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Abundant human anti-Galα3Gal antibodies display broad pathogen reactivity
Antibodies of the IgG class to terminal Galα3Gal (IgG anti-αGal) is abundant in human plasma and are reported to bind most sepsis-causing Gram-negative bacteria. However, these seminal findings, made more than two decades ago, have not been reexamined. Our aim was to assess IgG anti-αGal´s pathogen...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7067764/ https://www.ncbi.nlm.nih.gov/pubmed/32165720 http://dx.doi.org/10.1038/s41598-020-61632-9 |
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author | Bernth Jensen, Jens Magnus Petersen, Mikkel Steen Ellerman-Eriksen, Svend Møller, Bjarne Kuno Jensenius, Jens Christian Sørensen, Uffe B. Skov Thiel, Steffen |
author_facet | Bernth Jensen, Jens Magnus Petersen, Mikkel Steen Ellerman-Eriksen, Svend Møller, Bjarne Kuno Jensenius, Jens Christian Sørensen, Uffe B. Skov Thiel, Steffen |
author_sort | Bernth Jensen, Jens Magnus |
collection | PubMed |
description | Antibodies of the IgG class to terminal Galα3Gal (IgG anti-αGal) is abundant in human plasma and are reported to bind most sepsis-causing Gram-negative bacteria. However, these seminal findings, made more than two decades ago, have not been reexamined. Our aim was to assess IgG anti-αGal´s pathogen reactivity. We affinity purified IgG anti-αGal from a therapeutic grade normal human IgG pool applying two rounds of positive selection with Galα3Gal-coupled beads and included removal of column matrix reactive antibodies. The purified antibodies were rigorously characterized in terms of specificity and purity in various solid-phase immunoassays. We used flow cytometry to study reactivity against 100 consecutive clinical isolates diagnosed as cause of sepsis in humans. We found that the purified IgG anti-αGal displays high specificity for Galα3Gal. Also, IgG anti-αGal at 5 mg/L bound 56 out of 100 pathogens with predilection for Gram-positive bacteria binding 39 out of 52 strains. We confirm that although IgG anti-αGal comprise a small fraction of the human antibody pool (~0.1%), these antibodies targets an impressively large part of pathogens causing invasive disease. |
format | Online Article Text |
id | pubmed-7067764 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-70677642020-03-19 Abundant human anti-Galα3Gal antibodies display broad pathogen reactivity Bernth Jensen, Jens Magnus Petersen, Mikkel Steen Ellerman-Eriksen, Svend Møller, Bjarne Kuno Jensenius, Jens Christian Sørensen, Uffe B. Skov Thiel, Steffen Sci Rep Article Antibodies of the IgG class to terminal Galα3Gal (IgG anti-αGal) is abundant in human plasma and are reported to bind most sepsis-causing Gram-negative bacteria. However, these seminal findings, made more than two decades ago, have not been reexamined. Our aim was to assess IgG anti-αGal´s pathogen reactivity. We affinity purified IgG anti-αGal from a therapeutic grade normal human IgG pool applying two rounds of positive selection with Galα3Gal-coupled beads and included removal of column matrix reactive antibodies. The purified antibodies were rigorously characterized in terms of specificity and purity in various solid-phase immunoassays. We used flow cytometry to study reactivity against 100 consecutive clinical isolates diagnosed as cause of sepsis in humans. We found that the purified IgG anti-αGal displays high specificity for Galα3Gal. Also, IgG anti-αGal at 5 mg/L bound 56 out of 100 pathogens with predilection for Gram-positive bacteria binding 39 out of 52 strains. We confirm that although IgG anti-αGal comprise a small fraction of the human antibody pool (~0.1%), these antibodies targets an impressively large part of pathogens causing invasive disease. Nature Publishing Group UK 2020-03-12 /pmc/articles/PMC7067764/ /pubmed/32165720 http://dx.doi.org/10.1038/s41598-020-61632-9 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Bernth Jensen, Jens Magnus Petersen, Mikkel Steen Ellerman-Eriksen, Svend Møller, Bjarne Kuno Jensenius, Jens Christian Sørensen, Uffe B. Skov Thiel, Steffen Abundant human anti-Galα3Gal antibodies display broad pathogen reactivity |
title | Abundant human anti-Galα3Gal antibodies display broad pathogen reactivity |
title_full | Abundant human anti-Galα3Gal antibodies display broad pathogen reactivity |
title_fullStr | Abundant human anti-Galα3Gal antibodies display broad pathogen reactivity |
title_full_unstemmed | Abundant human anti-Galα3Gal antibodies display broad pathogen reactivity |
title_short | Abundant human anti-Galα3Gal antibodies display broad pathogen reactivity |
title_sort | abundant human anti-galα3gal antibodies display broad pathogen reactivity |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7067764/ https://www.ncbi.nlm.nih.gov/pubmed/32165720 http://dx.doi.org/10.1038/s41598-020-61632-9 |
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