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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
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pubmed:dateCreated |
1987-10-20
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pubmed:abstractText |
When UVB-irradiated urocanic acid, the putative photoreceptor/mediator for UVB suppression, is administered to mice it induces a dose-dependent suppression of the delayed-type hypersensitivity response to herpes simplex virus, type 1 (HSV-1), of similar magnitude to that induced by UV irradiation of mice. In this study, the efferent suppression of delayed-type hypersensitivity by UV-irradiated urocanic acid is demonstrated to be due to 2 phenotypically distinct T cells, (Thy1+, L3T4-, Ly2+) and (Thy1+, L3T4+, Ly2-). The suppression is specific for HSV-1. This situation parallels the generation of 2 distinct T-suppressor cells for HSV-1 by UV irradiation of mice and provides further evidence for the involvement of urocanic acid in the generation of UVB suppression.
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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 |
Sep
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pubmed:issn |
0022-202X
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
89
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
230-3
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:3040867-Animals,
pubmed-meshheading:3040867-Female,
pubmed-meshheading:3040867-Hypersensitivity, Delayed,
pubmed-meshheading:3040867-Imidazoles,
pubmed-meshheading:3040867-Immune Tolerance,
pubmed-meshheading:3040867-Male,
pubmed-meshheading:3040867-Mice,
pubmed-meshheading:3040867-Phenotype,
pubmed-meshheading:3040867-Simplexvirus,
pubmed-meshheading:3040867-Spleen,
pubmed-meshheading:3040867-T-Lymphocytes,
pubmed-meshheading:3040867-T-Lymphocytes, Regulatory,
pubmed-meshheading:3040867-Ultraviolet Rays,
pubmed-meshheading:3040867-Urocanic Acid
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pubmed:year |
1987
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pubmed:articleTitle |
Two phenotypically distinct T cells are involved in ultraviolet-irradiated urocanic acid-induced suppression of the efferent delayed-type hypersensitivity response to herpes simplex virus, type 1 in vivo.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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