• Search Research Projects
  • Search Researchers
  • How to Use
  1. Back to project page

2014 Fiscal Year Final Research Report

Perturbed immune system by HTLV-1

Planned Research

  • PDF
Project AreaConversion of tumor-regulation vector to intercept oncogenic spiral accelerated by infection and inflammation
Project/Area Number 22114003
Research Category

Grant-in-Aid for Scientific Research on Innovative Areas (Research in a proposed research area)

Allocation TypeSingle-year Grants
Review Section Biological Sciences
Research InstitutionKyoto University

Principal Investigator

MATSUOKA Masao  京都大学, ウイルス研究所, 教授 (10244138)

Project Period (FY) 2010-04-01 – 2015-03-31
KeywordsHTLV-1 / HBZ / Foxp3 / Tax / 炎症 / ウイルス発がん
Outline of Final Research Achievements

HTLV-1 bZIP factor (HBZ) gene is encoded in the minus strand of HTLV-1 provirus. The HBZ gene is constantly expressed in ATL cells and HTLV-1 infected cells. HBZ enhances transcription of Foxp3 gene through activation of TGF-β pathway. However, since this expression is unstable, Foxp3+ T cells are converted to Foxp3- T cells, which highly produce IFN-γ. Overproduction of IFN-γ is associated with inflammation and lymphomagenesis. Transcription factors, TCF1 and LEF1, inhibit function of Tax. Therefore, HTLV-1 infected cells are rare in thymic T cells that highly express TCF1 and LEF1. This is the mechanism why HTLV-1 favors effector/memory T cells in vivo.

Free Research Field

ウイルス学

URL: 

Published: 2016-06-03  

Information User Guide FAQ News Terms of Use Attribution of KAKENHI

Powered by NII kakenhi