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Ara h 1 CD4+ T cell epitope-based peptides: candidates for a peanut allergy therapeutic.

Identifieur interne : 001C90 ( PubMed/Curation ); précédent : 001C89; suivant : 001C91

Ara h 1 CD4+ T cell epitope-based peptides: candidates for a peanut allergy therapeutic.

Auteurs : S R Prickett [Australie] ; A L Voskamp ; T. Phan ; A. Dacumos-Hill ; S I Mannering ; J M Rolland ; R E O'Hehir

Source :

Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology [ 1365-2222 ] ; 2013.

RBID : pubmed:23711131

Descripteurs français

English descriptors

KwdEn :
- Amino Acid Sequence, Antigens, Plant (immunology), Basophils (immunology), CD4-Positive T-Lymphocytes (immunology), Epitope Mapping, Epitopes, T-Lymphocyte (chemistry), Epitopes, T-Lymphocyte (immunology), Glycoproteins (immunology), Histocompatibility Antigens Class II (immunology), Humans, Immunoglobulin E (blood), Immunoglobulin E (immunology), Lymphocyte Activation (immunology), Membrane Proteins, Molecular Sequence Data, Peanut Hypersensitivity (immunology), Peptides (chemistry), Peptides (immunology), Plant Proteins (immunology).
MESH :
- chemical , blood : Immunoglobulin E.
- chemical , chemistry : Epitopes, T-Lymphocyte, Peptides.
- chemical , immunology : Antigens, Plant, Epitopes, T-Lymphocyte, Glycoproteins, Histocompatibility Antigens Class II, Immunoglobulin E, Peptides, Plant Proteins.
- immunology : Basophils, CD4-Positive T-Lymphocytes, Lymphocyte Activation, Peanut Hypersensitivity.
- Amino Acid Sequence, Epitope Mapping, Humans, Membrane Proteins, Molecular Sequence Data.

Abstract

Peanut allergy is a life-threatening condition; there is currently no cure. While whole allergen extracts are used for specific immunotherapy for many allergies, they can cause severe reactions and even fatalities in peanut allergy.

DOI: 10.1111/cea.12113
PubMed: 23711131

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pubmed:23711131

Le document en format XML

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<term>CD4-Positive T-Lymphocytes (immunology)</term>
<term>Epitope Mapping</term>
<term>Epitopes, T-Lymphocyte (chemistry)</term>
<term>Epitopes, T-Lymphocyte (immunology)</term>
<term>Glycoproteins (immunology)</term>
<term>Histocompatibility Antigens Class II (immunology)</term>
<term>Humans</term>
<term>Immunoglobulin E (blood)</term>
<term>Immunoglobulin E (immunology)</term>
<term>Lymphocyte Activation (immunology)</term>
<term>Membrane Proteins</term>
<term>Molecular Sequence Data</term>
<term>Peanut Hypersensitivity (immunology)</term>
<term>Peptides (chemistry)</term>
<term>Peptides (immunology)</term>
<term>Plant Proteins (immunology)</term>
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<keywords scheme="KwdFr" xml:lang="fr"><term>Activation des lymphocytes (immunologie)</term>
<term>Antigènes d'histocompatibilité de classe II (immunologie)</term>
<term>Antigènes végétaux (immunologie)</term>
<term>Cartographie épitopique</term>
<term>Données de séquences moléculaires</term>
<term>Déterminants antigéniques des lymphocytes T ()</term>
<term>Déterminants antigéniques des lymphocytes T (immunologie)</term>
<term>Glycoprotéines (immunologie)</term>
<term>Granulocytes basophiles (immunologie)</term>
<term>Humains</term>
<term>Hypersensibilité à l'arachide (immunologie)</term>
<term>Immunoglobuline E (immunologie)</term>
<term>Immunoglobuline E (sang)</term>
<term>Lymphocytes T CD4+ (immunologie)</term>
<term>Peptides ()</term>
<term>Peptides (immunologie)</term>
<term>Protéines membranaires</term>
<term>Protéines végétales (immunologie)</term>
<term>Séquence d'acides aminés</term>
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<term>Histocompatibility Antigens Class II</term>
<term>Immunoglobulin E</term>
<term>Peptides</term>
<term>Plant Proteins</term>
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<keywords scheme="MESH" qualifier="immunologie" xml:lang="fr"><term>Activation des lymphocytes</term>
<term>Antigènes d'histocompatibilité de classe II</term>
<term>Antigènes végétaux</term>
<term>Déterminants antigéniques des lymphocytes T</term>
<term>Glycoprotéines</term>
<term>Granulocytes basophiles</term>
<term>Hypersensibilité à l'arachide</term>
<term>Immunoglobuline E</term>
<term>Lymphocytes T CD4+</term>
<term>Peptides</term>
<term>Protéines végétales</term>
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<keywords scheme="MESH" qualifier="immunology" xml:lang="en"><term>Basophils</term>
<term>CD4-Positive T-Lymphocytes</term>
<term>Lymphocyte Activation</term>
<term>Peanut Hypersensitivity</term>
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<keywords scheme="MESH" qualifier="sang" xml:lang="fr"><term>Immunoglobuline E</term>
</keywords>
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<term>Epitope Mapping</term>
<term>Humans</term>
<term>Membrane Proteins</term>
<term>Molecular Sequence Data</term>
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<keywords scheme="MESH" xml:lang="fr"><term>Cartographie épitopique</term>
<term>Données de séquences moléculaires</term>
<term>Déterminants antigéniques des lymphocytes T</term>
<term>Humains</term>
<term>Peptides</term>
<term>Protéines membranaires</term>
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<front><div type="abstract" xml:lang="en">Peanut allergy is a life-threatening condition; there is currently no cure. While whole allergen extracts are used for specific immunotherapy for many allergies, they can cause severe reactions and even fatalities in peanut allergy.</div>
</front>
</TEI>
<pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">23711131</PMID>
<DateCompleted><Year>2014</Year>
<Month>01</Month>
<Day>10</Day>
</DateCompleted>
<DateRevised><Year>2019</Year>
<Month>12</Month>
<Day>10</Day>
</DateRevised>
<Article PubModel="Print"><Journal><ISSN IssnType="Electronic">1365-2222</ISSN>
<JournalIssue CitedMedium="Internet"><Volume>43</Volume>
<Issue>6</Issue>
<PubDate><Year>2013</Year>
<Month>Jun</Month>
</PubDate>
</JournalIssue>
<Title>Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology</Title>
<ISOAbbreviation>Clin. Exp. Allergy</ISOAbbreviation>
</Journal>
<ArticleTitle>Ara h 1 CD4+ T cell epitope-based peptides: candidates for a peanut allergy therapeutic.</ArticleTitle>
<Pagination><MedlinePgn>684-97</MedlinePgn>
</Pagination>
<ELocationID EIdType="doi" ValidYN="Y">10.1111/cea.12113</ELocationID>
<Abstract><AbstractText Label="BACKGROUND" NlmCategory="BACKGROUND">Peanut allergy is a life-threatening condition; there is currently no cure. While whole allergen extracts are used for specific immunotherapy for many allergies, they can cause severe reactions and even fatalities in peanut allergy.</AbstractText>
<AbstractText Label="OBJECTIVE" NlmCategory="OBJECTIVE">To identify short, HLA-degenerate CD4(+) T cell epitope-based peptides of the major peanut allergen Ara h 1 that target allergen-specific T cells without causing IgE-mediated inflammatory cell activation, as candidates for safe peanut-specific immunotherapy.</AbstractText>
<AbstractText Label="METHODS" NlmCategory="METHODS">Ara h 1-specific CD4(+) T cell lines (TCL) were generated from peripheral blood mononuclear cells (PBMC) of peanut-allergic subjects using CFSE-based methodology. T cell epitopes were identified using CFSE and thymidine-based proliferation assays. Epitope HLA-restriction was investigated using blocking antibodies, HLA-genotyping and epitope prediction algorithms. Functional peanut-specific IgE reactivity to peptides was assessed by basophil activation assay.</AbstractText>
<AbstractText Label="RESULTS" NlmCategory="RESULTS">A total of 145 Ara h 1-specific TCL were generated from 18 HLA-diverse peanut-allergic subjects. The TCL recognized 20-mer peptides throughout Ara h 1. Nine 20-mers containing the most frequently recognized epitopes were selected and their recognition confirmed in 18 additional peanut-allergic subjects. Ten core epitopes were mapped within these 20-mers. These were HLA-DQ and/or HLA-DR restricted, with each presented on at least two different HLA-molecules. Seven short (≤ 20 aa) non-basophil-reactive peptides encompassing all core epitopes were designed and validated in peanut-allergic donor PBMC T cell assays.</AbstractText>
<AbstractText Label="CONCLUSIONS AND CLINICAL RELEVANCE" NlmCategory="CONCLUSIONS">Short CD4(+) T cell epitope-based Ara h 1 peptides were identified as novel candidates for a safe, T cell targeted peanut-specific immunotherapy for HLA-diverse populations.</AbstractText>
<CopyrightInformation>© 2013 John Wiley & Sons Ltd.</CopyrightInformation>
</Abstract>
<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Prickett</LastName>
<ForeName>S R</ForeName>
<Initials>SR</Initials>
<AffiliationInfo><Affiliation>Department of Immunology, Monash University, Melbourne, Vic., Australia.</Affiliation>
</AffiliationInfo>
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<Author ValidYN="Y"><LastName>Voskamp</LastName>
<ForeName>A L</ForeName>
<Initials>AL</Initials>
</Author>
<Author ValidYN="Y"><LastName>Phan</LastName>
<ForeName>T</ForeName>
<Initials>T</Initials>
</Author>
<Author ValidYN="Y"><LastName>Dacumos-Hill</LastName>
<ForeName>A</ForeName>
<Initials>A</Initials>
</Author>
<Author ValidYN="Y"><LastName>Mannering</LastName>
<ForeName>S I</ForeName>
<Initials>SI</Initials>
</Author>
<Author ValidYN="Y"><LastName>Rolland</LastName>
<ForeName>J M</ForeName>
<Initials>JM</Initials>
</Author>
<Author ValidYN="Y"><LastName>O'Hehir</LastName>
<ForeName>R E</ForeName>
<Initials>RE</Initials>
</Author>
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<Language>eng</Language>
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<PublicationType UI="D013485">Research Support, Non-U.S. Gov't</PublicationType>
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<MedlineTA>Clin Exp Allergy</MedlineTA>
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<Chemical><RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="C500889">Ara h 1 protein, Arachis hypogaea</NameOfSubstance>
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<MeshHeadingList><MeshHeading><DescriptorName UI="D000595" MajorTopicYN="N">Amino Acid Sequence</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D052179" MajorTopicYN="N">Antigens, Plant</DescriptorName>
<QualifierName UI="Q000276" MajorTopicYN="Y">immunology</QualifierName>
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<MeshHeading><DescriptorName UI="D007073" MajorTopicYN="N">Immunoglobulin E</DescriptorName>
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<MeshHeading><DescriptorName UI="D008213" MajorTopicYN="N">Lymphocyte Activation</DescriptorName>
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<MeshHeading><DescriptorName UI="D008565" MajorTopicYN="N">Membrane Proteins</DescriptorName>
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<MeshHeading><DescriptorName UI="D008969" MajorTopicYN="N">Molecular Sequence Data</DescriptorName>
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<MeshHeading><DescriptorName UI="D010455" MajorTopicYN="N">Peptides</DescriptorName>
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</MeshHeading>
<MeshHeading><DescriptorName UI="D010940" MajorTopicYN="N">Plant Proteins</DescriptorName>
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Ara h 1 CD4+ T cell epitope-based peptides: candidates for a peanut allergy therapeutic.

Ara h 1 CD4+ T cell epitope-based peptides: candidates for a peanut allergy therapeutic.

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