Regulatory T Cells: Barriers of Immune Infiltration Into the Tumor Microenvironment
Regulatory T cells (Tregs) are key immunosuppressive cells that promote tumor growth by hindering the effector immune response. Tregs utilize multiple suppressive mechanisms to inhibit pro-inflammatory responses within the tumor microenvironment (TME) by inhibition of effector function and immune ce...
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doaj-124781edeefb493b9afec393691b08942021-06-10T07:28:32ZengFrontiers Media S.A.Frontiers in Immunology1664-32242021-06-011210.3389/fimmu.2021.702726702726Regulatory T Cells: Barriers of Immune Infiltration Into the Tumor MicroenvironmentEllen N. Scott0Ellen N. Scott1Ellen N. Scott2Angela M. Gocher3Angela M. Gocher4Creg J. Workman5Creg J. Workman6Dario A. A. Vignali7Dario A. A. Vignali8Dario A. A. Vignali9Department of Immunology, University of Pittsburgh School of Medicine, Pittsburgh, PA, United StatesTumor Microenvironment Center, University of Pittsburgh Medical Center (UPMC) Hillman Cancer Center, Pittsburgh, PA, United StatesGraduate Program of Microbiology and Immunology, University of Pittsburgh School of Medicine, Pittsburgh, PA, United StatesDepartment of Immunology, University of Pittsburgh School of Medicine, Pittsburgh, PA, United StatesTumor Microenvironment Center, University of Pittsburgh Medical Center (UPMC) Hillman Cancer Center, Pittsburgh, PA, United StatesDepartment of Immunology, University of Pittsburgh School of Medicine, Pittsburgh, PA, United StatesTumor Microenvironment Center, University of Pittsburgh Medical Center (UPMC) Hillman Cancer Center, Pittsburgh, PA, United StatesDepartment of Immunology, University of Pittsburgh School of Medicine, Pittsburgh, PA, United StatesTumor Microenvironment Center, University of Pittsburgh Medical Center (UPMC) Hillman Cancer Center, Pittsburgh, PA, United StatesCancer Immunology and Immunotherapy Program, UPMC Hillman Cancer Center, Pittsburgh, PA, United StatesRegulatory T cells (Tregs) are key immunosuppressive cells that promote tumor growth by hindering the effector immune response. Tregs utilize multiple suppressive mechanisms to inhibit pro-inflammatory responses within the tumor microenvironment (TME) by inhibition of effector function and immune cell migration, secretion of inhibitory cytokines, metabolic disruption and promotion of metastasis. In turn, Tregs are being targeted in the clinic either alone or in combination with other immunotherapies, in efforts to overcome the immunosuppressive TME and increase anti-tumor effects. However, it is now appreciated that Tregs not only suppress cells intratumorally via direct engagement, but also serve as key interactors in the peritumor, stroma, vasculature and lymphatics to limit anti-tumor immune responses prior to tumor infiltration. We will review the suppressive mechanisms that Tregs utilize to alter immune and non-immune cells outside and within the TME and discuss how these mechanisms collectively allow Tregs to create and promote a physical and biological barrier, resulting in an immune-excluded or limited tumor microenvironment.https://www.frontiersin.org/articles/10.3389/fimmu.2021.702726/fullregulatory T cells (Treg)immune infiltrationtumor microenvironmentcancervasculaturestroma |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Ellen N. Scott Ellen N. Scott Ellen N. Scott Angela M. Gocher Angela M. Gocher Creg J. Workman Creg J. Workman Dario A. A. Vignali Dario A. A. Vignali Dario A. A. Vignali |
spellingShingle |
Ellen N. Scott Ellen N. Scott Ellen N. Scott Angela M. Gocher Angela M. Gocher Creg J. Workman Creg J. Workman Dario A. A. Vignali Dario A. A. Vignali Dario A. A. Vignali Regulatory T Cells: Barriers of Immune Infiltration Into the Tumor Microenvironment Frontiers in Immunology regulatory T cells (Treg) immune infiltration tumor microenvironment cancer vasculature stroma |
author_facet |
Ellen N. Scott Ellen N. Scott Ellen N. Scott Angela M. Gocher Angela M. Gocher Creg J. Workman Creg J. Workman Dario A. A. Vignali Dario A. A. Vignali Dario A. A. Vignali |
author_sort |
Ellen N. Scott |
title |
Regulatory T Cells: Barriers of Immune Infiltration Into the Tumor Microenvironment |
title_short |
Regulatory T Cells: Barriers of Immune Infiltration Into the Tumor Microenvironment |
title_full |
Regulatory T Cells: Barriers of Immune Infiltration Into the Tumor Microenvironment |
title_fullStr |
Regulatory T Cells: Barriers of Immune Infiltration Into the Tumor Microenvironment |
title_full_unstemmed |
Regulatory T Cells: Barriers of Immune Infiltration Into the Tumor Microenvironment |
title_sort |
regulatory t cells: barriers of immune infiltration into the tumor microenvironment |
publisher |
Frontiers Media S.A. |
series |
Frontiers in Immunology |
issn |
1664-3224 |
publishDate |
2021-06-01 |
description |
Regulatory T cells (Tregs) are key immunosuppressive cells that promote tumor growth by hindering the effector immune response. Tregs utilize multiple suppressive mechanisms to inhibit pro-inflammatory responses within the tumor microenvironment (TME) by inhibition of effector function and immune cell migration, secretion of inhibitory cytokines, metabolic disruption and promotion of metastasis. In turn, Tregs are being targeted in the clinic either alone or in combination with other immunotherapies, in efforts to overcome the immunosuppressive TME and increase anti-tumor effects. However, it is now appreciated that Tregs not only suppress cells intratumorally via direct engagement, but also serve as key interactors in the peritumor, stroma, vasculature and lymphatics to limit anti-tumor immune responses prior to tumor infiltration. We will review the suppressive mechanisms that Tregs utilize to alter immune and non-immune cells outside and within the TME and discuss how these mechanisms collectively allow Tregs to create and promote a physical and biological barrier, resulting in an immune-excluded or limited tumor microenvironment. |
topic |
regulatory T cells (Treg) immune infiltration tumor microenvironment cancer vasculature stroma |
url |
https://www.frontiersin.org/articles/10.3389/fimmu.2021.702726/full |
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