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Title:Cytokine profiles of bronchoalveolar lavage in patients with interstitial lung diseases and non-allergic asthma
Authors:ID Greif Lenarčič, Dana, Univerzitetna klinika za pljučne bolezni in alergijo Golnik (Author)
ID Bidovec, Urška, Univerzitetna klinika za pljučne bolezni in alergijo Golnik (Author)
ID Kristanc, Pia, Univerzitetna klinika za pljučne bolezni in alergijo Golnik (Author)
ID Kopač, Peter, Univerzitetna klinika za pljučne bolezni in alergijo Golnik (Author)
ID Marc-Malovrh, Mateja, Univerzitetna klinika za pljučne bolezni in alergijo Golnik (Author)
ID Kern, Izidor, Univerzitetna klinika za pljučne bolezni in alergijo Golnik (Author)
ID Osolnik, Katarina, Univerzitetna klinika za pljučne bolezni in alergijo Golnik (Author)
ID Korošec, Peter, Univerzitetna klinika za pljučne bolezni in alergijo Golnik (Corresponding author)
Files:URL URL - Source URL, visit https://www.mdpi.com/1422-0067/26/14/6831
 
.pdf PDF - Presentation file, download (1,19 MB)
MD5: 1D62D75A1F7DCBE3EC9EA61191CD4C0F
 
Language:English
Typology:1.01 - Original Scientific Article
Organization:Logo UKPBAG - University Clinic of Respiratory and Allergic Diseases Golnik
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.
Keywords:hypersensitivity pneumonitis, sarcoidosis, non-allergic asthma, amiodarone lung, EGPA, cytokines, bronchoalveolar lavage, chemokines, complement anaphylatoxins, angiogenesis-related factors
Publication status:Published
Publication version:Version of Record
Submitted for review:02.06.2025
Article acceptance date:06.06.2025
Publication date:15.07.2025
Publisher:MDPI, 2000-
Year of publishing:2025
Number of pages:14 str.
Numbering:Vol. 26, issue 14, [article no.] 6831
Source:International journal of molecular sciences
PID:20.500.12556/DiRROS-23211 New window
UDC:616.24-002.2
ISSN on article:1422-0067
DOI:10.3390/ijms26146831 New window
COBISS.SI-ID:244836099 New window
Copyright:© 2025 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
Note:Nasl. z nasl. zaslona; Opis vira z dne 5. 8. 2025;
Publication date in DiRROS:05.08.2025
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Downloads:253
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Record is a part of a journal

Title:International journal of molecular sciences
Shortened title:Int. j. mol. sci.
Publisher:MDPI
ISSN:1422-0067
COBISS.SI-ID:2779162 New window

Document is financed by a project

Funder:ARIS - Slovenian Research and Innovation Agency
Project number:P3-0360
Name:Celostna obravnava alergijskih bolezni in astme v Sloveniji: od epidemiologije do genetike

Funder:ARIS - Slovenian Research and Innovation Agency
Funding programme:J3–50099
Project number:J3-50099
Name:Nov terapevtski pristop za zdravljenje alergijskih bolezni, ki temelji na inhibiciji interakcije med epitopi in paratopi

Licences

License:CC BY 4.0, Creative Commons Attribution 4.0 International
Link:http://creativecommons.org/licenses/by/4.0/
Description:This is the standard Creative Commons license that gives others maximum freedom to do what they want with the work as long as they credit the author.
Licensing start date:16.07.2025

Secondary language

Language:Slovenian
Keywords:preobčutljivostna pljučnica, sarkoidoza, nealergijska astma, pljučna toksičnost zaradi amiodarona, eozinofilni granulomatozni poliangiitis, citokini, bronhoalveolarno izpiranje, kemokini, komplementni anafilatoksini, dejavniki, povezani z angiogenezo


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