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Title:Exhausted natural killer cells in adult IgA vasculitis
Authors:ID Bajželj, Matija (Author)
ID Senjor, Emanuela (Author)
ID Boštic, Nika (Author)
ID Hladnik, Matjaž (Author)
ID Sodin-Šemrl, Snežna (Author)
ID Perišić, Milica (Author)
ID Kos, Janko (Author)
ID Ihan, Alojz (Author)
ID Hočevar, Alojzija (Author)
ID Kopitar, Andreja Nataša (Author)
ID Lakota, Katja (Author)
Files:.pdf PDF - Presentation file, download (1,65 MB)
MD5: CA60B2DBCA487895C21272AF43E42BFF
 
URL URL - Source URL, visit https://arthritis-research.biomedcentral.com/articles/10.1186/s13075-025-03559-y
 
Language:English
Typology:1.01 - Original Scientific Article
Organization:Logo UKC LJ - Ljubljana University Medical Centre
Abstract:Introduction. IgA vasculitis nephritis (IgAVN) manifests in up to 84% of adult patients with IgA vasculitis (IgAV) and is associated with an elevated risk of progression to chronic kidney failure. The underlying pathogenic mechanism of adult IgAVN in leukocytes remain largely uncharacterised. Although natural killer (NK) cells were investigated in paediatric IgAV, their specific role in the pathogenesis of adult IgAV has yet to be elucidated. Methods. RNA sequencing of leukocytes from adult IgAV patients and healthy controls (HC) was performed. NK cells’ cytotoxicity was assessed using calcein-AM stained K562 cells, and exocytosis was measured by LAMP-1/CD107a expression. Intracellular perforin and granzyme B were analyzed via flow cytometry, and cytokine secretion was measured by Luminex xMAP. Interferon-induced genes were validated with qPCR. Results. Principal component analysis (PCA) of leukocyte gene expression profiles distinguished IgAV patients from HC. Pathway enrichment analysis showed differences in patients’ subsets - Interferon signalling Reactome pathway was observed only in sample from patients with skin-limited IgAV (sl-IgAV) and was confirmed by increased expression of interferon-induced genes using qPCR. Only in samples from IgAVN patients enrichment of NK cell-mediated cytotoxicity KEGG pathway was found. NK cells from IgAVN patients showed significantly decreased cytotoxicity compared to samples from sl-IgAV patients (p = 2.53 × 10− 2). The % of CD107a+-NK cells significantly increased after stimulation in HC (p = 9.7 × 10− 3) and in sl-IgAV patient samples (p = 2.21 × 10− 2) while only a minor increase was observed in samples of IgAVN patients. IgAVN patients exhibited a decreased % of perforin+ NK cells compared to HC. Following phytohemagglutinin (PHA)/interleukin (IL)-2 stimulation, a significant reduction in intracellular perforin level was observed in HC (p = 2.53 × 10− 2), but not in IgAVN patients NK cells. Interferon (IFN)-ϒ and macrophage inflammatory protein (MIP)-1β were significantly decreased in NK cell culture supernatants from IgAVN patients (p = 2.64 × 10− 2 and p = 2.65 × 10− 2 respectively). Conclusion. Patients with IgAVN exhibited impaired cytotoxic and immunomodulatory functions of NK cells, along with a marked absence of interferon signaling in PBMCs. Further studies are needed to confirm if discrimination of patient subsets based on leukocyte samples might be of clinical use and if deregulated NK function might contribute to the pathogenesis of nephritis in adult IgAV.
Keywords:immunoglobulin A, IgAVN, IgA vasculitis, RNA sequencing, kidney diseases, immunoglobulins, killer cells, adults
Publication status:Published
Publication version:Version of Record
Year of publishing:2025
Number of pages:str. 1-13
Numbering:Vol. 27, article no. 95
PID:20.500.12556/DiRROS-24106 New window
UDC:616-097
ISSN on article:1478-6362
DOI:10.1186/s13075-025-03559-y New window
COBISS.SI-ID:236303107 New window
Note:Nasl. z nasl. zaslona; Opis vira z dne 19. 5. 2025;
Publication date in DiRROS:12.11.2025
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Downloads:69
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Record is a part of a journal

Title:Arthritis research & therapy
Shortened title:Arthritis Res Ther
Publisher:BioMed Central.
ISSN:1478-6362
COBISS.SI-ID:3271700 New window

Document is financed by a project

Funder:ARIS - Slovenian Research and Innovation Agency
Project number:P3-0314-2022
Name:Sistemske avtoimunske bolezni

Funder:ARIS - Slovenian Research and Innovation Agency
Project number:J7-60132-2025
Name:Personalizirana medicina vaskulitisa IgA

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.

Secondary language

Language:Slovenian
Keywords:imunoglobulin A, IgAVN, vaskulitis IgA, sekvenciranje RNK, ledvične bolezni, immunoglobulini, celice ubijalke, odrasli


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