Evidence map›Paper›PMID 40132576›Full record

ArticleInternational archives of allergy and immunology2025

MicroRNA-4497 Is Downregulated in Pediatric Allergic Diseases and Suppresses Th2 Inflammation in an Animal Model.

Young Yoo, Jue Seong Lee, Yongsung Park, Changhak Han, Seunghyun Kim, Wonsuck Yoon, Young Yoo

Abstract read
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Article in International archives of allergy and immunology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

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2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Young Yoo
Jue Seong LeeDepartment of Pediatrics, Korea University College of Medicine, Seoul, Republic of Korea.
Yongsung ParkAllergy Immunology Center, Korea University, Seoul, Republic of Korea.
Changhak HanAllergy Immunology Center, Korea University, Seoul, Republic of Korea.
Seunghyun KimAllergy Immunology Center, Korea University, Seoul, Republic of Korea.
Wonsuck YoonAllergy Immunology Center, Korea University, Seoul, Republic of Korea.
Young YooDepartment of Pediatrics, Korea University College of Medicine, Seoul, Republic of Korea.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

<p>Introduction: Atopic dermatitis (AD), allergic rhinitis (AR), and bronchial asthma (BA) are major allergic diseases in childhood. Pediatric allergic diseases are characterized by the "atopic march," where two or more allergic conditions can occur either simultaneously or sequentially. MicroRNAs (miRNAs) serve as fine regulators of gene expression, capable of modulating the clinical manifestations of allergic diseases posttranscriptionally. We investigated miRNAs commonly expressed in these three allergic diseases to enhance the understanding of their development and management.

methodsWe collected serum samples from subjects diagnosed with AD, AR, and BA as well as from healthy controls at Korea University Anam Hospital. Their miRNA expression patterns were analyzed using microarray technology. Additionally, we examined the allergic inflammatory response of miRNA through an allergic animal model.

resultsA total of 68 subjects were enrolled in the allergy group, consisting of 42 with AD, 13 with AR, and 13 with BA, while 10 children participated as controls. Microarray analysis revealed that miR-4497 expression levels were consistently downregulated in these three allergic disease groups. Following mast cell activation and miR-4497 transfection, reduced levels of macrophage-derived chemokines (MDCs) were observed. Furthermore, levels of IL-4, MDC, and methacholine Penh were significantly decreased in a miR-4497-treated mouse model.

conclusionsMiR-4497 expressions were consistently downregulated in pediatric subjects with AD, AR, and BA. Allergic inflammation was significantly reduced in human mast cell-1 transfected with miR-4497 and in the treated mouse model. Further research is needed to elucidate the epigenetic mechanisms by which miR-4497 modulates allergic diseases and to explore its potential as a noninvasive biomarker for diagnosis and treatment. </p>.

Indexed as

AsthmaDermatitis, AtopicHypersensitivityMicroRNAsTh2 CellsAdolescentAnimalsChildChild, PreschoolDisease Models, AnimalDown-RegulationFemaleHumansInflammationMaleMast CellsMicroRNAsAllergic diseaseAllergic rhinitisAtopic dermatitisBronchial asthmaMacrophage-derived chemokineMicroarrayMicroRNAMiR-4497

Identifiers

PMID40132576
PMCPMC12064137

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LicenceCC BY-NC
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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.