Hyppää sisältöön
    • Suomeksi
    • In English
Trepo
  • Suomeksi
  • In English
  • Kirjaudu
Näytä viite 
  •   Etusivu
  • Trepo
  • TUNICRIS-julkaisut
  • Näytä viite
  •   Etusivu
  • Trepo
  • TUNICRIS-julkaisut
  • Näytä viite
JavaScript is disabled for your browser. Some features of this site may not work without it.

Autoantibody response towards chromatin in patients with juvenile idiopathic arthritis

Pitkänen, Viola; Remes-Pakarinen, Terhi; Vähäsalo, Paula; Möttönen, Milja; Grönlund, Minna Maija; Arvonen, Miika; Knip, Mikael; Veijola, Riitta; Toppari, Jorma; Ilonen, Jorma; Lempainen, Johanna; Schroderus, Anna Mari; Kröger, Liisa; Kinnunen, Tuure (2025-07-16)

 
Avaa tiedosto
Arthritis_Rheumatology_-_2025_-_Pitk_nen_-_Autoantibody_response_towards_chromatin_in_patients_with_juvenile_idiopathic.pdf (18.79Mt)
Lataukset: 



Pitkänen, Viola
Remes-Pakarinen, Terhi
Vähäsalo, Paula
Möttönen, Milja
Grönlund, Minna Maija
Arvonen, Miika
Knip, Mikael
Veijola, Riitta
Toppari, Jorma
Ilonen, Jorma
Lempainen, Johanna
Schroderus, Anna Mari
Kröger, Liisa
Kinnunen, Tuure
16.07.2025

Arthritis and Rheumatology
doi:10.1002/art.43315
Näytä kaikki kuvailutiedot
Julkaisun pysyvä osoite on
https://urn.fi/URN:NBN:fi:tuni-202509189362

Kuvaus

Peer reviewed
Tiivistelmä
Objective: Juvenile idiopathic arthritis (JIA) patients frequently exhibit antinuclear antibodies (ANAs), but the specific antigen target recognized by them and the presence of additional autoantibody specificities in JIA patients remains elusive. Methods: Plasma samples from 110 untreated patients with active JIA, as well as from 14 children with unspecified arthritis and 151 age- and sex-matched healthy children were analyzed with multiple modern clinical-grade autoantibody assays, including automated indirect immunofluorescence to screen for ANAs with HEp-2 cells, and specific immune assays to detect reactivity to individual autoantigens. In addition, a HuProt proteome microarray was used to screen for novel autoantibody targets in plasma samples from five ANA-positive JIA patients and four ANA-negative healthy controls. Results: Homogeneous nuclear ANA staining, indicating reactivity towards chromatin, was detected in most (61.8%) JIA patients but rarely in healthy controls (2.7%; p<0.0001). No antibody reactivity to specific nuclear antigens or other autoantigens associated with connective tissue diseases was detected. However, 20% of JIA patients harbored antibodies against dsDNA-nucleosome complexes (compared to 2.7% of controls, p<0.0001). Finally, the proteome microarray revealed core histone H2A variant H2AFY, part of the nucleosome, to be the most widely recognized human protein by autoantibodies of JIA patients. Conclusion: Autoantibody reactivity in JIA primarily targets chromatin, but the epitopes targeted are likely either posttranslationally modified or multi-molecule epitopes, such as dsDNA-nucleosome complexes, rather than epitopes on individual native proteins or purified dsDNA.
Kokoelmat
  • TUNICRIS-julkaisut [22206]
Kalevantie 5
PL 617
33014 Tampereen yliopisto
oa[@]tuni.fi | Tietosuoja | Saavutettavuusseloste
 

 

Selaa kokoelmaa

TekijätNimekkeetTiedekunta (2019 -)Tiedekunta (- 2018)Tutkinto-ohjelmat ja opintosuunnatAvainsanatJulkaisuajatKokoelmat

Omat tiedot

Kirjaudu sisäänRekisteröidy
Kalevantie 5
PL 617
33014 Tampereen yliopisto
oa[@]tuni.fi | Tietosuoja | Saavutettavuusseloste