Different subpopulations of regulatory T cells in human autoimmune disease, transplantation, and tumor immunity. Issue 2 (21st April 2022)
- Record Type:
- Journal Article
- Title:
- Different subpopulations of regulatory T cells in human autoimmune disease, transplantation, and tumor immunity. Issue 2 (21st April 2022)
- Main Title:
- Different subpopulations of regulatory T cells in human autoimmune disease, transplantation, and tumor immunity
- Authors:
- Jiang, Zhongyi
Zhu, Haitao
Wang, Pusen
Que, Weitao
Zhong, Lin
Li, Xiao‐Kang
Du, Futian - Abstract:
- Abstract: CD4 + CD25 + regulatory T cells (Tregs), a subpopulation of naturally CD4 + T cells that characteristically express transcription factor Forkhead box P3 (FOXP3), play a pivotal role in the maintenance of immune homeostasis and the prevention of autoimmunity. With the development of biological technology, the understanding of plasticity and stability of Tregs has been further developed. Recent studies have suggested that human Tregs are functionally and phenotypically diverse. The functions and mechanisms of different phenotypes of Tregs in different disease settings, such as tumor microenvironment, autoimmune diseases, and transplantation, have gradually become hot spots of immunology research that arouse extensive attention. Among the complex functions, CD4 + CD25 + FOXP3 + Tregs possess a potent immunosuppressive capacity and can produce various cytokines, such as IL‐2, IL‐10, and TGF‐β, to regulate immune homeostasis. They can alleviate the progression of diseases by resisting inflammatory immune responses, whereas promoting the poor prognosis of diseases by helping cells evade immune surveillance or suppressing effector T cells activity. Therefore, methods for targeting Tregs to regulate their functions in the immune microenvironment, such as depleting them to strengthen tumor immunity or expanding them to treat immunological diseases, need to be developed. Here, we discuss that different subpopulations of Tregs are essential for the development ofAbstract: CD4 + CD25 + regulatory T cells (Tregs), a subpopulation of naturally CD4 + T cells that characteristically express transcription factor Forkhead box P3 (FOXP3), play a pivotal role in the maintenance of immune homeostasis and the prevention of autoimmunity. With the development of biological technology, the understanding of plasticity and stability of Tregs has been further developed. Recent studies have suggested that human Tregs are functionally and phenotypically diverse. The functions and mechanisms of different phenotypes of Tregs in different disease settings, such as tumor microenvironment, autoimmune diseases, and transplantation, have gradually become hot spots of immunology research that arouse extensive attention. Among the complex functions, CD4 + CD25 + FOXP3 + Tregs possess a potent immunosuppressive capacity and can produce various cytokines, such as IL‐2, IL‐10, and TGF‐β, to regulate immune homeostasis. They can alleviate the progression of diseases by resisting inflammatory immune responses, whereas promoting the poor prognosis of diseases by helping cells evade immune surveillance or suppressing effector T cells activity. Therefore, methods for targeting Tregs to regulate their functions in the immune microenvironment, such as depleting them to strengthen tumor immunity or expanding them to treat immunological diseases, need to be developed. Here, we discuss that different subpopulations of Tregs are essential for the development of immunotherapeutic strategies involving Tregs in human diseases. Abstract : Forkhead box P3 (FOXP3) regulatory T cells (Tregs) play a pivotal role in the maintenance of immune homeostasis and prevention of autoimmunity. Recent studies have suggested that human Tregs are functionally and phenotypically diverse. Here, we discuss that different Tregs subsets are essential for the development of immunotherapeutic strategies involving Tregs in human diseases. … (more)
- Is Part Of:
- MedComm. Volume 3:Issue 2(2022)
- Journal:
- MedComm
- Issue:
- Volume 3:Issue 2(2022)
- Issue Display:
- Volume 3, Issue 2 (2022)
- Year:
- 2022
- Volume:
- 3
- Issue:
- 2
- Issue Sort Value:
- 2022-0003-0002-0000
- Page Start:
- n/a
- Page End:
- n/a
- Publication Date:
- 2022-04-21
- Subjects:
- autoimmune disease -- FOXP3 -- regulatory T cell -- subpopulation -- transplantation -- tumor immunity
610 - Journal URLs:
- http://onlinelibrary.wiley.com/ ↗
- DOI:
- 10.1002/mco2.137 ↗
- Languages:
- English
- ISSNs:
- 2688-2663
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 21835.xml