Dobrican-Băruța Carmen-Teodora, Deleanu Diana Mihaela, Muntean Ioana Adriana, Pintea Irena, Florea Cristian Marius, Filip Gabriela Adriana
"Iuliu Hatieganu" University of Medicine and Pharmacy, Department of Allergology and Clinical Immunology, 400012 Cluj-Napoca, Romania.
"Iuliu Hatieganu" University of Medicine and Pharmacy, Department of Cardiology, 400012 Cluj-Napoca, Romania.
J Clin Med. 2023 Sep 13;12(18):5957. doi: 10.3390/jcm12185957.
(1) Background: This study aimed to evaluate the implications of interleukin-31 (IL-31) in the pathogenesis of chronic spontaneous urticaria (CSU) and to assess the differences that occur between its serum values compared to controls. Additionally, the serum IL-31 levels were measured alongside other clinical and paraclinical parameters that were identified in the patients to understand its immunological importance in this skin disease and to determine if it could potentially serve as a therapeutic target in CSU in the future. (2) Methods: The serum levels of IL-31 were estimated in 50 patients diagnosed with CSU according to the accepted international guidelines. Additionally, 38 controls who had not experienced any episodes of urticaria during their lifetime were included. (3) Results: Significantly elevated serum IL-31 levels were observed in CSU patients compared to the controls ( < 0.0001). Although no direct correlations were found between IL-31 and inflammatory markers (erythrocyte sedimentation rate (ESR), C-reactive protein (CRP)), eosinophils, or total immunoglobulins E (IgE), significant differences in IL-31 levels were identified based on CSU severity, quality of life impact, itch intensity, and response to histamine H1 receptor antagonists (H1 antihistamines) ( < 0.05 for all). (4) Conclusions: Our findings underscore that IL-31 is not directly associated with general inflammation, eosinophilic response, or atopy in CSU. Nevertheless, its expression is influenced by key disease characteristics: severity, pruritus, and H1 antihistamine response. This investigation provides essential insights into CSU pathogenesis, potentially leading to novel therapeutic interventions. An enhanced understanding of these mechanisms is crucial due to the limitations of current treatment modalities in terms of fully managing CSU symptoms.
(1)背景:本研究旨在评估白细胞介素-31(IL-31)在慢性自发性荨麻疹(CSU)发病机制中的作用,并评估其血清值与对照组相比的差异。此外,还测量了患者血清IL-31水平以及其他临床和辅助临床参数,以了解其在这种皮肤病中的免疫重要性,并确定其未来是否有可能成为CSU的治疗靶点。(2)方法:根据公认的国际指南,对50例诊断为CSU的患者进行血清IL-31水平评估。此外,纳入38名一生中未经历过任何荨麻疹发作的对照者。(3)结果:与对照组相比,CSU患者血清IL-31水平显著升高(<0.0001)。虽然未发现IL-31与炎症标志物(红细胞沉降率(ESR)、C反应蛋白(CRP))、嗜酸性粒细胞或总免疫球蛋白E(IgE)之间存在直接相关性,但根据CSU严重程度、生活质量影响、瘙痒强度和对组胺H1受体拮抗剂(H1抗组胺药)的反应,IL-31水平存在显著差异(所有均<0.05)。(4)结论:我们的研究结果强调,IL-31与CSU中的全身炎症、嗜酸性粒细胞反应或特应性无直接关联。然而,其表达受关键疾病特征影响:严重程度、瘙痒和H1抗组胺药反应。本研究为CSU发病机制提供了重要见解,可能导致新的治疗干预措施。鉴于目前治疗方式在全面控制CSU症状方面的局限性,深入了解这些机制至关重要。