Shen J, Zheng X, Yan M, Feng M, Ding C, Xie S, Xu H. J Inflamm Res. 2025;18:6191-6202
https://doi.org/10.2147/JIR.S519126
Purpose: Seasonal allergic rhinitis (SAR) is a prevalent inflammatory condition, yet its molecular mechanisms and reliable biomarkers remain incompletely understood. This study aimed to identify key inflammation-related proteins and pathways associated with SAR by investigating seasonal proteomic profile variations and their correlations with SAR symptoms.Graphical Abstract
Patients and Methods: Serum samples were collected from nineteen SAR patients during both allergy (in-season, IS) and non-allergy (out-of-season, OS) periods. Differentially expressed proteins (DEPs) were identified using the Olink Target 96 Inflammation panel, which were further analyzed through Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway enrichment analyses.
Results: A total of 36 inflammation-related DEPs were identified, all significantly upregulated in the allergy season. Notable proteins such as glial cell line-derived neurotrophic factor (GDNF), interleukin-18 receptor 1 (IL-18R1), and interleukin-15 receptor alpha (IL-15RA) showed strong correlations with SAR symptoms. Sneezing was associated with IL-2 receptor beta (IL-2RB) (r = 0.415, p = 0.013), rhinorrhea with FMS-related tyrosine kinase 3 ligand (Flt3L) (r = 0.455, p = 0.004), and nasal blockage with osteoprotegerin (OPG) (r = 0.493, p = 0.002). GO analysis revealed enrichments in Ras signaling and small GTPase pathways, while KEGG analysis highlighted immune-related pathways, including PI3K-Akt signaling and cytokine-cytokine receptor interactions.
Conclusion: This study identified key inflammation-related proteins and pathways that vary seasonally in SAR, offering insights into potential biomarkers and therapeutic targets for SAR management. Further studies are recommended to validate these findings in larger and more diverse populations.

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