Evidence map›Paper›PMID 40725075›Full record

ArticleInternational journal of molecular sciences2025

Cytokine Profiles of Bronchoalveolar Lavage in Patients with Interstitial Lung Diseases and Non-Allergic Asthma.

Dana Greif Lenarčič, Urska Bidovec Stojković, Pia Kristanc, Peter Kopač, Mateja Marc Malovrh, Izidor Kern, Katarina Osolnik, Peter Korošec

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Article in International journal of molecular sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Dana Greif LenarčičUniversity Clinic of Respiratory and Allergic Diseases, 4204 Golnik, Slovenia.
Urska Bidovec StojkovićUniversity Clinic of Respiratory and Allergic Diseases, 4204 Golnik, Slovenia.ORCID 0000-0001-8978-6887
Pia KristancUniversity Clinic of Respiratory and Allergic Diseases, 4204 Golnik, Slovenia.
Peter KopačUniversity Clinic of Respiratory and Allergic Diseases, 4204 Golnik, Slovenia.ORCID 0000-0001-7261-6689
Mateja Marc MalovrhUniversity Clinic of Respiratory and Allergic Diseases, 4204 Golnik, Slovenia.
Izidor KernUniversity Clinic of Respiratory and Allergic Diseases, 4204 Golnik, Slovenia.
Katarina OsolnikUniversity Clinic of Respiratory and Allergic Diseases, 4204 Golnik, Slovenia.
Peter KorošecUniversity Clinic of Respiratory and Allergic Diseases, 4204 Golnik, Slovenia.

Funding

The Slovenian Research and Innovation Agency P3-0360 and J3-50099
6 · The paper itself

Abstract

Diagnosing and prognosing immune-mediated airway diseases, like hypersensitivity pneumonitis (HP) and sarcoidosis, is complicated due to their overlapping symptoms and the lack of definitive biomarkers. Hence, we wanted to compare bronchoalveolar lavage (BAL) cytokine and chemokine profiles from 92 patients with different immune-mediated and inflammatory airway diseases, namely, HP, sarcoidosis, non-allergic asthma, amiodarone lung, and EGPA. We also compared pulmonary function parameters, BAL's cellularity, and lymphocyte immunophenotypes. We found significant differences across all measured lung functions (VC, VC%, FEV1, FEV1%, and Tiff%) and in the number of macrophages, lymphocytes, neutrophils, and eosinophils. Furthermore, we showed significant differences in CD4, CD8, and CD4/8 across all included ILDs and OLDs; however, no significant differences were found in CD3, CD19, NK, or NKT. We identified nine biomarkers (IL-1β, IL-6, IL-8, IL-13, VEGF, angiogenin, C4a, RANTES, and MCP-1) that significantly differ in the BAL of patients with HP and sarcoidosis and showed that RANTES and IL-6 are associated with fibrotic outcome. We have demonstrated that interstitial and obstructive lung diseases differ in cytokine and cellular lung imprint, which may, in the future, enable the determination of the disease subtype and thus the identification of targets for the treatment of individuals or subgroups within diseases.

Indexed as

AsthmaBronchoalveolar Lavage FluidCytokinesLung Diseases, InterstitialAdultAgedBiomarkersFemaleHumansMaleMiddle AgedBiomarkersCytokinesamiodarone lungangiogenesis-related factorsbronchoalveolar lavagechemokinescomplement anaphylatoxinscytokinesEGPAhypersensitivity pneumonitisnon-allergic asthmasarcoidosis

Identifiers

PMID40725075
PMCPMC12295261

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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 OpenQuestion graph.