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Mimicry of human IgE epitopes by anti-idiotypic antibodies

According to Jerne’s network hypothesis, the binding site of an anti-idiotypic antibody also represents the internal image of an epitope present on a foreign, or even a self antigen. In recent years, antigen mimicry has been defined at the molecular level for some xeno-antigens. However, until now t...

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Autores principales: Vogel, Monique, Miescher, Sylvia, Kuhn, Sonja, Zürcher, Adrian W., Stadler, Michael B., Ruf, Christine, Effenberger, Friedrich, Kricek, Franz, Stadler, Beda M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Academic Press. 2000
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7125776/
https://www.ncbi.nlm.nih.gov/pubmed/10801344
http://dx.doi.org/10.1006/jmbi.2000.3713
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author Vogel, Monique
Miescher, Sylvia
Kuhn, Sonja
Zürcher, Adrian W.
Stadler, Michael B.
Ruf, Christine
Effenberger, Friedrich
Kricek, Franz
Stadler, Beda M.
author_facet Vogel, Monique
Miescher, Sylvia
Kuhn, Sonja
Zürcher, Adrian W.
Stadler, Michael B.
Ruf, Christine
Effenberger, Friedrich
Kricek, Franz
Stadler, Beda M.
author_sort Vogel, Monique
collection PubMed
description According to Jerne’s network hypothesis, the binding site of an anti-idiotypic antibody also represents the internal image of an epitope present on a foreign, or even a self antigen. In recent years, antigen mimicry has been defined at the molecular level for some xeno-antigens. However, until now there has been no demonstration of structural mimicry between a human anti-idiotypic antibody and a self structure. To address this question, we used human IgE as the self structure and a well-defined anti-human IgE mAb (BSW17). We describe the isolation of two anti- idiotypic antibodies specific for the anti-IgE antibody BSW17 from a non-immune human Fab phage display library. Interestingly, these two anti-idiotypic antibodies mimic the same molecular surface region as a previously described IgE peptide mimotope isolated by panning on BSW17, but they cover a much larger epitope on the IgE molecule. Accordingly, immunisation of rabbits with the two anti-idiotypic antibodies induced high-affinity antibodies with the same characteristics as BSW17. Thus, our data demonstrate that it is possible to isolate anti-idiotypic antibodies derived from the human genome without the need for hyperimmunisation, and confirm Jerne’s hypothesis that both foreign antigens and self structures can be mimicked by our own immunoglobulins.
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spelling pubmed-71257762020-04-08 Mimicry of human IgE epitopes by anti-idiotypic antibodies Vogel, Monique Miescher, Sylvia Kuhn, Sonja Zürcher, Adrian W. Stadler, Michael B. Ruf, Christine Effenberger, Friedrich Kricek, Franz Stadler, Beda M. J Mol Biol Communication According to Jerne’s network hypothesis, the binding site of an anti-idiotypic antibody also represents the internal image of an epitope present on a foreign, or even a self antigen. In recent years, antigen mimicry has been defined at the molecular level for some xeno-antigens. However, until now there has been no demonstration of structural mimicry between a human anti-idiotypic antibody and a self structure. To address this question, we used human IgE as the self structure and a well-defined anti-human IgE mAb (BSW17). We describe the isolation of two anti- idiotypic antibodies specific for the anti-IgE antibody BSW17 from a non-immune human Fab phage display library. Interestingly, these two anti-idiotypic antibodies mimic the same molecular surface region as a previously described IgE peptide mimotope isolated by panning on BSW17, but they cover a much larger epitope on the IgE molecule. Accordingly, immunisation of rabbits with the two anti-idiotypic antibodies induced high-affinity antibodies with the same characteristics as BSW17. Thus, our data demonstrate that it is possible to isolate anti-idiotypic antibodies derived from the human genome without the need for hyperimmunisation, and confirm Jerne’s hypothesis that both foreign antigens and self structures can be mimicked by our own immunoglobulins. Academic Press. 2000-05-19 2002-05-25 /pmc/articles/PMC7125776/ /pubmed/10801344 http://dx.doi.org/10.1006/jmbi.2000.3713 Text en Copyright © 2000 Academic Press. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Communication
Vogel, Monique
Miescher, Sylvia
Kuhn, Sonja
Zürcher, Adrian W.
Stadler, Michael B.
Ruf, Christine
Effenberger, Friedrich
Kricek, Franz
Stadler, Beda M.
Mimicry of human IgE epitopes by anti-idiotypic antibodies
title Mimicry of human IgE epitopes by anti-idiotypic antibodies
title_full Mimicry of human IgE epitopes by anti-idiotypic antibodies
title_fullStr Mimicry of human IgE epitopes by anti-idiotypic antibodies
title_full_unstemmed Mimicry of human IgE epitopes by anti-idiotypic antibodies
title_short Mimicry of human IgE epitopes by anti-idiotypic antibodies
title_sort mimicry of human ige epitopes by anti-idiotypic antibodies
topic Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7125776/
https://www.ncbi.nlm.nih.gov/pubmed/10801344
http://dx.doi.org/10.1006/jmbi.2000.3713
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