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Naslov:Exhausted natural killer cells in adult IgA vasculitis
Avtorji:ID Bajželj, Matija (Avtor)
ID Senjor, Emanuela (Avtor)
ID Boštic, Nika (Avtor)
ID Hladnik, Matjaž (Avtor)
ID Sodin-Šemrl, Snežna (Avtor)
ID Perišić, Milica (Avtor)
ID Kos, Janko (Avtor)
ID Ihan, Alojz (Avtor)
ID Hočevar, Alojzija (Avtor)
ID Kopitar, Andreja Nataša (Avtor)
ID Lakota, Katja (Avtor)
Datoteke:.pdf PDF - Predstavitvena datoteka, prenos (1,65 MB)
MD5: CA60B2DBCA487895C21272AF43E42BFF
 
URL URL - Izvorni URL, za dostop obiščite https://arthritis-research.biomedcentral.com/articles/10.1186/s13075-025-03559-y
 
Jezik:Angleški jezik
Tipologija:1.01 - Izvirni znanstveni članek
Organizacija:Logo UKC LJ - Univerzitetni klinični center Ljubljana
Povzetek: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.
Ključne besede:immunoglobulin A, IgAVN, IgA vasculitis, RNA sequencing, kidney diseases, immunoglobulins, killer cells, adults
Status publikacije:Objavljeno
Verzija publikacije:Objavljena publikacija
Leto izida:2025
Št. strani:str. 1-13
Številčenje:Vol. 27, article no. 95
PID:20.500.12556/DiRROS-24106 Novo okno
UDK:616-097
ISSN pri članku:1478-6362
DOI:10.1186/s13075-025-03559-y Novo okno
COBISS.SI-ID:236303107 Novo okno
Opomba:Nasl. z nasl. zaslona; Opis vira z dne 19. 5. 2025;
Datum objave v DiRROS:12.11.2025
Število ogledov:171
Število prenosov:68
Metapodatki:XML DC-XML DC-RDF
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Gradivo je del revije

Naslov:Arthritis research & therapy
Skrajšan naslov:Arthritis Res Ther
Založnik:BioMed Central.
ISSN:1478-6362
COBISS.SI-ID:3271700 Novo okno

Gradivo je financirano iz projekta

Financer:ARIS - Javna agencija za znanstvenoraziskovalno in inovacijsko dejavnost Republike Slovenije
Številka projekta:P3-0314-2022
Naslov:Sistemske avtoimunske bolezni

Financer:ARIS - Javna agencija za znanstvenoraziskovalno in inovacijsko dejavnost Republike Slovenije
Številka projekta:J7-60132-2025
Naslov:Personalizirana medicina vaskulitisa IgA

Licence

Licenca:CC BY 4.0, Creative Commons Priznanje avtorstva 4.0 Mednarodna
Povezava:http://creativecommons.org/licenses/by/4.0/deed.sl
Opis:To je standardna licenca Creative Commons, ki daje uporabnikom največ možnosti za nadaljnjo uporabo dela, pri čemer morajo navesti avtorja.

Sekundarni jezik

Jezik:Slovenski jezik
Ključne besede:imunoglobulin A, IgAVN, vaskulitis IgA, sekvenciranje RNK, ledvične bolezni, immunoglobulini, celice ubijalke, odrasli


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