Academic Journal
POS0326 ROLE OF THE IL-25 / IL-17RB AXIS IN TH9 POLARIZATION IN PATIENTS WITH PROGRESSIVE SYSTEMIC SCLEROSIS
العنوان: | POS0326 ROLE OF THE IL-25 / IL-17RB AXIS IN TH9 POLARIZATION IN PATIENTS WITH PROGRESSIVE SYSTEMIC SCLEROSIS |
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المؤلفون: | La Barbera, L., Lo Pizzo, M., DI Liberto, D., Schinocca, C., Ruscitti, P., Giacomelli, R., Dieli, F., Ciccia, F., Guggino, G. |
المصدر: | Annals of the Rheumatic Diseases ; volume 80, issue Suppl 1, page 390-391 ; ISSN 0003-4967 1468-2060 |
بيانات النشر: | BMJ |
سنة النشر: | 2021 |
الوصف: | Background: Systemic sclerosis (SSc) is an inflammatory connective tissue disease leading to chronic and progressive fibrosis, typically affecting the skin and internal organs. The alteration of both innate and adaptive immune responses plays a pivotal role in SSc pathophysiology, although it has not yet been fully elucidated [1]. Recent findings have demonstrated interleukin (IL)-9 overexpression and significant group 2 innate lymphoid cells (ILC2) expansion in patients with SSc. Th9-ILC2-mast cells axis seems to be involved in SSc tissue damage and in the induction of fibrosis [2]. Activation and production of IL-9 by Th9 cells are promoted by transforming growth factor (TGF)-β, thymic stromal lymphopoietin (TSLP), IL-25 and IL-33. Thus, the IL-25 / IL-17RB pathway would act as a key player in SSc. Objectives: The purpose of this study was to evaluate the role of the IL-25 / IL-17RB axis as a driver in Th9 polarization and ILC2 expansion and polarization in SSc patients. Methods: 26 patients were enrolled in this study. Peripheral blood and skin biopsy specimens were obtained from SSc patients. PBMCs were isolated and incubated with and without recombinant (r)IL-25 for 24-48-72 hours and the frequencies of Th9 cells, Th17 cells and ILC2 were assessed by flow cytometry analysis. Moreover, the ex vivo expression of IL-17RB in ILC2 was also assessed. Immunofluorescence analysis was performed on biopsy skin samples to evaluate IL-17RB expression in ILC2. Results: In SSc samples, Th9 cells frequency progressively increased after stimulation with rIL-25, compared to healthy controls in which IL-9 frequency decreased over time regardless of rIL-25. Simultaneously, we evaluated the role of the IL-25 / IL-17RB axis in Th17 cells. In the SSc pool, the initially low rate of IL-17 increased at 72 hours after stimulation with rIL-25. In unstimulated SSc samples, the initially higher IL-17 rate decreased at 72 hours; conversely, it was consistently low in healthy controls, at both baseline and stimulated conditions. Our ... |
نوع الوثيقة: | article in journal/newspaper |
اللغة: | English |
DOI: | 10.1136/annrheumdis-2021-eular.3814 |
الاتاحة: | http://dx.doi.org/10.1136/annrheumdis-2021-eular.3814 https://syndication.highwire.org/content/doi/10.1136/annrheumdis-2021-eular.3814 |
رقم الانضمام: | edsbas.B638D33D |
قاعدة البيانات: | BASE |
DOI: | 10.1136/annrheumdis-2021-eular.3814 |
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