4.2 Article

Brief report: Production of anti-SARS-CoV-2 hyperimmune globulin from convalescent plasma

期刊

TRANSFUSION
卷 61, 期 6, 页码 1705-1709

出版社

WILEY
DOI: 10.1111/trf.16378

关键词

convalescent plasma; COVID-19; COVID-19 convalescent hyperimmune; hIVIG; immune globulin

资金

  1. Grifols Bioscience Research Group from the Bioscience Industrial Group, Research Triangle Park, NC, United States
  2. Grifols Therapeutics LLC, Clayton, NC, United States
  3. U S Biomedical Advanced Research and Development Authority (BARDA)

向作者/读者索取更多资源

This study utilized convalescent plasma to manufacture anti-SARS-CoV-2 hyperimmune globulin (hIVIG) with high purity and concentrated antibody activity, potentially serving as an effective treatment for COVID-19.
Background In late 2019, the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) virus emerged in China and quickly spread into a worldwide pandemic. Prior to the development of specific drug therapies or a vaccine, more immediately available treatments were sought including convalescent plasma. A potential improvement from convalescent plasma could be the preparation of anti-SARS-CoV-2 hyperimmune globulin (hIVIG). Study Design and Methods Convalescent plasma was collected from an existing network of plasma donation centers. A caprylate/chromatography purification process was used to manufacture hIVIG. Initial batches of hIVIG were manufactured in a versatile, small-scale facility designed and built to rapidly address emerging infectious diseases. Results Processing convalescent plasma into hIVIG resulted in a highly purified immunoglobulin G (IgG) product with more concentrated neutralizing antibody activity. hIVIG will allow for the administration of greater antibody activity per unit of volume with decreased potential for several adverse events associated with plasma administration. IgG concentration and IgG specific to SARS-CoV-2 were increased over 10-fold from convalescent plasma to the final product. Normalized enzyme-linked immunosorbent assay activity (per mg/ml IgG) was maintained throughout the process. Protein content in these final product batches was 100% IgG, consisting of 98% monomer and dimer forms. Potentially hazardous proteins (IgM, IgA, and anti-A, anti-B, and anti-D) were reduced to minimal levels. Conclusions Multiple batches of anti-SARS-CoV-2 hIVIG that met regulatory requirements were manufactured from human convalescent plasma. The first clinical study in which the hIVIG will be evaluated will be Inpatient Treatment with Anti-Coronavirus Immunoglobulin (ITAC) [NCT04546581].

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