利用 Omics 技术识别生命早期的过敏相关生物标志物。

IF 3.3 Q2 ALLERGY
Frontiers in allergy Pub Date : 2024-02-23 eCollection Date: 2024-01-01 DOI:10.3389/falgy.2024.1359142
Elisa Zubeldia-Varela, María Dolores Ibáñez-Sandín, Cristina Gomez-Casado, Marina Pérez-Gordo
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引用次数: 0

摘要

在过去的 30 年里,过敏性疾病的发病率和严重程度都有所上升。了解这些疾病的发病机制是当前过敏学面临的一项重大挑战,因为这对于向精准医学(包括预测、预防和个性化策略)过渡至关重要。在生命的早期阶段确定过敏的预测性生物标志物至关重要,尤其是在食物过敏和特应性皮炎等主要过敏性疾病方面。确定这些生物标志物可以加深我们对未成熟免疫反应的了解,改善早期过敏的处理,并为预防和治疗方法铺平道路。本微综述旨在探讨生命早期三类生物标志物(蛋白质组、微生物组和代谢组)的相关性。首先,在某些过敏性疾病中,一些蛋白质的水平可作为粘膜健康和代谢状态的潜在指标。其次,细菌分类法通过高通量测序方法提供了对微生物群组成的深入了解。最后,代谢物代表细菌和宿主代谢活动的最终产物,是微生物群和宿主代谢变化的早期指标。这些信息有助于广泛鉴定注意力缺失症和注意力缺失症的生物标志物及其在生命早期个性化医学转化中的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Allergy-associated biomarkers in early life identified by Omics techniques.

The prevalence and severity of allergic diseases have increased over the last 30 years. Understanding the mechanisms responsible for these diseases is a major challenge in current allergology, as it is crucial for the transition towards precision medicine, which encompasses predictive, preventive, and personalized strategies. The urge to identify predictive biomarkers of allergy at early stages of life is crucial, especially in the context of major allergic diseases such as food allergy and atopic dermatitis. Identifying these biomarkers could enhance our understanding of the immature immune responses, improve allergy handling at early ages and pave the way for preventive and therapeutic approaches. This minireview aims to explore the relevance of three biomarker categories (proteome, microbiome, and metabolome) in early life. First, levels of some proteins emerge as potential indicators of mucosal health and metabolic status in certain allergic diseases. Second, bacterial taxonomy provides insight into the composition of the microbiota through high-throughput sequencing methods. Finally, metabolites, representing the end products of bacterial and host metabolic activity, serve as early indicators of changes in microbiota and host metabolism. This information could help to develop an extensive identification of biomarkers in AD and FA and their potential in translational personalized medicine in early life.

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CiteScore
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