Source:http://linkedlifedata.com/resource/pubmed/id/12702146
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rdf:type | |
lifeskim:mentions |
umls-concept:C0010453,
umls-concept:C0017262,
umls-concept:C0021758,
umls-concept:C0039194,
umls-concept:C0185117,
umls-concept:C0221198,
umls-concept:C0221928,
umls-concept:C0442805,
umls-concept:C0444498,
umls-concept:C0547047,
umls-concept:C1123023,
umls-concept:C1441547,
umls-concept:C1522449,
umls-concept:C2911684
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pubmed:issue |
2
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pubmed:dateCreated |
2003-4-18
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pubmed:abstractText |
Type 1 cytokine producing T cells play an important role in the pathogenesis of psoriasis. Ultraviolet-B (UVB) irradiation is effective in the treatment of this disease. In normal skin, UVB causes a change in dermal microenvironment, leading to a decrease of IFN-gamma expressing type 1 T cells and a concurrent increase of IL-4 expressing type 2 T cells. The aim of this study was to show whether UVB irradiation causes a like-wise shift of type 1 and type 2 responses in psoriatic skin. For this purpose, biopsies were obtained from the lesional skin of psoriatic patients before, 2 days and 14 days after a single exposure to 4 MED UVB. Sections from these biopsies were immunostained (CD3, IFN-gamma and IL-4) or RNA was extracted and analyzed for the expressions of IFN-gamma and IL-4 by PCR. In addition, primary cultures of T cells from dermal cell suspensions were stained intracellularly for IFN-gamma and IL-4 expression and CD4+ and CD8+ T subsets were analyzed by flow cytometry. IFN-gamma was abundantly expressed in situ before irradiation and decreased in all patients after UVB irradiation, whereas IL-4 expression was variably expressed before irradiation and increased in different degrees after irradiation. Cytokine mRNA expressions determined by PCR showed a clear decrease of IFN-gamma and increase of IL-4 following UVB irradiation. Both CD4+ and CD8+ dermal T cells were found to produce less IFN-gamma and more IL-4 following UVB irradiation as determined by flow cytometry. Decrease in IFN-gamma expression and increase in IL-4 expression of dermal T cells in psoriatic lesions after UVB irradiation may lead to decrease in local immunoreactivity. These changes could be part of the therapeutic effects of UVB on psoriasis.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Apr
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pubmed:issn |
0906-6705
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
12
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
172-80
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pubmed:dateRevised |
2008-11-21
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pubmed:meshHeading |
pubmed-meshheading:12702146-Base Sequence,
pubmed-meshheading:12702146-Cells, Cultured,
pubmed-meshheading:12702146-Gene Expression,
pubmed-meshheading:12702146-Humans,
pubmed-meshheading:12702146-Immunohistochemistry,
pubmed-meshheading:12702146-Interferon-gamma,
pubmed-meshheading:12702146-Interleukin-4,
pubmed-meshheading:12702146-Psoriasis,
pubmed-meshheading:12702146-RNA, Messenger,
pubmed-meshheading:12702146-Skin,
pubmed-meshheading:12702146-T-Lymphocytes,
pubmed-meshheading:12702146-Ultraviolet Therapy
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pubmed:year |
2003
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pubmed:articleTitle |
Ultraviolet-B irradiation decreases IFN-gamma and increases IL-4 expression in psoriatic lesional skin in situ and in cultured dermal T cells derived from these lesions.
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pubmed:affiliation |
Department of Dermatology, Academic Medical Center Amsterdam, The Netherlands. g.piskin@amc.uva.nl
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pubmed:publicationType |
Journal Article
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