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Two-center validation of assays for the detection of binding and neutralizing anti-factor VIII antibodies.

Authors :
Müller J
Neimanis S
Kahle J
Albert T
Schultze Strasser S
Rup B
Pötzsch B
Königs C
Oldenburg J
Source :
Haemophilia : the official journal of the World Federation of Hemophilia [Haemophilia] 2024 Jan; Vol. 30 (1), pp. 224-231. Date of Electronic Publication: 2023 Oct 12.
Publication Year :
2024

Abstract

Introduction: Patients with hemophilia A treated with coagulation Factor VIII (FVIII) products are at risk for developing anti-FVIII antibodies. The ABIRISK Consortium aimed to provide knowledge on the formation and detection of anti-drug antibodies against biopharmaceutical products, including FVIII. Accordingly, standardized and validated assays for the detection of binding (total) and neutralizing antibodies are needed.<br />Aim: Two-center validation of an ELISA for the detection of total FVIII-binding IgG-antibodies and Nijmegen-Bethesda assays for the quantification of FVIII-neutralizing antibodies according to consensus validation guidelines.<br />Methods: Validation of assays at both sites was done according to published recommendations and included preanalytics, the determination of key assay parameters, including cut-points, assay sensitivity, precision, and FVIII interference.<br />Results: The validated assays reproducibly detected FVIII-binding and -neutralizing antibodies with comparable performance in both laboratories. Floating screening cut-points were established for both assays. Determined mass-based sensitivity of both assays (all values ≤66 ng/mL) complied with the minimum sensitivity for the detection of anti-drug antibodies as recommended by the FDA (<100 ng/mL). Intra- and inter-assay coefficients of variation did not exceed 25%. Assay validation further revealed that pre-analytical heat treatment led to potentially false-positive ELISA results, while up to 0.15 IU/mL, residual FVIII showed no significant impact. Overall, good agreement of results was found for patient samples analyzed at both study sites.<br />Conclusion: Comprehensive validation of different anti-FVIII-antibody assays in two laboratories gave novel insights into the impact of pre-analytical sample treatment as well as the comparability of test results generated by the use of methodically different assays.<br /> (© 2023 The Authors. Haemophilia published by John Wiley & Sons Ltd.)

Details

Language :
English
ISSN :
1365-2516
Volume :
30
Issue :
1
Database :
MEDLINE
Journal :
Haemophilia : the official journal of the World Federation of Hemophilia
Publication Type :
Academic Journal
Accession number :
37824540
Full Text :
https://doi.org/10.1111/hae.14885