High-resolution physicochemical characterization of different intravenous immunoglobulin products

抗体 计算生物学 静脉注射免疫球蛋白 免疫学 免疫球蛋白G 医学 化学 生物
作者
Nathaniel Washburn,Robin Meccariello,Shaohui Hu,Maurice Hains,Naveen Bhatnagar,Hetal Sarvaiya,B. M. L. Kapoor,John Schaeck,Ignacio Pino,Anthony M. Manning,Jonathan C. Lansing,Carlos J. Bosques
出处
期刊:PLOS ONE [Public Library of Science]
卷期号:12 (7): e0181251-e0181251 被引量:7
标识
DOI:10.1371/journal.pone.0181251
摘要

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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