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LIBRIS Formathandbok  (Information om MARC21)
FältnamnIndikatorerMetadata
00003897naa a2200481 4500
001oai:DiVA.org:uu-107272
003SwePub
008090803s2010 | |||||||||||000 ||eng|
009oai:prod.swepub.kib.ki.se:120918534
024a https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-1072722 URI
024a https://doi.org/10.1002/art.274172 DOI
024a http://kipublications.ki.se/Default.aspx?queryparsed=id:1209185342 URI
040 a (SwePub)uud (SwePub)ki
041 a engb eng
042 9 SwePub
072 7a ref2 swepub-contenttype
072 7a art2 swepub-publicationtype
100a Kristjánsdóttir, Helga,d 1966-u Uppsala universitet,Medicinsk genetik,Genetics of inflammatory diseases4 aut0 (Swepub:uu)helkr245
2451 0a Lower expression levels of the programmed death 1 receptor on CD4+CD25+ T cells and correlation with the PD-1.3A genotype in patients with systemic lupus erythematosus
264 c 2010-02-22
264 1b Wiley,c 2010
338 a print2 rdacarrier
520 a OBJECTIVE.: A genetic polymorphism, PD1.3A, in the PDCD1 gene encoding the co-inhibitory immunoreceptor PD-1, has been associated with SLE. The aim of the study was to assess PD-1 receptor expression in SLE patients, relatives and controls and correlate with PD-1.3A. METHODS.: Icelandic and Swedish SLE patients, relatives and controls were studied. PBMCs were stimulated with alphaCD3/CD28 and PD-1 expression analyzed by flow cytometry. PD-1.3A/G genotyping was performed by PCR-RFLP. RESULTS: I. PD-1 expression on PBMCs was induced after stimulation, by 2.1-fold in SLE patients, 3.1-fold in relatives and 5.1-fold in controls.II. The frequency of PD-1+ cells was significantly lower in SLE patients compared to relatives and controls. PD-1 expression on PD-1+ cells was significantly lower in SLE patients and relatives.III. PD-1 expression on CD4+CD25+ T cells was significantly lower in SLE patients and relatives.IV. PD-1 expression was significantly higher on CD25(high) compared to CD25(intermediate) and (low) cells.V. PD-1 expression on CD25(high) and CD25(intermediate) cells was significantly lower in SLE patients compared to controls.VI. PD-1 was expressed on both FoxP3- and FoxP3+ cells.VII. Lower PD-1 expression was significantly correlated with the PD-1.3A/G genotype. CONCLUSION.: The study demonstrates significantly lower PD-1 receptor expression in SLE patients and relatives and a significant correlation of lower PD-1 expression with the PD-1.3A allele. We conclude that PD-1.3A may be contributory to abnormalities in PD-1 receptor expression on CD4+CD25+ T-cells in SLE, providing support for an important role for the PD-1 pathway in SLE and possibly other autoimmune diseases.
650 7a MEDICIN OCH HÄLSOVETENSKAPx Medicinska och farmaceutiska grundvetenskaperx Immunologi inom det medicinska området0 (SwePub)301102 hsv//swe
650 7a MEDICAL AND HEALTH SCIENCESx Basic Medicinex Immunology in the medical area0 (SwePub)301102 hsv//eng
653 a SLE
653 a PD-1.3A
653 a self-tolerance
653 a Immunology
653 a Immunologi
653 a Immunologi
653 a Immunology
700a Steinsson, Kristjan4 aut
700a Gunnarsson, Ivau Karolinska Institutet4 aut
700a Gröndal, Gerdur4 aut
700a Erlendsson, Kristjan4 aut
700a Alarcón-Riquelme, Marta E.u Uppsala universitet,Medicinsk genetik4 aut
710a Uppsala universitetb Medicinsk genetik4 org
773t Arthritis and Rheumatismd : Wileyg 62:6, s. 1702-1711q 62:6<1702-1711x 0004-3591x 1529-0131
856u https://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/art.27417
8564 8u https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-107272
8564 8u https://doi.org/10.1002/art.27417
8564 8u http://kipublications.ki.se/Default.aspx?queryparsed=id:120918534

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