Christine M. Wardell, Dominic A. Boardman, Megan K. Levings
{"title":"Harnessing the biology of regulatory T cells to treat disease","authors":"Christine M. Wardell, Dominic A. Boardman, Megan K. Levings","doi":"10.1038/s41573-024-01089-x","DOIUrl":null,"url":null,"abstract":"<p>Regulatory T (T<sub>reg</sub>) cells are a suppressive subset of CD4<sup>+</sup> T cells that maintain immune homeostasis and restrain inflammation. Three decades after their discovery, the promise of strategies to harness T<sub>reg</sub> cells for therapy has never been stronger. Multiple clinical trials seeking to enhance endogenous T<sub>reg</sub> cells or deliver them as a cell-based therapy have been performed and hint at signs of success, as well as to important limitations and unanswered questions. Strategies to deplete T<sub>reg</sub> cells in cancer are also in active clinical testing. Furthermore, multi-dimensional methods to interrogate the biology of T<sub>reg</sub> cells are leading to a refined understanding of T<sub>reg</sub> cell biology and new approaches to harness tissue-specific functions for therapy. A new generation of T<sub>reg</sub> cell clinical trials is now being fuelled by advances in nanomedicine and synthetic biology, seeking more precise ways to tailor T<sub>reg</sub> cell function. This Review will discuss recent advances in our understanding of human T<sub>reg</sub> cell biology, with a focus on mechanisms of action and strategies to assess outcomes of T<sub>reg</sub> cell-targeted therapies. It highlights results from recent clinical trials aiming to enhance or inhibit T<sub>reg</sub> cell activity in a variety of diseases, including allergy, transplantation, autoimmunity and cancer, and discusses ongoing strategies to refine these approaches.</p>","PeriodicalId":18847,"journal":{"name":"Nature Reviews Drug Discovery","volume":"20 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-12-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Nature Reviews Drug Discovery","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1038/s41573-024-01089-x","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Regulatory T (Treg) cells are a suppressive subset of CD4+ T cells that maintain immune homeostasis and restrain inflammation. Three decades after their discovery, the promise of strategies to harness Treg cells for therapy has never been stronger. Multiple clinical trials seeking to enhance endogenous Treg cells or deliver them as a cell-based therapy have been performed and hint at signs of success, as well as to important limitations and unanswered questions. Strategies to deplete Treg cells in cancer are also in active clinical testing. Furthermore, multi-dimensional methods to interrogate the biology of Treg cells are leading to a refined understanding of Treg cell biology and new approaches to harness tissue-specific functions for therapy. A new generation of Treg cell clinical trials is now being fuelled by advances in nanomedicine and synthetic biology, seeking more precise ways to tailor Treg cell function. This Review will discuss recent advances in our understanding of human Treg cell biology, with a focus on mechanisms of action and strategies to assess outcomes of Treg cell-targeted therapies. It highlights results from recent clinical trials aiming to enhance or inhibit Treg cell activity in a variety of diseases, including allergy, transplantation, autoimmunity and cancer, and discusses ongoing strategies to refine these approaches.