指向性 / HIV感染抑制因子 / 初代培養細胞 |
Outline of Final Research Achievements |
In vitro replication kinetics of novel HIV-2 circulating recombinant forms in various cell lines as well as in primary cells have been studied. The chemokine receptor CCR5 is used by novel HIV-2 circulating recombinant forms as a coreceptor to enter cells. The findings from this study not only offer academic knowledge of novel HIV-2 circulating recombinant forms, but also help improve treatment for these novel HIV-2 infected patients.
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Report
(3 results)
Research Products
(4 results)
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[Journal Article] Structural Insights into HIV-1 Vif-APOBEC3F Interaction2016
Author(s)
Nakashima M, Ode H, Kawamura T, Kitamura S, Naganawa Y, Awazu H, Tsuzuki S, Matsuoka K, Nemoto M, Hachiya A, Sugiura W, Yokomaku Y, Watanabe N, Iwatani Y
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Journal Title
Journal of Virology
Volume: 90
Issue: 2
Pages: 1034-1047
DOI
Related Report
Peer Reviewed / Acknowledgement Compliant
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