SwePub
Sök i LIBRIS databas

  Extended search

onr:"swepub:oai:DiVA.org:uu-343246"
 

Search: onr:"swepub:oai:DiVA.org:uu-343246" > EOMES-positive CD4+...

  • 1 of 1
  • Previous record
  • Next record
  •    To hitlist
  • Chemin, KarineKarolinska Institutet (author)

EOMES-positive CD4+ T cells are increased in PTPN22 (1858T) risk allele carriers.

  • Article/chapterEnglish2018

Publisher, publication year, extent ...

  • 2018-02-28
  • Wiley,2018
  • printrdacarrier

Numbers

  • LIBRIS-ID:oai:DiVA.org:uu-343246
  • https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-343246URI
  • https://doi.org/10.1002/eji.201747296DOI
  • http://kipublications.ki.se/Default.aspx?queryparsed=id:138038104URI

Supplementary language notes

  • Language:English
  • Summary in:English

Part of subdatabase

Classification

  • Subject category:ref swepub-contenttype
  • Subject category:art swepub-publicationtype

Notes

  • The presence of the PTPN22 risk allele (1858T) is associated with several autoimmune diseases including rheumatoid arthritis (RA). Despite a number of studies exploring the function of PTPN22 in T cells, the exact impact of the PTPN22 risk allele on T-cell function in humans is still unclear. In this study, using RNA sequencing, we show that, upon TCR-activation, naïve human CD4+ T cells homozygous for the PTPN22 risk allele overexpress a set of genes including CFLAR and 4-1BB, which are important for cytotoxic T-cell differentiation. Moreover, the protein expression of the T-box transcription factor Eomesodermin (EOMES) was increased in T cells from healthy donors homozygous for the PTPN22 risk allele and correlated with a decreased number of naïve CD4+ T cells. There was no difference in the frequency of other CD4+ T cell subsets (Th1, Th17, Tfh, Treg). Finally, an accumulation of EOMES+CD4+ T cells was observed in synovial fluid of RA patients with a more pronounced production of Perforin-1 in PTPN22 risk allele carriers. Altogether, we propose a novel mechanism of action of PTPN22 risk allele through the generation of cytotoxic CD4+ T cells and identify EOMES+CD4+ T cells as a relevant T-cell subset in RA pathogenesis.

Subject headings and genre

Added entries (persons, corporate bodies, meetings, titles ...)

  • Ramsköld, DanielKarolinska Institutet (author)
  • Diaz-Gallo, Lina-MarcelaKarolinska Institutet (author)
  • Herrath, JessicaRheumatology Unit, Department of Medicine, Karolinska University Hospital Solna, Karolinska Institute, Stockholm, Sweden (author)
  • Houtman, MirandaKarolinska Institutet (author)
  • Tandre, KarolinaUppsala universitet,Reumatologi,Science for Life Laboratory, SciLifeLab(Swepub:uu)karotand (author)
  • Rönnblom, LarsUppsala universitet,Reumatologi,Science for Life Laboratory, SciLifeLab(Swepub:uu)larsronn (author)
  • Catrina, AncaKarolinska Institutet (author)
  • Malmström, VivianneKarolinska Institutet (author)
  • Karolinska InstitutetRheumatology Unit, Department of Medicine, Karolinska University Hospital Solna, Karolinska Institute, Stockholm, Sweden (creator_code:org_t)

Related titles

  • In:European Journal of Immunology: Wiley48:4, s. 655-6690014-29801521-4141

Internet link

Find in a library

To the university's database

  • 1 of 1
  • Previous record
  • Next record
  •    To hitlist

Kungliga biblioteket hanterar dina personuppgifter i enlighet med EU:s dataskyddsförordning (2018), GDPR. Läs mer om hur det funkar här.
Så här hanterar KB dina uppgifter vid användning av denna tjänst.

 
pil uppåt Close

Copy and save the link in order to return to this view