Matthias Hose , Vivien Blietschau , Fabian Schumacher , Anne Ninnemann , Eyad Naser , Julia Falkenstein , Alexander Carpinteiro , Burkhard Kleuser , Jan Buer , Astrid M. Westendorf , Ulrike Bingel , Daniel Müller , Wiebke Hansen
{"title":"Influence of amitriptyline therapy on T cell phenotype in chronic pain patients","authors":"Matthias Hose , Vivien Blietschau , Fabian Schumacher , Anne Ninnemann , Eyad Naser , Julia Falkenstein , Alexander Carpinteiro , Burkhard Kleuser , Jan Buer , Astrid M. Westendorf , Ulrike Bingel , Daniel Müller , Wiebke Hansen","doi":"10.1016/j.biopha.2025.118529","DOIUrl":null,"url":null,"abstract":"<div><div>Chronic pain (CP) is a major health issue globally, affecting millions and resulting in a significant healthcare burden. Although amitriptyline is widely used to manage CP, its immunomodulatory effects during pain therapy, especially on T cell phenotypes, remain unclear. In this study, we explored how amitriptyline alters T cell phenotypes in CP patients. Therefore, we analyzed the expression profile of peripheral T cells from patients suffering from CP before and three months after amitriptyline therapy in comparison to healthy volunteers. Additionally, the impact of amitriptyline on the T cell phenotype was investigated <em>in vitro</em>. Our results revealed that amitriptyline interferes with production of the pro-inflammatory cytokine interferon (IFN)-γ and elevates the anti-inflammatory cytokine interleukin (IL)-10 as well as frequencies of immunosuppressive regulatory T cells, in particular in patients with improved pain after therapy. Hence, amitriptyline therapy affects the adaptive immune response, which might contribute to pain relief through an immune-mediated mechanism.</div></div>","PeriodicalId":8966,"journal":{"name":"Biomedicine & Pharmacotherapy","volume":"191 ","pages":"Article 118529"},"PeriodicalIF":7.5000,"publicationDate":"2025-09-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biomedicine & Pharmacotherapy","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0753332225007231","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MEDICINE, RESEARCH & EXPERIMENTAL","Score":null,"Total":0}
引用次数: 0
Abstract
Chronic pain (CP) is a major health issue globally, affecting millions and resulting in a significant healthcare burden. Although amitriptyline is widely used to manage CP, its immunomodulatory effects during pain therapy, especially on T cell phenotypes, remain unclear. In this study, we explored how amitriptyline alters T cell phenotypes in CP patients. Therefore, we analyzed the expression profile of peripheral T cells from patients suffering from CP before and three months after amitriptyline therapy in comparison to healthy volunteers. Additionally, the impact of amitriptyline on the T cell phenotype was investigated in vitro. Our results revealed that amitriptyline interferes with production of the pro-inflammatory cytokine interferon (IFN)-γ and elevates the anti-inflammatory cytokine interleukin (IL)-10 as well as frequencies of immunosuppressive regulatory T cells, in particular in patients with improved pain after therapy. Hence, amitriptyline therapy affects the adaptive immune response, which might contribute to pain relief through an immune-mediated mechanism.
期刊介绍:
Biomedicine & Pharmacotherapy stands as a multidisciplinary journal, presenting a spectrum of original research reports, reviews, and communications in the realms of clinical and basic medicine, as well as pharmacology. The journal spans various fields, including Cancer, Nutriceutics, Neurodegenerative, Cardiac, and Infectious Diseases.