Linked Life Data

3372999

Source:http://linkedlifedata.com/resource/pubmed/id/3372999

Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
12
pubmed:dateCreated
1988-7-12
pubmed:abstractText
The relative binding site location and species specificity of 19 mouse hybridoma antibodies, produced in four laboratories, to Dermatophagoides pteronyssinus major fecal allergen, Der p I, was studied by using immobilized mAb and inhibitions of radiolabeled Ag binding. Four mAb groups were defined, within which 4, 6, 8, and 5 mAb, respectively, cross-inhibited each other. Five mAb were members of both group 2 and 3, demonstrating a considerable overlap of epitopes between the corresponding antibody-binding regions. The degree of mAb species specificity, as assessed by inhibition with cold Der p I and Ag Der m I and Der f I from the related species, Dermatophagoides microceras and Dermatophagoides farinae, was highly variable even for mAb binding to the same region on the Ag. Five cases of cross-reactivity between Der p I and Der m I and one case of cross-reactivity between Der p I and Der f I were found. The N-terminal 30 amino acids of the three species showed 7 substitutions between Der p I and Der m I/Der f I and 2 between Der f I and Der p I/Der m I. Single mAb inhibited up to 65% of labeled Der p I binding to immobilized human IgE from allergic patients' sera and up to 24% of labeled Der p I binding to immobilized rabbit antibodies. The spectrum of species specificities in human IgE sera, as assessed by inhibitions with cold Ag, was similar to that of the mAb. No evidence for the presence of strictly sequential epitopes, reactive with either mAb or human IgE was found, as judged from the weak inhibitory activity of acid-denatured Der p I.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
AIM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jun
pubmed:issn
0022-1767
pubmed:author
pubmed:issnType
Print
pubmed:day
15
pubmed:volume
140
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
4256-62
pubmed:dateRevised
2011-11-17
pubmed:meshHeading
pubmed-meshheading:3372999-Adult, pubmed-meshheading:3372999-Allergens, pubmed-meshheading:3372999-Amino Acid Sequence, pubmed-meshheading:3372999-Animals, pubmed-meshheading:3372999-Antibodies, Monoclonal, pubmed-meshheading:3372999-Antigens, Dermatophagoides, pubmed-meshheading:3372999-Binding, Competitive, pubmed-meshheading:3372999-Binding Sites, Antibody, pubmed-meshheading:3372999-Dose-Response Relationship, Immunologic, pubmed-meshheading:3372999-Humans, pubmed-meshheading:3372999-Immunoglobulin E, pubmed-meshheading:3372999-Immunosuppressive Agents, pubmed-meshheading:3372999-Mice, pubmed-meshheading:3372999-Mice, Inbred BALB C, pubmed-meshheading:3372999-Mites, pubmed-meshheading:3372999-Molecular Sequence Data, pubmed-meshheading:3372999-Protein Denaturation, pubmed-meshheading:3372999-Rabbits, pubmed-meshheading:3372999-Species Specificity
pubmed:year
1988
pubmed:articleTitle
The binding of mouse hybridoma and human IgE antibodies to the major fecal allergen, Der p I, of Dermatophagoides pteronyssinus. Relative binding site location and species specificity studied by solid-phase inhibition assays with radiolabeled antigen.
pubmed:affiliation
ALK Research Group, University of Copenhagen, Denmark.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't