Source:http://linkedlifedata.com/resource/pubmed/id/17513755
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
11
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pubmed:dateCreated |
2007-5-21
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pubmed:abstractText |
Activation of Th2 CD4(+) T cells is necessary and sufficient to elicit allergic airway disease, a mouse model with many features of human allergic asthma. Effectively controlling the activities of these cells could be a panacea for asthma therapy. Blood-feeding parasites have devised remarkable strategies to effectively evade the immune response. For example, ticks such as Ixodes scapularis, which must remain on the host for up to 7 days to feed to repletion, secrete immunosuppressive proteins. Included among these proteins is the 15-kDa salivary protein Salp15, which inhibits T cell activation and IL-2 production. Our objective for these studies was to evaluate the T cell inhibitory properties of Salp15 in a mouse model of allergic asthma. BALB/cJ mice were Ag sensitized by i.p. injection of OVA in aluminum hydroxide, with or without 50 mug of Salp15, on days 0 and 7. All mice were challenged with aerosolized OVA on days 14-16 and were studied on day 18. Compared with control mice sensitized with Ag, mice sensitized with Ag and Salp15 displayed significantly reduced airway hyperresponsiveness, eosinophilia, Ag-specific IgG1 and IgE, mucus cell metaplasia, and Th2 cytokine secretion in vivo and by CD4(+) T cells restimulated with Ag in vitro. Our results demonstrate that Salp15 can effectively prevent the generation of a Th2 immune response and the development of experimental asthma. These studies, and those of others, support the notion that a lack of ectoparasitism may contribute to the increasing prevalence of allergic asthma.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
AIM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Adjuvants, Immunologic,
http://linkedlifedata.com/resource/pubmed/chemical/Inflammation Mediators,
http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-13,
http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-4,
http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-5,
http://linkedlifedata.com/resource/pubmed/chemical/Salivary Proteins and Peptides,
http://linkedlifedata.com/resource/pubmed/chemical/Salp15 protein, Ixodes scapularis
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pubmed:status |
MEDLINE
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pubmed:month |
Jun
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pubmed:issn |
0022-1767
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
1
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pubmed:volume |
178
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
7064-71
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pubmed:dateRevised |
2011-5-5
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pubmed:meshHeading |
pubmed-meshheading:17513755-Adjuvants, Immunologic,
pubmed-meshheading:17513755-Animals,
pubmed-meshheading:17513755-Asthma,
pubmed-meshheading:17513755-Bronchial Hyperreactivity,
pubmed-meshheading:17513755-CD4-Positive T-Lymphocytes,
pubmed-meshheading:17513755-Disease Models, Animal,
pubmed-meshheading:17513755-Female,
pubmed-meshheading:17513755-Inflammation Mediators,
pubmed-meshheading:17513755-Interleukin-13,
pubmed-meshheading:17513755-Interleukin-4,
pubmed-meshheading:17513755-Interleukin-5,
pubmed-meshheading:17513755-Ixodes,
pubmed-meshheading:17513755-Mice,
pubmed-meshheading:17513755-Mice, Inbred BALB C,
pubmed-meshheading:17513755-Mucus,
pubmed-meshheading:17513755-Salivary Proteins and Peptides
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pubmed:year |
2007
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pubmed:articleTitle |
The tick salivary protein, Salp15, inhibits the development of experimental asthma.
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pubmed:affiliation |
Department of Medicine, Vermont Lung Center and University of Vermont, Burlington, VT 05405, USA.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't,
Research Support, N.I.H., Extramural
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