CRSwNP患者源性3D鼻球体显示Dupilumab治疗后上皮改变:初步报告。

IF 4 Q2 MEDICINE, RESEARCH & EXPERIMENTAL
Nadia Lobello, Giovanna Lucia Piazzetta, Corrado Pelaia, Mariaimmacolata Preianò, Nicola Lombardo, Emanuela Chiarella
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引用次数: 0

摘要

慢性鼻窦炎伴鼻息肉(CRSwNP)是一种与上皮功能障碍和粘膜屏障完整性受损相关的2型炎症性疾病。Dupilumab是一种IL-4受体α拮抗剂,已显示出临床疗效,但其对鼻上皮细胞的影响尚不清楚。先进的体外模型,如3D球体培养可以提供对治疗下上皮组织的深入了解。我们使用从三个患者组获得的鼻上皮细胞进行了初步研究:使用Dupilumab治疗16周的CRSwNP (n = 3),未治疗的CRSwNP (n = 3)和鼻甲肥大对照组(n = 3)。采用酶解法分离细胞,用促球培养基在超低附着板上培养,观察细胞的球形形成情况。使用相衬显微镜进行观察。由于样本量有限,资料采用定性分析,未进行统计检验。对照细胞形成致密的球状体,而未经处理的CRSwNP细胞未能形成结构球状体,仅显示聚集体。dupilumab治疗患者的细胞产生组织良好的球体,表明上皮组织得到改善。观察到偶尔的地表运动,但没有定量评估。没有进行分子或超微结构分析来证实机制假设。我们的初步研究结果表明,Dupilumab治疗可能与CRSwNP中上皮组织的改善有关,如3D培养中的球体形成所示。然而,这些观察是初步的,并基于一个小的横断面队列。未来的研究应包括纵向取样、功能分析和分子分析,以确认机制并验证这些结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Patient-derived 3D nasal spheroids reveal epithelial changes following Dupilumab therapy in CRSwNP: a preliminary report.

Chronic rhinosinusitis with nasal polyps (CRSwNP) is a type 2 inflammatory disease associated with epithelial dysfunction and impaired mucosal barrier integrity. Dupilumab, an IL-4 receptor alpha antagonist, has shown clinical efficacy, but its cellular effects on nasal epithelium remain poorly understood. Advanced in vitro models such as 3D spheroid cultures may provide insight into epithelial organization under treatment. We conducted a preliminary study using nasal epithelial cells obtained from three patient groups: CRSwNP treated with Dupilumab for 16 weeks (n = 3), untreated CRSwNP (n = 3), and turbinate hypertrophy controls (n = 3). Cells were isolated by enzymatic digestion and cultured in ultra-low attachment plates using sphere-promoting medium to assess spheroid formation. Observations were performed using phase-contrast microscopy. Due to the limited sample size, data were analyzed qualitatively without statistical testing. Control cells formed compact spheroids, while untreated CRSwNP cells failed to generate structured spheroids, showing only aggregates. Cells from Dupilumab-treated patients produced well-organized spheroids, suggesting improved epithelial organization. Occasional surface movement was observed but not quantitatively assessed. No molecular or ultrastructural assays were performed to confirm mechanistic hypotheses. Our preliminary findings indicate that Dupilumab treatment may be associated with improved epithelial organization in CRSwNP, as shown by spheroid formation in 3D culture. However, these observations are preliminary and based on a small cross-sectional cohort. Future studies should include longitudinal sampling, functional assays, and molecular analyses to confirm mechanisms and validate these results.

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来源期刊
Tissue Barriers
Tissue Barriers MEDICINE, RESEARCH & EXPERIMENTAL-
CiteScore
6.60
自引率
6.50%
发文量
25
期刊介绍: Tissue Barriers is the first international interdisciplinary journal that focuses on the architecture, biological roles and regulation of tissue barriers and intercellular junctions. We publish high quality peer-reviewed articles that cover a wide range of topics including structure and functions of the diverse and complex tissue barriers that occur across tissue and cell types, including the molecular composition and dynamics of polarized cell junctions and cell-cell interactions during normal homeostasis, injury and disease state. Tissue barrier formation in regenerative medicine and restoration of tissue and organ function is also of interest. Tissue Barriers publishes several categories of articles including: Original Research Papers, Short Communications, Technical Papers, Reviews, Perspectives and Commentaries, Hypothesis and Meeting Reports. Reviews and Perspectives/Commentaries will typically be invited. We also anticipate to publish special issues that are devoted to rapidly developing or controversial areas of research. Suggestions for topics are welcome. Tissue Barriers objectives: Promote interdisciplinary awareness and collaboration between researchers working with epithelial, epidermal and endothelial barriers and to build a broad and cohesive worldwide community of scientists interesting in this exciting field. Comprehend the enormous complexity of tissue barriers and map cross-talks and interactions between their different cellular and non-cellular components. Highlight the roles of tissue barrier dysfunctions in human diseases. Promote understanding and strategies for restoration of tissue barrier formation and function in regenerative medicine. Accelerate a search for pharmacological enhancers of tissue barriers as potential therapeutic agents. Understand and optimize drug delivery across epithelial and endothelial barriers.
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