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2014 Fiscal Year Final Research Report

Analysis of viral infection and innate immune response using humanized mice

Research Project

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Project/Area Number 24390112
Research Category

Grant-in-Aid for Scientific Research (B)

Allocation TypePartial Multi-year Fund
Section一般
Research Field Virology
Research InstitutionKyoto University

Principal Investigator

KOYANAGI Yoshio  京都大学, ウイルス研究所, 教授 (80215417)

Project Period (FY) 2012-04-01 – 2015-03-31
Keywordsヒト化マウス / ウイルス制御因子 / HIV / tetherin / APOBEC3
Outline of Final Research Achievements

Using a human hematopoietic stem cell-transplanted humanized mouse model, we found a series of HIV-1 infection mechanisms. Vpu contributes to efficient spread of HIV-1 in vivo. Vpu concomitantly downregulates tetherin and CD4 from the surface of infected cells. Vpr induces depletion of CCR5+ FOXP3+ CD4+ regulatory T cells (Treg) for enhancing viremia of CCR5-tropic HIV-1. APOBEC3F and APOBEC3G fundamentally work as restriction factors against HIV-1 in vivo, but at the same time, that APOBEC3F are capable of promoting viral diversification and evolution in vivo.

Free Research Field

ウイルス学

URL: 

Published: 2016-06-03  

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