Epithelial barrier dysfunction and microbial dysbiosis: exploring the pathogenesis and therapeutic strategies for Crohn's disease.

IF 3.6 Q2 MEDICINE, RESEARCH & EXPERIMENTAL
Tunç Akkoç
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引用次数: 0

Abstract

Crohn's disease (CD), a chronic gastrointestinal inflammatory disease, is becoming more widespread worldwide. Crohn's disease is caused by gut microbiota changes, genetics, environmental stresses, and immunological responses. Current treatments attempt to achieve long-term remission and avoid complications, delaying disease progression. Immunosuppressive measures and combination medicines should be started early for high-risk patients. These medicines monitor inflammatory indicators and adjust as needed. The epithelial barrier helps defend against physical, chemical, and immunological threats. When tissues' protective barrier breaks down, the microbiome may reach the layer underneath. Unbalanced microbial populations and inflammation impair healing and adjustment. Inflammatory cells infiltrating sensitive tissues aggravate the damage and inflammation. This approach promotes chronic inflammatory diseases. The epithelial barrier hypothesis states that hereditary and environmental variables cause epithelial tissue inflammation. This review focuses on how epithelial barrier break-down and microbial dysbiosis cause Crohn's disease and current advances in understanding the epithelial barrier, immune system, and microbiome. Additionally, investigate treatments that restore barrier integrity and promote microbial balance. Overall, it stresses the role of epithelial barrier failure and microbial dysbiosis in Crohn's disease development and discusses current advances in understanding the barrier, immunological responses, and microbiota.

上皮屏障功能障碍和微生物菌群失调:探索克罗恩病的发病机制和治疗策略。
克罗恩病(Crohn's disease,CD)是一种慢性胃肠道炎症性疾病,在全球范围内越来越普遍。克罗恩病是由肠道微生物群变化、遗传、环境压力和免疫反应引起的。目前的治疗方法试图实现长期缓解,避免并发症,延缓疾病进展。对于高危患者,应尽早开始免疫抑制措施和联合用药。这些药物可监测炎症指标,并根据需要进行调整。上皮屏障有助于抵御物理、化学和免疫威胁。当组织的保护屏障破裂时,微生物群可能会到达下层。不平衡的微生物群和炎症会影响愈合和调整。渗入敏感组织的炎症细胞会加剧损伤和炎症。这种方法会助长慢性炎症性疾病。上皮屏障假说认为,遗传和环境变量会导致上皮组织炎症。本综述重点介绍上皮屏障破坏和微生物菌群失调如何导致克罗恩病,以及目前在了解上皮屏障、免疫系统和微生物组方面取得的进展。此外,还探讨了恢复屏障完整性和促进微生物平衡的治疗方法。总之,该书强调了上皮屏障失效和微生物菌群失调在克罗恩病发病中的作用,并讨论了目前在了解屏障、免疫反应和微生物群方面的进展。
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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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