Volume 55, Issue S2 pp. S95-S97
IMMUNE GLOBULIN MANUFACTURING AND RISK MITIGATION

Donor screening reduces the isoagglutinin titer in immunoglobulin products

Brigitte Siani

Corresponding Author

Brigitte Siani

Biochemical Quality Control, Berne, Switzerland

Address reprint requests to: Brigitte Siani, CSL Behring AG, Wankdorfstrasse 10, 3000 Berne, Switzerland; e-mail: [email protected].Search for more papers by this author
Katharina Willimann

Katharina Willimann

Biochemical Quality Control, Berne, Switzerland

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Sandra Wymann

Sandra Wymann

Product Development, CSL Behring AG, Berne, Switzerland

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Adriano Marques Antunes

Adriano Marques Antunes

Biochemical Quality Control, Berne, Switzerland

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Eleonora Widmer

Eleonora Widmer

Biochemical Quality Control, Berne, Switzerland

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First published: 14 July 2015
Citations: 10

Abstract

BACKGROUND

Hemolysis reaction is a rare class effect of therapy with intravenously administered human normal immunoglobulin (IVIG). Anti-A/B isoagglutinins (isohemagglutinins) originating from donor plasma are considered a probable risk factor for hemolysis. We hypothesized that screening and exclusion of plasma obtained from donors with high isoagglutinin titers from the manufacturing process would produce a meaningful reduction of anti-A/B isoagglutinin titers of the final IVIG product.

STUDY DESIGN AND METHODS

A donor screening method for anti-A isoagglutinins using an automated indirect agglutination test (IAT) in gel cards was developed. Industry-scale donor plasma pools and final IVIG product were prepared according to the manufacturing process of Privigen (human 10% liquid IVIG). Anti-A/B isoagglutinin levels were measured by IAT, direct agglutination test, and a flow cytometry–based assay.

RESULTS

Screening of plasma from 705 randomly selected donors identified 6.8% donors with high anti-A isoagglutinin titers in plasma. Exclusion of plasma from these donors resulted in a one-titer-step reduction of anti-A isoagglutinin in laboratory-scale pooled plasma. The same donor screening method applied to industry-scale production resulted in exclusion of 5.1% of donors and produced a one-titer-step reduction of both anti-A and anti-B isoagglutinin titers in the final IVIG product.

CONCLUSION

Anti-A/B isoagglutinin titers in IVIG products can be reduced on an industrial scale through implementation of anti-A donor screening, which may lower the risk of hemolysis after IVIG therapy.

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