Last Updated: 22/12/2025

Induction mechanisms and the regulatory roles of IL-27-producing regulatory T cells during malaria infection

Objectives

*Original title and text were machine translated from Japanese

This project aimed to study antigen recognition of Tr27 cells, mechanisms underlying their induction and their regulatory roles during infection.

Principal Institution

Nagasaki University, Japan

Principal Investigators / Focal Persons

Katsuyuki Yui

Rationale and Abstract

Malaria patients are known to exhibit reduced immune responses, although its mechanisms are unknown. Using a mouse model, it was previously reported CD4+ T cells that inhibit the immune responses in IL-27 dependent manner during malaria infection, and named them Tr27 cells. Data suggested that specific Th1 cells and Tr27 cells recognize distinct Plasmodium antigens. Furthermore, we produced a mouse model to monitor IL-27 expression with a fluorescent protein and conditional gene knock-out mice that lack IL-27 in specific cell populations. These tools are powerful in studying the induction and function of Tr27 cells during infection with malaria parasites.

Date

Apr 2016 — Mar 2019

Total Project Funding

$158,891

Funding Details
Country / Project Site(s)

Japan

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