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High-resolution physicochemical characterization of different intravenous immunoglobulin products

Intravenous immunoglobulin (IVIg) is a complex mixture drug comprising diverse immunoglobulins and non–IgG proteins purified from the plasma of thousands of healthy donors. Approved IVIg products on the market differ regarding source of plasma, isolation process, and formulation. These products are...

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Autores principales: Washburn, Nathaniel, Meccariello, Robin, Hu, Shaohui, Hains, Maurice, Bhatnagar, Naveen, Sarvaiya, Hetal, Kapoor, Bulbul, Schaeck, John, Pino, Ignacio, Manning, Anthony, Lansing, Jonathan C., Bosques, Carlos J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5536303/
https://www.ncbi.nlm.nih.gov/pubmed/28759653
http://dx.doi.org/10.1371/journal.pone.0181251
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author Washburn, Nathaniel
Meccariello, Robin
Hu, Shaohui
Hains, Maurice
Bhatnagar, Naveen
Sarvaiya, Hetal
Kapoor, Bulbul
Schaeck, John
Pino, Ignacio
Manning, Anthony
Lansing, Jonathan C.
Bosques, Carlos J.
author_facet Washburn, Nathaniel
Meccariello, Robin
Hu, Shaohui
Hains, Maurice
Bhatnagar, Naveen
Sarvaiya, Hetal
Kapoor, Bulbul
Schaeck, John
Pino, Ignacio
Manning, Anthony
Lansing, Jonathan C.
Bosques, Carlos J.
author_sort Washburn, Nathaniel
collection PubMed
description Intravenous immunoglobulin (IVIg) is a complex mixture drug comprising diverse immunoglobulins and non–IgG proteins purified from the plasma of thousands of healthy donors. Approved IVIg products on the market differ regarding source of plasma, isolation process, and formulation. These products are used widely, and often interchangeably, for the treatment of immunodeficiency and autoimmune and inflammatory diseases, but their mechanisms of action in different indications are not well understood. A primary limitation to understanding the therapeutic relevance of specific components within IVIg has been the limited resolution of analytics historically implemented to characterize its complex mixture. In this study, high-resolution analytics were applied to better understand the composition of IVIg and product variations. We characterized three approved IVIg products: Gammagard(®), Privigen(®), and Octagam(®). Differences in the distribution of molecular weight species, IgG sequence variants, isoforms, glycoforms, and the repertoire of previously reported antibody specificities were identified. We also compared the effect of aging on these products to identify changes in size distribution and posttranslational modifications. This type of characterization may provide insights into the specific factors and components of IVIg that may influence its activity and ultimately lead to optimization of IVIg products for use in autoimmune diseases.
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spelling pubmed-55363032017-08-07 High-resolution physicochemical characterization of different intravenous immunoglobulin products Washburn, Nathaniel Meccariello, Robin Hu, Shaohui Hains, Maurice Bhatnagar, Naveen Sarvaiya, Hetal Kapoor, Bulbul Schaeck, John Pino, Ignacio Manning, Anthony Lansing, Jonathan C. Bosques, Carlos J. PLoS One Research Article Intravenous immunoglobulin (IVIg) is a complex mixture drug comprising diverse immunoglobulins and non–IgG proteins purified from the plasma of thousands of healthy donors. Approved IVIg products on the market differ regarding source of plasma, isolation process, and formulation. These products are used widely, and often interchangeably, for the treatment of immunodeficiency and autoimmune and inflammatory diseases, but their mechanisms of action in different indications are not well understood. A primary limitation to understanding the therapeutic relevance of specific components within IVIg has been the limited resolution of analytics historically implemented to characterize its complex mixture. In this study, high-resolution analytics were applied to better understand the composition of IVIg and product variations. We characterized three approved IVIg products: Gammagard(®), Privigen(®), and Octagam(®). Differences in the distribution of molecular weight species, IgG sequence variants, isoforms, glycoforms, and the repertoire of previously reported antibody specificities were identified. We also compared the effect of aging on these products to identify changes in size distribution and posttranslational modifications. This type of characterization may provide insights into the specific factors and components of IVIg that may influence its activity and ultimately lead to optimization of IVIg products for use in autoimmune diseases. Public Library of Science 2017-07-31 /pmc/articles/PMC5536303/ /pubmed/28759653 http://dx.doi.org/10.1371/journal.pone.0181251 Text en © 2017 Washburn et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Washburn, Nathaniel
Meccariello, Robin
Hu, Shaohui
Hains, Maurice
Bhatnagar, Naveen
Sarvaiya, Hetal
Kapoor, Bulbul
Schaeck, John
Pino, Ignacio
Manning, Anthony
Lansing, Jonathan C.
Bosques, Carlos J.
High-resolution physicochemical characterization of different intravenous immunoglobulin products
title High-resolution physicochemical characterization of different intravenous immunoglobulin products
title_full High-resolution physicochemical characterization of different intravenous immunoglobulin products
title_fullStr High-resolution physicochemical characterization of different intravenous immunoglobulin products
title_full_unstemmed High-resolution physicochemical characterization of different intravenous immunoglobulin products
title_short High-resolution physicochemical characterization of different intravenous immunoglobulin products
title_sort high-resolution physicochemical characterization of different intravenous immunoglobulin products
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5536303/
https://www.ncbi.nlm.nih.gov/pubmed/28759653
http://dx.doi.org/10.1371/journal.pone.0181251
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