Dr PATRICK MCCLURE PATRICK.MCCLURE@NOTTINGHAM.AC.UK
ASSISTANT PROFESSOR
Reconstruction of the historic time course of blood‐borne virus contamination of clotting factor concentrates, 1974–1992
McClure, C. Patrick; Kean, Kai; Reid, Kaitlin; Mayne, Richard; Fu, Michael X.; Rajendra, Piya; Gates, Shannah; Breuer, Judy; Harvala, Heli; Golubchik, Tanya; Tarr, Alexander W.; Irving, William L.; Makris, Michael; Simmonds, Peter
Authors
Kai Kean
Kaitlin Reid
Richard Mayne
Michael X. Fu
Piya Rajendra
Shannah Gates
Judy Breuer
Heli Harvala
Tanya Golubchik
Dr ALEXANDER TARR alex.tarr@nottingham.ac.uk
ASSOCIATE PROFESSOR
William L. Irving
Michael Makris
Peter Simmonds
Abstract
Factor VIII and IX clotting factor concentrates manufactured from pooled plasma have been identified as potent sources of virus infection in persons with hemophilia (PWHs) in the 1970s and 1980s. To investigate the range and diversity of viruses over this period, we analysed 24 clotting factor concentrates for several blood-borne viruses. Nucleic acid was extracted from 14 commercially produced clotting factors and 10 from nonremunerated donors, preserved in lyophilized form (expiry dates: 1974–1992). Clotting factors were tested by commercial and in-house quantitative PCRs for blood-borne viruses hepatitis A, B, C and E viruses (HAV, HBV, HCV, HEV), HIV- types 1/2, parvoviruses B19V and PARV4, and human pegiviruses types 1 and 2 (HPgV-1,-2). HCV and HPgV-1 were the most frequently detected viruses (both 14/24 tested) primarily in commercial clotting factors, with frequently extremely high viral loads in the late 1970s–1985 and a diverse range of HCV genotypes. Detection frequencies sharply declined following introduction of virus inactivation. HIV-1, HBV, and HAV were less frequently detected (3/24, 1/24, and 1/24 respectively); none were positive for HEV. Contrastingly, B19V and PARV4 were detected throughout the study period, even after introduction of dry heat treatment, consistent with ongoing documented transmission to PWHs into the early 1990s. While hemophilia treatment is now largely based on recombinant factor VIII/IX in the UK and elsewhere, the comprehensive screen of historical plasma-derived clotting factors reveals extensive exposure of PWHs to blood-borne viruses throughout 1970s-early 1990s, and the epidemiological and manufacturing parameters that influenced clotting factor contamination.
Citation
McClure, C. P., Kean, K., Reid, K., Mayne, R., Fu, M. X., Rajendra, P., Gates, S., Breuer, J., Harvala, H., Golubchik, T., Tarr, A. W., Irving, W. L., Makris, M., & Simmonds, P. (2024). Reconstruction of the historic time course of blood‐borne virus contamination of clotting factor concentrates, 1974–1992. Journal of Medical Virology, 96(7), Article e29774. https://doi.org/10.1002/jmv.29774
Journal Article Type | Article |
---|---|
Acceptance Date | Jun 21, 2024 |
Online Publication Date | Jul 2, 2024 |
Publication Date | 2024-07 |
Deposit Date | Jul 12, 2024 |
Publicly Available Date | Jul 12, 2024 |
Journal | Journal of Medical Virology |
Print ISSN | 0146-6615 |
Electronic ISSN | 1096-9071 |
Publisher | Wiley |
Peer Reviewed | Peer Reviewed |
Volume | 96 |
Issue | 7 |
Article Number | e29774 |
DOI | https://doi.org/10.1002/jmv.29774 |
Keywords | clotting factor; Factor IX; Factor VIII; hemophilia; hepatitis A virus; hepatitis B virus; HIV-1; human pegivirus; PARV4; parvovirus B19 |
Public URL | https://nottingham-repository.worktribe.com/output/36877160 |
Publisher URL | https://onlinelibrary.wiley.com/doi/10.1002/jmv.29774 |
PMID | 38953434 |
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