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Oxidation-Specific Epitopes (OSEs) Dominate the B Cell Response in Murine Polymicrobial Sepsis

In murine abdominal sepsis by colon ascendens stent peritonitis (CASP), a strong increase in serum IgM and IgG antibodies was observed, which reached maximum values 14 days following sepsis induction. The specificity of this antibody response was studied in serum and at the single cell level using a...

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Autores principales: Nicolai, Oliver, Pötschke, Christian, Raafat, Dina, van der Linde, Julia, Quosdorf, Sandra, Laqua, Anna, Heidecke, Claus-Dieter, Berek, Claudia, Darisipudi, Murthy N., Binder, Christoph J., Bröker, Barbara M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7412885/
https://www.ncbi.nlm.nih.gov/pubmed/32849533
http://dx.doi.org/10.3389/fimmu.2020.01570
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author Nicolai, Oliver
Pötschke, Christian
Raafat, Dina
van der Linde, Julia
Quosdorf, Sandra
Laqua, Anna
Heidecke, Claus-Dieter
Berek, Claudia
Darisipudi, Murthy N.
Binder, Christoph J.
Bröker, Barbara M.
author_facet Nicolai, Oliver
Pötschke, Christian
Raafat, Dina
van der Linde, Julia
Quosdorf, Sandra
Laqua, Anna
Heidecke, Claus-Dieter
Berek, Claudia
Darisipudi, Murthy N.
Binder, Christoph J.
Bröker, Barbara M.
author_sort Nicolai, Oliver
collection PubMed
description In murine abdominal sepsis by colon ascendens stent peritonitis (CASP), a strong increase in serum IgM and IgG antibodies was observed, which reached maximum values 14 days following sepsis induction. The specificity of this antibody response was studied in serum and at the single cell level using a broad panel of bacterial, sepsis-unrelated as well as self-antigens. Whereas an antibacterial IgM/IgG response was rarely observed, studies at the single-cell level revealed that IgM antibodies, in particular, were largely polyreactive. Interestingly, at least 16% of the IgM mAbs and 20% of the IgG mAbs derived from post-septic mice showed specificity for oxidation-specific epitopes (OSEs), which are known targets of the innate/adaptive immune response. This identifies those self-antigens as the main target of B cell responses in sepsis.
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spelling pubmed-74128852020-08-25 Oxidation-Specific Epitopes (OSEs) Dominate the B Cell Response in Murine Polymicrobial Sepsis Nicolai, Oliver Pötschke, Christian Raafat, Dina van der Linde, Julia Quosdorf, Sandra Laqua, Anna Heidecke, Claus-Dieter Berek, Claudia Darisipudi, Murthy N. Binder, Christoph J. Bröker, Barbara M. Front Immunol Immunology In murine abdominal sepsis by colon ascendens stent peritonitis (CASP), a strong increase in serum IgM and IgG antibodies was observed, which reached maximum values 14 days following sepsis induction. The specificity of this antibody response was studied in serum and at the single cell level using a broad panel of bacterial, sepsis-unrelated as well as self-antigens. Whereas an antibacterial IgM/IgG response was rarely observed, studies at the single-cell level revealed that IgM antibodies, in particular, were largely polyreactive. Interestingly, at least 16% of the IgM mAbs and 20% of the IgG mAbs derived from post-septic mice showed specificity for oxidation-specific epitopes (OSEs), which are known targets of the innate/adaptive immune response. This identifies those self-antigens as the main target of B cell responses in sepsis. Frontiers Media S.A. 2020-07-31 /pmc/articles/PMC7412885/ /pubmed/32849533 http://dx.doi.org/10.3389/fimmu.2020.01570 Text en Copyright © 2020 Nicolai, Pötschke, Raafat, van der Linde, Quosdorf, Laqua, Heidecke, Berek, Darisipudi, Binder and Bröker. 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) and the copyright owner(s) 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
Nicolai, Oliver
Pötschke, Christian
Raafat, Dina
van der Linde, Julia
Quosdorf, Sandra
Laqua, Anna
Heidecke, Claus-Dieter
Berek, Claudia
Darisipudi, Murthy N.
Binder, Christoph J.
Bröker, Barbara M.
Oxidation-Specific Epitopes (OSEs) Dominate the B Cell Response in Murine Polymicrobial Sepsis
title Oxidation-Specific Epitopes (OSEs) Dominate the B Cell Response in Murine Polymicrobial Sepsis
title_full Oxidation-Specific Epitopes (OSEs) Dominate the B Cell Response in Murine Polymicrobial Sepsis
title_fullStr Oxidation-Specific Epitopes (OSEs) Dominate the B Cell Response in Murine Polymicrobial Sepsis
title_full_unstemmed Oxidation-Specific Epitopes (OSEs) Dominate the B Cell Response in Murine Polymicrobial Sepsis
title_short Oxidation-Specific Epitopes (OSEs) Dominate the B Cell Response in Murine Polymicrobial Sepsis
title_sort oxidation-specific epitopes (oses) dominate the b cell response in murine polymicrobial sepsis
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7412885/
https://www.ncbi.nlm.nih.gov/pubmed/32849533
http://dx.doi.org/10.3389/fimmu.2020.01570
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