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2017 Fiscal Year Final Research Report

Mechanism of induction of high-functional HIV-1-specific CD8 T cells from naive T cells

Research Project

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Project/Area Number 16K19159
Research Category

Grant-in-Aid for Young Scientists (B)

Allocation TypeMulti-year Fund
Research Field Immunology
Research InstitutionKumamoto University

Principal Investigator

KUSE NOZOMI  熊本大学, エイズ学研究センター, 特任助教 (80710409)

Research Collaborator MURAKOSHI Hayato  
AKAHOSHI Tomohiro  
Project Period (FY) 2016-04-01 – 2018-03-31
KeywordsHIV-1 / CTL / CD8陽性T細胞 / ナイーブT細胞 / プライミング / STINGリガンド
Outline of Final Research Achievements

HIV-1-specific CD8+ T cells are required for immune suppression of HIV-1 replication and elimination of the viral reservoirs. However, effective priming method of functional HIV-1-specific CD8+ T cells from naïve T cells remains unclear. The present study demonstrated that STING ligand cGAMP effectively induced functional HIV-specific CD8+ T cells with ability to suppress HIV-1 from naive T cells. These finding suggest that STING ligand is useful for AIDS vaccines and cure treatment.

Free Research Field

感染免疫学

URL: 

Published: 2019-03-29  

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