Cargando…
Anti-amyloidogenic Activity of IgGs Contained in Normal Plasma
INTRODUCTION: We have previously shown that a subpopulation of naturally occurring human IgGs has therapeutic potential for the amyloid-associated disorders. These molecules cross-react with conformational epitopes on amyloidogenic assemblies, including amyloid beta (Aβ) protein fibrils that are a p...
Autores principales: | , , , , , , , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
Springer US
2010
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2883095/ https://www.ncbi.nlm.nih.gov/pubmed/20405179 http://dx.doi.org/10.1007/s10875-010-9413-6 |
_version_ | 1782182233693487104 |
---|---|
author | O’Nuallain, Brian Williams, Angela D. McWilliams-Koeppen, Helen P. Acero, Luis Weber, Alfred Ehrlich, Hartmut Schwarz, Hans P. Solomon, Alan |
author_facet | O’Nuallain, Brian Williams, Angela D. McWilliams-Koeppen, Helen P. Acero, Luis Weber, Alfred Ehrlich, Hartmut Schwarz, Hans P. Solomon, Alan |
author_sort | O’Nuallain, Brian |
collection | PubMed |
description | INTRODUCTION: We have previously shown that a subpopulation of naturally occurring human IgGs has therapeutic potential for the amyloid-associated disorders. These molecules cross-react with conformational epitopes on amyloidogenic assemblies, including amyloid beta (Aβ) protein fibrils that are a pathological hallmark of Alzheimer’s disease. MATERIALS AND METHODS: Using our europium-linked immunosorbant assay, we established that ∼95% of 260 screened donor plasma samples had amyloid fibril-reactive IgGs and Aβ conformer-reactive IgGs with minimal binding to Aβ monomers. Anti-amyloidogenic reactivity was diverse and attributed to Aβ targeting multiple fibril-related binding sites and/or variations in multidentate binding. RESULTS AND DISCUSSION: There was no correlation between anti-fibril and anti-oligomer reactivity and donor age (19 to 60 years old) or gender. These findings demonstrate the inherent but diverse anti-amyloidogenic activity of natural IgGs contained in normal plasma. CONCLUSION: Our studies provide support for investigating the clinical significance and physiological function of this novel class of antibodies. |
format | Text |
id | pubmed-2883095 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-28830952010-06-21 Anti-amyloidogenic Activity of IgGs Contained in Normal Plasma O’Nuallain, Brian Williams, Angela D. McWilliams-Koeppen, Helen P. Acero, Luis Weber, Alfred Ehrlich, Hartmut Schwarz, Hans P. Solomon, Alan J Clin Immunol Article INTRODUCTION: We have previously shown that a subpopulation of naturally occurring human IgGs has therapeutic potential for the amyloid-associated disorders. These molecules cross-react with conformational epitopes on amyloidogenic assemblies, including amyloid beta (Aβ) protein fibrils that are a pathological hallmark of Alzheimer’s disease. MATERIALS AND METHODS: Using our europium-linked immunosorbant assay, we established that ∼95% of 260 screened donor plasma samples had amyloid fibril-reactive IgGs and Aβ conformer-reactive IgGs with minimal binding to Aβ monomers. Anti-amyloidogenic reactivity was diverse and attributed to Aβ targeting multiple fibril-related binding sites and/or variations in multidentate binding. RESULTS AND DISCUSSION: There was no correlation between anti-fibril and anti-oligomer reactivity and donor age (19 to 60 years old) or gender. These findings demonstrate the inherent but diverse anti-amyloidogenic activity of natural IgGs contained in normal plasma. CONCLUSION: Our studies provide support for investigating the clinical significance and physiological function of this novel class of antibodies. Springer US 2010-04-20 2010-05 /pmc/articles/PMC2883095/ /pubmed/20405179 http://dx.doi.org/10.1007/s10875-010-9413-6 Text en © Springer Science+Business Media, LLC 2010 |
spellingShingle | Article O’Nuallain, Brian Williams, Angela D. McWilliams-Koeppen, Helen P. Acero, Luis Weber, Alfred Ehrlich, Hartmut Schwarz, Hans P. Solomon, Alan Anti-amyloidogenic Activity of IgGs Contained in Normal Plasma |
title | Anti-amyloidogenic Activity of IgGs Contained in Normal Plasma |
title_full | Anti-amyloidogenic Activity of IgGs Contained in Normal Plasma |
title_fullStr | Anti-amyloidogenic Activity of IgGs Contained in Normal Plasma |
title_full_unstemmed | Anti-amyloidogenic Activity of IgGs Contained in Normal Plasma |
title_short | Anti-amyloidogenic Activity of IgGs Contained in Normal Plasma |
title_sort | anti-amyloidogenic activity of iggs contained in normal plasma |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2883095/ https://www.ncbi.nlm.nih.gov/pubmed/20405179 http://dx.doi.org/10.1007/s10875-010-9413-6 |
work_keys_str_mv | AT onuallainbrian antiamyloidogenicactivityofiggscontainedinnormalplasma AT williamsangelad antiamyloidogenicactivityofiggscontainedinnormalplasma AT mcwilliamskoeppenhelenp antiamyloidogenicactivityofiggscontainedinnormalplasma AT aceroluis antiamyloidogenicactivityofiggscontainedinnormalplasma AT weberalfred antiamyloidogenicactivityofiggscontainedinnormalplasma AT ehrlichhartmut antiamyloidogenicactivityofiggscontainedinnormalplasma AT schwarzhansp antiamyloidogenicactivityofiggscontainedinnormalplasma AT solomonalan antiamyloidogenicactivityofiggscontainedinnormalplasma |