Suppr超能文献

TSLP和IL-1β及其基因变异在儿童单发性和多发性特应性疾病发病机制中的作用。

The Role of TSLP and IL-1 β and Their Genetic Variants in the Pathogenesis of Single and Multiple Atopic Diseases in Children.

作者信息

Sikorska-Szaflik Hanna, Dębińska Anna, Połomska Joanna, Drabik-Chamerska Anna, Sozańska Barbara

机构信息

Department and Clinic of Paediatrics, Allergology and Cardiology, Wroclaw Medical University, ul. Chałubińskiego 2a, 50-368 Wrocław, Poland.

出版信息

J Clin Med. 2025 Jan 17;14(2):598. doi: 10.3390/jcm14020598.

Abstract

Allergic diseases commonly coexist, manifesting in a sequence described as the "allergic march". This study aimed to evaluate TSLP's and IL-1β's potential as biomarkers in both single and multi-pediatric atopic diseases like atopic eczema, food allergy, and anaphylaxis and analyze specific SNPs in the TSLP and IL-1β genes to determine their associations with their occurrence and severity. This analysis included 109 atopic children diagnosed with atopic dermatitis, food allergy, or anaphylaxis alongside a control group of 57 non-atopic children. Recruitment was facilitated through the use of a comprehensive questionnaire. For the study population, the allergen profile was characterized at the molecular level by measuring specific IgE to purified natural or recombinant allergens, assessing serum levels of circulating TSLP and IL-1β, and identifying single-nucleotide polymorphisms in TSLP (rs2289277) and IL-1β (rs16944 C-511T). The serum levels of TSLP and IL-1β were elevated in the study groups compared to the control group, highlighting their significance in the pathogenesis of the studied diseases. Carrying a higher number of the risk allele [C] in the TSLP SNP rs2289277 is associated with the greatest likelihood of having multiple concurrent allergic conditions, with the highest risk observed in individuals with all three conditions-atopic dermatitis, food allergy, and anaphylaxis, simultaneously. Moreover, children carrying the risk allele had a twofold increased risk of polysensitization, which rose to sixfold in those with two copies of the risk allele. Although no significant variations in genotype frequencies were detected for IL-1β rs16944, significant associations were observed for TSLP rs2289277, particularly with conditions such as atopic dermatitis, food allergy, anaphylaxis, and combinations of these diseases. Further research is required to elucidate these pathways and their role in the development of allergic diseases.

摘要

过敏性疾病常并存,表现为一种被称为“过敏进程”的顺序。本研究旨在评估TSLP和IL-1β作为单一和多种儿童特应性疾病(如特应性皮炎、食物过敏和过敏反应)生物标志物的潜力,并分析TSLP和IL-1β基因中的特定单核苷酸多态性(SNP),以确定它们与疾病发生和严重程度的关联。该分析纳入了109名被诊断为特应性皮炎、食物过敏或过敏反应的特应性儿童以及57名非特应性儿童作为对照组。通过使用综合问卷促进了招募工作。对于研究人群,通过测量针对纯化的天然或重组过敏原的特异性IgE、评估循环TSLP和IL-1β的血清水平以及鉴定TSLP(rs2289277)和IL-1β(rs16944 C-511T)中的单核苷酸多态性,在分子水平上对过敏原谱进行了表征。与对照组相比,研究组中TSLP和IL-1β的血清水平升高,突出了它们在研究疾病发病机制中的重要性。在TSLP SNP rs2289277中携带较高数量的风险等位基因[C]与同时患有多种过敏性疾病的最大可能性相关,在同时患有特应性皮炎、食物过敏和过敏反应这三种疾病的个体中观察到的风险最高。此外,携带风险等位基因的儿童发生多敏化的风险增加了两倍,在携带两个拷贝风险等位基因的儿童中则增加到六倍。尽管未检测到IL-1β rs16944基因型频率的显著差异,但观察到TSLP rs2289277存在显著关联,特别是与特应性皮炎、食物过敏、过敏反应以及这些疾病的组合等情况相关。需要进一步研究以阐明这些途径及其在过敏性疾病发展中的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e890/11765508/16a56bab4856/jcm-14-00598-g001.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验