Browne William, Hopkins Georgina, Cochrane Stella, James Victoria, Onion David, Fairclough Lucy C
School of Life Sciences, University of Nottingham, Nottingham NG7 2RD, UK.
Unilever SERS, Colworth Science Park, Sharnbrook MK44 1LQ, UK.
Int J Mol Sci. 2025 Jun 17;26(12):5791. doi: 10.3390/ijms26125791.
The aim of this systematic review was to evaluate the current evidence for the involvement of epithelial-derived extracellular vesicles (EVs) in Immunoglobulin E (IgE)-mediated allergic sensitisation. Original clinical and research studies specifically examining the effect of epithelial-derived EVs in IgE-mediated allergic sensitisation were included. Non-IgE mediated allergies, abstracts and review articles were excluded. A total of 18 publications were identified from three databases (EMBASE, Web of Science and PubMed) that indicate epithelial-derived EVs have the potential to promote tolerance or allergic sensitisation. For example, epithelial-derived EVs have the potential to promote IgE-mediated allergic sensitisation by delivering mRNAs that promote T helper 2 (Th2) polarisation and cytokine secretion, or promote tolerance through the induction of T regulatory (Treg) cells. The results also indicate that the potential role of epithelial-derived EVs in IgE-mediated allergic sensitisation may be dependent on the barrier, with all publications related to intestinal epithelium driving tolerance, but publications on nasal and bronchial/alveolar epithelia gaving mixed effects. No publications were found on cutaneous epithelia. Taken together, the literature suggests that epithelial-derived EVs play a key role in influencing IgE-mediated allergic sensitisation. Further research examining all epithelial barriers, using both robust human in vitro models that give more biologically relevant information, as well as clinical studies, are required to further characterise the role of epithelial-derived EVs in IgE-mediated allergic sensitisation.
本系统评价的目的是评估目前关于上皮来源的细胞外囊泡(EVs)参与免疫球蛋白E(IgE)介导的过敏致敏作用的证据。纳入了专门研究上皮来源的EVs在IgE介导的过敏致敏中作用的原始临床和研究。排除非IgE介导的过敏、摘要和综述文章。从三个数据库(EMBASE、科学网和PubMed)中总共鉴定出18篇出版物,这些出版物表明上皮来源的EVs有促进耐受或过敏致敏的潜力。例如,上皮来源的EVs有通过传递促进辅助性T细胞2(Th2)极化和细胞因子分泌的mRNA来促进IgE介导的过敏致敏的潜力,或者通过诱导调节性T(Treg)细胞来促进耐受。结果还表明,上皮来源的EVs在IgE介导的过敏致敏中的潜在作用可能取决于屏障,所有与肠上皮相关的出版物都促进耐受,但关于鼻和支气管/肺泡上皮的出版物有混合效应。未发现关于皮肤上皮的出版物。综上所述,文献表明上皮来源的EVs在影响IgE介导的过敏致敏中起关键作用。需要进一步开展研究,利用能提供更多生物学相关信息的强大的人体体外模型以及临床研究,来全面研究所有上皮屏障,以进一步明确上皮来源的EVs在IgE介导的过敏致敏中的作用。