Imbalance of TH17/TREG cells in Tunisian patients with systemic sclerosis

IF 3.2 3区 医学 Q1 MEDICINE, GENERAL & INTERNAL Presse Medicale Pub Date : 2023-12-30 DOI:10.1016/j.lpm.2023.104221
Gabsi Amira , Dlala Akram , Missaoui Fadoua , Neili Bilel , Boutaba Alya , Ben salem Khalil , Smiti Khanfir Monia , Said Fatma , Houman Mohamed Habib , Bardin Nathalie , Triki Marrakchi Raja
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Abstract

Fibrosis is a pathological manifestation in which connective tissue replaces normal one. It can affect many tissues from the skin to internal organs such as the lungs. Manifestations of pulmonary involvement can be pulmonary arterial hypertension or pulmonary fibrosis. The latter one is currently the leading cause of death in various autoimmune diseases, including systemic sclerosis.

Our study group consists of 50 patients with systemic sclerosis: 24 with limited cutaneous form and 26 with diffuse cutaneous form. This cohort was compared to 50 healthy controls (age and sex matched); our aim is to explore the distribution of TH17 cells (TH17) as well as regulatory T cells (TREG) and study their correlation with the disease's progress. Our results show an increase for IL17A in patients compared to controls and that this increase is correlated with a specific clinical involvement: Pulmonary fibrosis. This correlation suggests a crucial role of IL17A in fibrosis especially in systemic sclerosis. In addition, we have shown that the percentages of TH17 cells are higher in patients; however, the percentages of TREG cells are similar between patients and controls. A study of TREG cell activity showed that TREG lost suppressive activity by inactivating the FOXP3 transcription factor. This proves that despite their presence, TREG does not adequately carry out their regulatory activity. Finally, we analyzed the correlation between TH17/TREG and clinical damage; the results show a positive correlation with pulmonary involvement proving the role of TH17/TREG balance in induced fibrosis in systemic sclerosis. No significative difference was observed, for all the parameters, between the two different forms of the disease.

In conclusion, the results associated with the TH17/TREG scale and their correlations with fibrosis in systemic sclerosis open a way for new tools to manage this autoimmune disease, which up to today has neither treatment nor accurate diagnosis.

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突尼斯系统性硬化症患者体内 TH17/TREG 细胞失衡。
纤维化是结缔组织取代正常组织的一种病理表现。它可以影响从皮肤到肺部等内脏器官的许多组织。肺部受累的表现可以是肺动脉高压或肺纤维化。后者是包括系统性硬化症在内的各种自身免疫性疾病的主要致死原因。我们的研究小组由 50 名系统性硬化症患者组成,其中 24 人患有局限性皮肤病,26 人患有弥漫性皮肤病。我们的目的是探索 TH17 细胞(TH17)和调节性 T 细胞(TREG)的分布情况,并研究它们与疾病进展的相关性。我们的研究结果表明,与对照组相比,患者体内的 IL17A 有所增加,而且这种增加与特定的临床症状有关:肺纤维化。这种相关性表明,IL17A 在纤维化过程中起着至关重要的作用,尤其是在系统性硬化症中。此外,我们还发现,患者体内 TH17 细胞的百分比更高;但患者和对照组之间 TREG 细胞的百分比相似。对 TREG 细胞活性的研究表明,TREG 通过使 FOXP3 转录因子失活而失去抑制活性。这证明,尽管 TREG 存在,但它们并不能充分发挥其调节活性。最后,我们分析了 TH17/TREG 与临床损害之间的相关性;结果显示,TH17/TREG 与肺部受累呈正相关,这证明了 TH17/TREG 平衡在诱导系统性硬化症纤维化中的作用。在两种不同形式的疾病之间,所有参数均无显著差异。总之,TH17/TREG 量表的相关结果及其与系统性硬化症纤维化的相关性为管理这种自身免疫性疾病提供了新的工具,这种疾病至今既没有治疗方法,也没有准确的诊断。
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来源期刊
Presse Medicale
Presse Medicale 医学-医学:内科
自引率
3.70%
发文量
40
审稿时长
43 days
期刊介绍: Seule revue médicale "généraliste" de haut niveau, La Presse Médicale est l''équivalent francophone des grandes revues anglosaxonnes de publication et de formation continue. A raison d''un numéro par mois, La Presse Médicale vous offre une double approche éditoriale : - des publications originales (articles originaux, revues systématiques, cas cliniques) soumises à double expertise, portant sur les avancées médicales les plus récentes ; - une partie orientée vers la FMC, vous propose une mise à jour permanente et de haut niveau de vos connaissances, sous forme de dossiers thématiques et de mises au point dans les principales spécialités médicales, pour vous aider à optimiser votre formation.
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