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Development of new treatment strategies for HIV -1 infection

Research Project

Project/Area Number 24591486
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Research Field Infectious disease medicine
Research InstitutionShowa Pharmaceutical University

Principal Investigator

HAMADA Koichi  昭和薬科大学, 薬学部, 助教 (00343070)

Project Period (FY) 2012-04-01 – 2015-03-31
Project Status Completed (Fiscal Year 2014)
Budget Amount *help
¥5,460,000 (Direct Cost: ¥4,200,000、Indirect Cost: ¥1,260,000)
Fiscal Year 2014: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Fiscal Year 2013: ¥1,950,000 (Direct Cost: ¥1,500,000、Indirect Cost: ¥450,000)
Fiscal Year 2012: ¥1,950,000 (Direct Cost: ¥1,500,000、Indirect Cost: ¥450,000)
KeywordsHIV-1 / 潜伏感染 / PI3K/PTEN / HIV
Outline of Final Research Achievements

The presence of latent vial infection has prevented the eradication of human immunodeficiency virus (HIV) from infected patients successfully treated with anti-retroviral therapy. Combination antiretroviral therapy (cART) can effectively suppress HIV-1 replication, but the latent viral reservoir is impervious to cART and represents a major barrier to curing HIV-1 infection.
PI3K/PTEN/GSK-3β pathway is a critical role for cell proliferation and survival. In this study, we identified that PI3K/PTEN/GSK-3β pathway is necessary to HIV infection and reactivation.

Report

(4 results)
  • 2014 Annual Research Report   Final Research Report ( PDF )
  • 2013 Research-status Report
  • 2012 Research-status Report
  • Research Products

    (1 results)

All 2012

All Presentation (1 results)

  • [Presentation] Critical Role of the PI3K/PTEN/GSK-3 Signaling Pathway in HIV latent infected cells2012

    • Author(s)
      濱田浩一、水谷顕洋、岡田誠治
    • Organizer
      第85回日本生化学会大会
    • Place of Presentation
      福岡国際会議場、マリンメッセ福岡(福岡市)
    • Related Report
      2012 Research-status Report

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Published: 2013-05-31   Modified: 2019-07-29  

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