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Usefulness of the Nonself-Self Algorithm of HLA Epitope Immunogenicity in the Specificity Analysis of Monospecific Antibodies Induced during Pregnancy

BACKGROUND: HLAMatchmaker is a program to analyze the epitope specificities of HLA antibodies. It considers each HLA allele as a string of eplets. Intralocus and interlocus comparisons between donor and recipient alleles offer a structural assessment of compatibility and an analysis of allele panel...

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Autores principales: Duquesnoy, Rene J., Marrari, Marilyn, Mulder, Arend
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4443772/
https://www.ncbi.nlm.nih.gov/pubmed/26074914
http://dx.doi.org/10.3389/fimmu.2015.00180
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author Duquesnoy, Rene J.
Marrari, Marilyn
Mulder, Arend
author_facet Duquesnoy, Rene J.
Marrari, Marilyn
Mulder, Arend
author_sort Duquesnoy, Rene J.
collection PubMed
description BACKGROUND: HLAMatchmaker is a program to analyze the epitope specificities of HLA antibodies. It considers each HLA allele as a string of eplets. Intralocus and interlocus comparisons between donor and recipient alleles offer a structural assessment of compatibility and an analysis of allele panel reactivity patterns can generate information about epitope specificities of HLA antibodies. However, HLAMatchmaker cannot always generate conclusive interpretations of reactivity patterns of all monospecific antibodies, which by definition recognize single epitopes. HYPOTHESIS: We have therefore developed a new antibody analysis approach that utilizes the nonself–self algorithm of HLA epitope immunogenicity. It is based on the concept that HLA antibodies originate from B-cells with immunoglobulin receptors to self-HLA epitopes on one given allele and which can be activated by epitopes defined by a few nonself residue differences whereas the remainder of the structural epitope of the immunizing allele consists of self residues. METHODS: Three human monoclonal class I antibodies from HLA typed women sensitized during pregnancy were tested in Ig-binding assays with single alleles on a Luminex platform. FINDINGS: Three new HLA epitopes were identified; they are defined by combinations of nonself- and self-residues for one allele of the antibody producer. CONCLUSION: The nonself–self paradigm of HLA epitope immunogenicity offers a second approach to analyze HLA antibody specificities.
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spelling pubmed-44437722015-06-12 Usefulness of the Nonself-Self Algorithm of HLA Epitope Immunogenicity in the Specificity Analysis of Monospecific Antibodies Induced during Pregnancy Duquesnoy, Rene J. Marrari, Marilyn Mulder, Arend Front Immunol Immunology BACKGROUND: HLAMatchmaker is a program to analyze the epitope specificities of HLA antibodies. It considers each HLA allele as a string of eplets. Intralocus and interlocus comparisons between donor and recipient alleles offer a structural assessment of compatibility and an analysis of allele panel reactivity patterns can generate information about epitope specificities of HLA antibodies. However, HLAMatchmaker cannot always generate conclusive interpretations of reactivity patterns of all monospecific antibodies, which by definition recognize single epitopes. HYPOTHESIS: We have therefore developed a new antibody analysis approach that utilizes the nonself–self algorithm of HLA epitope immunogenicity. It is based on the concept that HLA antibodies originate from B-cells with immunoglobulin receptors to self-HLA epitopes on one given allele and which can be activated by epitopes defined by a few nonself residue differences whereas the remainder of the structural epitope of the immunizing allele consists of self residues. METHODS: Three human monoclonal class I antibodies from HLA typed women sensitized during pregnancy were tested in Ig-binding assays with single alleles on a Luminex platform. FINDINGS: Three new HLA epitopes were identified; they are defined by combinations of nonself- and self-residues for one allele of the antibody producer. CONCLUSION: The nonself–self paradigm of HLA epitope immunogenicity offers a second approach to analyze HLA antibody specificities. Frontiers Media S.A. 2015-05-26 /pmc/articles/PMC4443772/ /pubmed/26074914 http://dx.doi.org/10.3389/fimmu.2015.00180 Text en Copyright © 2015 Duquesnoy, Marrari and Mulder. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Duquesnoy, Rene J.
Marrari, Marilyn
Mulder, Arend
Usefulness of the Nonself-Self Algorithm of HLA Epitope Immunogenicity in the Specificity Analysis of Monospecific Antibodies Induced during Pregnancy
title Usefulness of the Nonself-Self Algorithm of HLA Epitope Immunogenicity in the Specificity Analysis of Monospecific Antibodies Induced during Pregnancy
title_full Usefulness of the Nonself-Self Algorithm of HLA Epitope Immunogenicity in the Specificity Analysis of Monospecific Antibodies Induced during Pregnancy
title_fullStr Usefulness of the Nonself-Self Algorithm of HLA Epitope Immunogenicity in the Specificity Analysis of Monospecific Antibodies Induced during Pregnancy
title_full_unstemmed Usefulness of the Nonself-Self Algorithm of HLA Epitope Immunogenicity in the Specificity Analysis of Monospecific Antibodies Induced during Pregnancy
title_short Usefulness of the Nonself-Self Algorithm of HLA Epitope Immunogenicity in the Specificity Analysis of Monospecific Antibodies Induced during Pregnancy
title_sort usefulness of the nonself-self algorithm of hla epitope immunogenicity in the specificity analysis of monospecific antibodies induced during pregnancy
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4443772/
https://www.ncbi.nlm.nih.gov/pubmed/26074914
http://dx.doi.org/10.3389/fimmu.2015.00180
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