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IgE and IgG4 epitope mapping by microarray immunoassay reveals the diversity of immune response to the peanut allergen, Ara h 2.

Identifieur interne : 000374 ( Ncbi/Merge ); précédent : 000373; suivant : 000375

IgE and IgG4 epitope mapping by microarray immunoassay reveals the diversity of immune response to the peanut allergen, Ara h 2.

Auteurs : Wayne G. Shreffler [États-Unis] ; Doerthe A. Lencer ; Ludmilla Bardina ; Hugh A. Sampson

Source :

RBID : pubmed:16210066

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English descriptors

Abstract

Detailed assessment of antibody responses to allergens reveals clinically relevant information about both host response and antigen structure. Microarray technology offers advantages of scale and parallel design over previous methods of epitope mapping.

DOI: 10.1016/j.jaci.2005.06.033
PubMed: 16210066

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pubmed:16210066

Le document en format XML

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<term>Allergens (immunology)</term>
<term>Amino Acid Sequence</term>
<term>Antibody Specificity</term>
<term>Antigen-Antibody Reactions</term>
<term>Antigens, Plant</term>
<term>Arachis (genetics)</term>
<term>Arachis (immunology)</term>
<term>Case-Control Studies</term>
<term>Cluster Analysis</term>
<term>Epitope Mapping (methods)</term>
<term>Epitope Mapping (statistics & numerical data)</term>
<term>Glycoproteins (genetics)</term>
<term>Glycoproteins (immunology)</term>
<term>Humans</term>
<term>Immunoglobulin E (metabolism)</term>
<term>Immunoglobulin G (metabolism)</term>
<term>In Vitro Techniques</term>
<term>Molecular Sequence Data</term>
<term>Peanut Hypersensitivity (genetics)</term>
<term>Peanut Hypersensitivity (immunology)</term>
<term>Plant Proteins (genetics)</term>
<term>Plant Proteins (immunology)</term>
<term>Protein Array Analysis</term>
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<keywords scheme="KwdFr" xml:lang="fr">
<term>Albumines 2S de plante</term>
<term>Allergènes (génétique)</term>
<term>Allergènes (immunologie)</term>
<term>Analyse de regroupements</term>
<term>Analyse par réseau de protéines</term>
<term>Antigènes végétaux</term>
<term>Arachis (génétique)</term>
<term>Arachis (immunologie)</term>
<term>Cartographie épitopique ()</term>
<term>Données de séquences moléculaires</term>
<term>Glycoprotéines (génétique)</term>
<term>Glycoprotéines (immunologie)</term>
<term>Humains</term>
<term>Hypersensibilité à l'arachide (génétique)</term>
<term>Hypersensibilité à l'arachide (immunologie)</term>
<term>Immunoglobuline E (métabolisme)</term>
<term>Immunoglobuline G (métabolisme)</term>
<term>Protéines végétales (génétique)</term>
<term>Protéines végétales (immunologie)</term>
<term>Réaction antigène-anticorps</term>
<term>Spécificité des anticorps</term>
<term>Séquence d'acides aminés</term>
<term>Techniques in vitro</term>
<term>Études cas-témoins</term>
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<keywords scheme="MESH" type="chemical" qualifier="genetics" xml:lang="en">
<term>Allergens</term>
<term>Glycoproteins</term>
<term>Plant Proteins</term>
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<term>Allergens</term>
<term>Glycoproteins</term>
<term>Plant Proteins</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="metabolism" xml:lang="en">
<term>Immunoglobulin E</term>
<term>Immunoglobulin G</term>
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<term>2S Albumins, Plant</term>
<term>Antigens, Plant</term>
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<keywords scheme="MESH" qualifier="genetics" xml:lang="en">
<term>Arachis</term>
<term>Peanut Hypersensitivity</term>
</keywords>
<keywords scheme="MESH" qualifier="génétique" xml:lang="fr">
<term>Allergènes</term>
<term>Arachis</term>
<term>Glycoprotéines</term>
<term>Hypersensibilité à l'arachide</term>
<term>Protéines végétales</term>
</keywords>
<keywords scheme="MESH" qualifier="immunologie" xml:lang="fr">
<term>Allergènes</term>
<term>Arachis</term>
<term>Glycoprotéines</term>
<term>Hypersensibilité à l'arachide</term>
<term>Protéines végétales</term>
</keywords>
<keywords scheme="MESH" qualifier="immunology" xml:lang="en">
<term>Arachis</term>
<term>Peanut Hypersensitivity</term>
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<keywords scheme="MESH" qualifier="methods" xml:lang="en">
<term>Epitope Mapping</term>
</keywords>
<keywords scheme="MESH" qualifier="métabolisme" xml:lang="fr">
<term>Immunoglobuline E</term>
<term>Immunoglobuline G</term>
</keywords>
<keywords scheme="MESH" qualifier="statistics & numerical data" xml:lang="en">
<term>Epitope Mapping</term>
</keywords>
<keywords scheme="MESH" xml:lang="en">
<term>Amino Acid Sequence</term>
<term>Antibody Specificity</term>
<term>Antigen-Antibody Reactions</term>
<term>Case-Control Studies</term>
<term>Cluster Analysis</term>
<term>Humans</term>
<term>In Vitro Techniques</term>
<term>Molecular Sequence Data</term>
<term>Protein Array Analysis</term>
</keywords>
<keywords scheme="MESH" xml:lang="fr">
<term>Albumines 2S de plante</term>
<term>Analyse de regroupements</term>
<term>Analyse par réseau de protéines</term>
<term>Antigènes végétaux</term>
<term>Cartographie épitopique</term>
<term>Données de séquences moléculaires</term>
<term>Humains</term>
<term>Réaction antigène-anticorps</term>
<term>Spécificité des anticorps</term>
<term>Séquence d'acides aminés</term>
<term>Techniques in vitro</term>
<term>Études cas-témoins</term>
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<front>
<div type="abstract" xml:lang="en">Detailed assessment of antibody responses to allergens reveals clinically relevant information about both host response and antigen structure. Microarray technology offers advantages of scale and parallel design over previous methods of epitope mapping.</div>
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<PMID Version="1">16210066</PMID>
<DateCompleted>
<Year>2005</Year>
<Month>11</Month>
<Day>21</Day>
</DateCompleted>
<DateRevised>
<Year>2015</Year>
<Month>11</Month>
<Day>19</Day>
</DateRevised>
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<Journal>
<ISSN IssnType="Print">0091-6749</ISSN>
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<Volume>116</Volume>
<Issue>4</Issue>
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<Year>2005</Year>
<Month>Oct</Month>
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<Title>The Journal of allergy and clinical immunology</Title>
<ISOAbbreviation>J. Allergy Clin. Immunol.</ISOAbbreviation>
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<ArticleTitle>IgE and IgG4 epitope mapping by microarray immunoassay reveals the diversity of immune response to the peanut allergen, Ara h 2.</ArticleTitle>
<Pagination>
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<Abstract>
<AbstractText Label="BACKGROUND" NlmCategory="BACKGROUND">Detailed assessment of antibody responses to allergens reveals clinically relevant information about both host response and antigen structure. Microarray technology offers advantages of scale and parallel design over previous methods of epitope mapping.</AbstractText>
<AbstractText Label="OBJECTIVE" NlmCategory="OBJECTIVE">We designed a redundant peptide microarray for IgE and IgG4 epitope mapping of the previously characterized peanut allergen, Ara h 2.</AbstractText>
<AbstractText Label="METHODS" NlmCategory="METHODS">Six complete sets of overlapping peptides were commercially synthesized and site-specifically bound to epoxy-derivatized glass slides in triplicate. Peptides were 10, 15, or 20 amino acids in length with an offset of either 2 or 3 amino acids. A total of 10 control and 45 peanut-allergic sera were assayed. Specific IgE and IgG4 were detected by using fluorochrome-labeled monoclonal secondary antibodies.</AbstractText>
<AbstractText Label="RESULTS" NlmCategory="RESULTS">By using 15-mer and 20-mer peptides, we could define 11 antigenic regions, whereas only 5 were identifiable using 10-mers. Controls and patients produced IgG4 recognizing a comparable number of Ara h 2 peptides, although the dominant epitopes were distinct. As expected, patient IgE bound a larger number of Ara h 2 peptides (9.4% vs 0.9%). IgE and IgG4 epitopes recognized by patients were largely the same, and there was a positive association between IgE and IgG(4) signal, suggesting coordinate regulation. Cluster analysis of peptide binding patterns confirmed the specificity of antibody-peptide interactions and was used to define 9 core epitopes ranging from 6 to 16 residues in length-7 of which (78%) agreed with previous mapping.</AbstractText>
<AbstractText Label="CONCLUSION" NlmCategory="CONCLUSIONS">Epitope mapping by microarray peptide immunoassay and cluster analysis reveals interpatient heterogeneity and a more detailed map.</AbstractText>
</Abstract>
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<LastName>Shreffler</LastName>
<ForeName>Wayne G</ForeName>
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<Affiliation>Jaffe Food Allergy Institute, Department of Pediatrics, Division of Allergy and Immunology, Mount Sinai School of Medicine, New York, NY 10029, USA. wayne.shreffler@mssm.edu</Affiliation>
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<ForeName>Ludmilla</ForeName>
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<LastName>Sampson</LastName>
<ForeName>Hugh A</ForeName>
<Initials>HA</Initials>
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<GrantID>M01-RR-00071</GrantID>
<Acronym>RR</Acronym>
<Agency>NCRR NIH HHS</Agency>
<Country>United States</Country>
</Grant>
<Grant>
<GrantID>P01-AI44236-01</GrantID>
<Acronym>AI</Acronym>
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<Country>United States</Country>
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<Chemical>
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<NameOfSubstance UI="C500890">Ara h 2 allergen, Arachis hypogaea</NameOfSubstance>
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<CitationSubset>IM</CitationSubset>
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<DescriptorName UI="D055516" MajorTopicYN="N">2S Albumins, Plant</DescriptorName>
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<DescriptorName UI="D000485" MajorTopicYN="N">Allergens</DescriptorName>
<QualifierName UI="Q000235" MajorTopicYN="Y">genetics</QualifierName>
<QualifierName UI="Q000276" MajorTopicYN="Y">immunology</QualifierName>
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