Role of CD4+CD25+FOXP3+ TReg cells on tumor immunity

Not all T cells are effector cells of the anti-tumor immune system. One of the subpopulations of CD4+ T cells that express CD25+ and the transcription factor FOXP3, known as Regulator T cells (TReg), plays an essential role in maintaining tolerance and immune homeostasis preventing autoimmune diseas...

Full description

Bibliographic Details
Main Authors: Agustinus Darmadi Hariyanto, Tiara Bunga Mayang Permata, Soehartati Argadikoesoema Gondhowiardjo
Format: Article
Language:English
Published: Taylor & Francis Group 2021-09-01
Series:Immunological Medicine
Subjects:
Online Access:http://dx.doi.org/10.1080/25785826.2021.1975228
_version_ 1819071369255583744
author Agustinus Darmadi Hariyanto
Tiara Bunga Mayang Permata
Soehartati Argadikoesoema Gondhowiardjo
author_facet Agustinus Darmadi Hariyanto
Tiara Bunga Mayang Permata
Soehartati Argadikoesoema Gondhowiardjo
author_sort Agustinus Darmadi Hariyanto
collection DOAJ
description Not all T cells are effector cells of the anti-tumor immune system. One of the subpopulations of CD4+ T cells that express CD25+ and the transcription factor FOXP3, known as Regulator T cells (TReg), plays an essential role in maintaining tolerance and immune homeostasis preventing autoimmune diseases, minimalize chronic inflammatory diseases by enlisting various immunoregulatory mechanisms. The balance between effector T cells (Teff) and regulator T cells is crucial in determining the outcome of an immune response. Regarding tumors, activation or expansion of TReg cells reduces anti-tumor immunity. TReg cells inhibit the activation of CD4+ and CD8+ T cells and suppress anti-tumor activity in the tumor microenvironment. In addition, TReg cells also promote tumor angiogenesis both directly and indirectly to ensure oxygen and nutrient transport to the tumor. There is accumulating evidence showing a positive result that removing or suppressing TReg cells increases anti-tumor immune response. However, depletion of TReg cells will cause autoimmunity. One strategy to improve or restore tumor immunity is targeted therapy on the dominant effector TReg cells in tumor tissue. Various molecules such as CTLA-4, CD4, CD25, GITR, PD-1, OX40, ICOS are in clinical trials to assess their role in attenuating TReg cells’ function.
first_indexed 2024-12-21T17:20:44Z
format Article
id doaj.art-d55152cdce5a47e6b3b19359dad684a5
institution Directory Open Access Journal
issn 2578-5826
language English
last_indexed 2024-12-21T17:20:44Z
publishDate 2021-09-01
publisher Taylor & Francis Group
record_format Article
series Immunological Medicine
spelling doaj.art-d55152cdce5a47e6b3b19359dad684a52022-12-21T18:56:11ZengTaylor & Francis GroupImmunological Medicine2578-58262021-09-010011410.1080/25785826.2021.19752281975228Role of CD4+CD25+FOXP3+ TReg cells on tumor immunityAgustinus Darmadi Hariyanto0Tiara Bunga Mayang Permata1Soehartati Argadikoesoema Gondhowiardjo2Faculty of Medicine, Department of Radiotherapy, Universitas Indonesia/Cipto Mangunkusumo National General HospitalFaculty of Medicine, Department of Radiotherapy, Universitas Indonesia/Cipto Mangunkusumo National General HospitalFaculty of Medicine, Department of Radiotherapy, Universitas Indonesia/Cipto Mangunkusumo National General HospitalNot all T cells are effector cells of the anti-tumor immune system. One of the subpopulations of CD4+ T cells that express CD25+ and the transcription factor FOXP3, known as Regulator T cells (TReg), plays an essential role in maintaining tolerance and immune homeostasis preventing autoimmune diseases, minimalize chronic inflammatory diseases by enlisting various immunoregulatory mechanisms. The balance between effector T cells (Teff) and regulator T cells is crucial in determining the outcome of an immune response. Regarding tumors, activation or expansion of TReg cells reduces anti-tumor immunity. TReg cells inhibit the activation of CD4+ and CD8+ T cells and suppress anti-tumor activity in the tumor microenvironment. In addition, TReg cells also promote tumor angiogenesis both directly and indirectly to ensure oxygen and nutrient transport to the tumor. There is accumulating evidence showing a positive result that removing or suppressing TReg cells increases anti-tumor immune response. However, depletion of TReg cells will cause autoimmunity. One strategy to improve or restore tumor immunity is targeted therapy on the dominant effector TReg cells in tumor tissue. Various molecules such as CTLA-4, CD4, CD25, GITR, PD-1, OX40, ICOS are in clinical trials to assess their role in attenuating TReg cells’ function.http://dx.doi.org/10.1080/25785826.2021.1975228tregregulatory t cellsanti-tumor immunityimmunotherapytreg-targeting therapy
spellingShingle Agustinus Darmadi Hariyanto
Tiara Bunga Mayang Permata
Soehartati Argadikoesoema Gondhowiardjo
Role of CD4+CD25+FOXP3+ TReg cells on tumor immunity
Immunological Medicine
treg
regulatory t cells
anti-tumor immunity
immunotherapy
treg-targeting therapy
title Role of CD4+CD25+FOXP3+ TReg cells on tumor immunity
title_full Role of CD4+CD25+FOXP3+ TReg cells on tumor immunity
title_fullStr Role of CD4+CD25+FOXP3+ TReg cells on tumor immunity
title_full_unstemmed Role of CD4+CD25+FOXP3+ TReg cells on tumor immunity
title_short Role of CD4+CD25+FOXP3+ TReg cells on tumor immunity
title_sort role of cd4 cd25 foxp3 treg cells on tumor immunity
topic treg
regulatory t cells
anti-tumor immunity
immunotherapy
treg-targeting therapy
url http://dx.doi.org/10.1080/25785826.2021.1975228
work_keys_str_mv AT agustinusdarmadihariyanto roleofcd4cd25foxp3tregcellsontumorimmunity
AT tiarabungamayangpermata roleofcd4cd25foxp3tregcellsontumorimmunity
AT soehartatiargadikoesoemagondhowiardjo roleofcd4cd25foxp3tregcellsontumorimmunity