{"title":"The role of regulatory T cells in preventing the development of drug hypersensitivity reactions.","authors":"Lonnie MacDonald, Megan Mitchell, Paul Thomson","doi":"10.1097/ACI.0000000000001083","DOIUrl":null,"url":null,"abstract":"<p><strong>Purpose of review: </strong>T-cell-mediated drug hypersensitivity reactions represent a major impediment to the drug discovery process whilst presenting a significant burden to the healthcare sector. These reactions are predominantly facilitated by the adaptive immune system, yet the equilibrium of immune tolerance appears to be a significant determinant in whether an individual will experience a hypersensitivity reaction to a therapeutic.</p><p><strong>Recent findings: </strong>Indeed, regulatory T cells (Tregs) play a significant part in diminishing an immune response by CD4+ and CD8+ T cells and preventing autoimmunity by keeping an immune response in check. These cell subsets have been observed to be upregulated in times of immune activation, and unsurprisingly, their impairment has been associated in tandem with dysregulated immune responses contributing to the sliding scale of drug hypersensitivity.</p><p><strong>Summary: </strong>It is becoming increasingly evident that the fine balance of immune regulation significantly impacts on drug hypersensitivity reactions. As the area progresses, it will be interesting to assess whether therapies targeting Tregs hold the key to maintaining the synergy required to prevent the onset of drug hypersensitivity reactions.</p>","PeriodicalId":10956,"journal":{"name":"Current Opinion in Allergy and Clinical Immunology","volume":"25 4","pages":"221-229"},"PeriodicalIF":3.0000,"publicationDate":"2025-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current Opinion in Allergy and Clinical Immunology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1097/ACI.0000000000001083","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/6/11 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"ALLERGY","Score":null,"Total":0}
引用次数: 0
Abstract
Purpose of review: T-cell-mediated drug hypersensitivity reactions represent a major impediment to the drug discovery process whilst presenting a significant burden to the healthcare sector. These reactions are predominantly facilitated by the adaptive immune system, yet the equilibrium of immune tolerance appears to be a significant determinant in whether an individual will experience a hypersensitivity reaction to a therapeutic.
Recent findings: Indeed, regulatory T cells (Tregs) play a significant part in diminishing an immune response by CD4+ and CD8+ T cells and preventing autoimmunity by keeping an immune response in check. These cell subsets have been observed to be upregulated in times of immune activation, and unsurprisingly, their impairment has been associated in tandem with dysregulated immune responses contributing to the sliding scale of drug hypersensitivity.
Summary: It is becoming increasingly evident that the fine balance of immune regulation significantly impacts on drug hypersensitivity reactions. As the area progresses, it will be interesting to assess whether therapies targeting Tregs hold the key to maintaining the synergy required to prevent the onset of drug hypersensitivity reactions.
期刊介绍:
This reader-friendly, bimonthly resource provides a powerful, broad-based perspective on the most important advances from throughout the world literature. Featuring renowned guest editors and focusing exclusively on one to three topics, every issue of Current Opinion in Allergy and Clinical Immunology delivers unvarnished, expert assessments of developments from the previous year. Insightful editorials and on-the-mark invited reviews cover key subjects such as upper airway disease; mechanisms of allergy and adult asthma; paediatric asthma and development of atopy; food and drug allergies; and immunotherapy.