Source:http://linkedlifedata.com/resource/pubmed/id/11828375
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rdf:type | |
lifeskim:mentions |
umls-concept:C0002092,
umls-concept:C0003261,
umls-concept:C0015219,
umls-concept:C0020846,
umls-concept:C0020852,
umls-concept:C0020861,
umls-concept:C0181904,
umls-concept:C0441712,
umls-concept:C0449432,
umls-concept:C0456387,
umls-concept:C0596972,
umls-concept:C0599196,
umls-concept:C0728873,
umls-concept:C1179435,
umls-concept:C1521743,
umls-concept:C1524073,
umls-concept:C1548799,
umls-concept:C1704646,
umls-concept:C1705248,
umls-concept:C1707719
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pubmed:issue |
2
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pubmed:dateCreated |
2002-2-5
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pubmed:abstractText |
The formation of IgE antibodies against environmental allergens represents the hallmark of type I allergy. Data from in vitro cultured cells and experimental animal models provide controversial evidence for isotype switching from IgM to IgE production via sequential as well as non-sequential (i.e. direct) class switch. We analyzed the evolution of IgE responses in 11 children developing birch pollen and/or grass pollen allergy during the first 7 years of life using purified recombinant allergen molecules (major birch pollen allergen, Bet v 1; major timothy grass pollen allergens, Phl p 1, Phl p 2, Phl p 5). Demographic, clinical and serological data indicated a postnatal sensitization to pollen allergens. A parallel development of IgG(1-4) and IgE responses to recombinant allergen molecules compatible with a strictly sequential class switch to IgE was observed only in one child. The only partly synchronized and dissociated development of allergen-specific antibody responses found in all other cases can be best explained by a partly sequential class switch involving few switch stations or, more likely, by direct class switching. Kinetics and courses of allergen-specific antibody responses (IgM, IgG(1-4), IgE) during the first years of life suggest that, once established, allergen-specific IgE responses are driven by antigen contact rather than by cytokines controlling class switch to IgE.
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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 |
Feb
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pubmed:issn |
0014-2980
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
32
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
576-84
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:11828375-Age Factors,
pubmed-meshheading:11828375-Allergens,
pubmed-meshheading:11828375-Animals,
pubmed-meshheading:11828375-Child,
pubmed-meshheading:11828375-Child, Preschool,
pubmed-meshheading:11828375-Female,
pubmed-meshheading:11828375-Humans,
pubmed-meshheading:11828375-Hypersensitivity, Immediate,
pubmed-meshheading:11828375-Immunoglobulin Class Switching,
pubmed-meshheading:11828375-Immunoglobulin E,
pubmed-meshheading:11828375-Immunoglobulin G,
pubmed-meshheading:11828375-Immunoglobulin M,
pubmed-meshheading:11828375-Infant,
pubmed-meshheading:11828375-Male,
pubmed-meshheading:11828375-Models, Immunological,
pubmed-meshheading:11828375-Pollen,
pubmed-meshheading:11828375-Rhinitis, Allergic, Seasonal
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pubmed:year |
2002
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pubmed:articleTitle |
Evolution of IgM, IgE and IgG(1-4 )antibody responses in early childhood monitored with recombinant allergen components: implications for class switch mechanisms.
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pubmed:affiliation |
Department of Otorhinolaryngology, Vienna General Hospital, University of Vienna, Waeringer Guertel 18-20, A-1090 Vienna, Austria.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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