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LIBRIS Formathandbok  (Information om MARC21)
FältnamnIndikatorerMetadata
00004424naa a2200433 4500
001oai:DiVA.org:liu-79798
003SwePub
008120814s2012 | |||||||||||000 ||eng|
009oai:gup.ub.gu.se/160363
024a https://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-797982 URI
024a https://doi.org/10.1371/journal.pone.00390162 DOI
024a https://gup.ub.gu.se/publication/1603632 URI
040 a (SwePub)liud (SwePub)gu
041 a engb eng
042 9 SwePub
072 7a ref2 swepub-contenttype
072 7a art2 swepub-publicationtype
100a Zhao, Yelinu Linköpings universitet,Institutionen för klinisk och experimentell medicin,Hälsouniversitetet4 aut
2451 0a Combined Multivariate and Pathway Analyses Show That Allergen-Induced Gene Expression Changes in CD4(+) T Cells Are Reversed by Glucocorticoids
264 c 2012-06-12
264 1b Public Library of Science,c 2012
338 a electronic2 rdacarrier
520 a Background: Glucocorticoids (GCs) play a key role in the treatment of allergy. However, the genome-wide effects of GCs on gene expression in allergen-challenged CD4(+) T cells have not been described. The aim of this study was to perform a genome-wide analysis to investigate whether allergen-induced gene expression changes in CD4(+) T cells could be reversed by GCs. Methodology/Principal Findings: Gene expression microarray analysis was performed to profile gene expression in diluent( D), allergen- (A), and allergen + hydrocortisone- (T) challenged CD4(+) T cells from patients with seasonal allergic rhinitis. Principal component analysis (PCA) showed good separation of the three groups. To identify the correlation between changes in gene expression in allergen-challenged CD4(+) T cells before and after GC treatment, we performed orthogonal partial least squares discriminant analysis (OPLS-DA) followed by Pearson correlation analysis. This revealed that allergen-induced genes were widely reversed by GC treatment (r = -0.77, Pless than0.0001). We extracted 547 genes reversed by GC treatment from OPLS-DA models based on their high contribution to the discrimination and found that those genes belonged to several different inflammatory pathways including TNFR2 Signalling, Interferon Signalling, Glucocorticoid Receptor Signalling and T Helper Cell Differentiation. The results were supported by gene expression microarray analyses of two independent materials. Conclusions/Significance: Allergen-induced gene expression changes in CD4(+) T cells were reversed by treatment with glucocorticoids. The top allergen-induced genes that reversed by GC treatment belonged to several inflammatory pathways and genes of known or potential relevance for allergy.
650 7a MEDICIN OCH HÄLSOVETENSKAPx Klinisk medicinx Pediatrik0 (SwePub)302212 hsv//swe
650 7a MEDICAL AND HEALTH SCIENCESx Clinical Medicinex Pediatrics0 (SwePub)302212 hsv//eng
653 a MEDICINE
653 a MEDICIN
700a Wang, Huiu Gothenburg University,Göteborgs universitet,Linköpings universitet,Institutionen för klinisk och experimentell medicin,Hälsouniversitetet,Institutionen för kliniska vetenskaper, Avdelningen för pediatrik,Institute of Clinical Sciences, Department of Pediatrics4 aut0 (Swepub:gu)xwanhu
700a Gustafsson, Mikau Linköpings universitet,Institutionen för klinisk och experimentell medicin,Hälsouniversitetet4 aut0 (Swepub:liu)mikgu75
700a Muraro, Antonellau University of Padua, Italy4 aut
700a Bruhn, Sörenu Linköpings universitet,Institutionen för klinisk och experimentell medicin,Hälsouniversitetet4 aut0 (Swepub:liu)sorbr27
700a Benson, Mikaelu Linköpings universitet,Institutionen för klinisk och experimentell medicin,Hälsouniversitetet4 aut0 (Swepub:gu)xbenmi
710a Linköpings universitetb Institutionen för klinisk och experimentell medicin4 org
773t PLOS ONEd : Public Library of Scienceg 7:6q 7:6x 1932-6203
856u https://liu.diva-portal.org/smash/get/diva2:544985/FULLTEXT01.pdfx primaryx Raw objecty fulltext:print
856u https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0039016&type=printable
8564 8u https://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-79798
8564 8u https://doi.org/10.1371/journal.pone.0039016
8564 8u https://gup.ub.gu.se/publication/160363

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