dc.contributor.author
Dähnert, Lisa
dc.contributor.author
Schlosser, Josephine
dc.contributor.author
Fast, Christine
dc.contributor.author
Fröhlich, Andreas
dc.contributor.author
Gröner, Albrecht
dc.contributor.author
Lange, Elke
dc.contributor.author
Roth, Nathan J.
dc.contributor.author
Schäfer, Wolfram
dc.contributor.author
Schröder, Charlotte
dc.contributor.author
Eiden, Martin
dc.date.accessioned
2021-04-09T07:36:21Z
dc.date.available
2021-04-09T07:36:21Z
dc.identifier.uri
https://refubium.fu-berlin.de/handle/fub188/30266
dc.identifier.uri
http://dx.doi.org/10.17169/refubium-30007
dc.description.abstract
Background Hepatitis E virus (HEV) is the leading cause of acute hepatitis throughout the world. Increasing blood component transfusion-associated HEV infections highlight the need for reliable virus inactivation procedures for plasma derivatives from pooled plasma donations.
Study Design and Methods An animal infection study was conducted to evaluate the efficiency of HEV inactivation by pasteurization during the manufacturing process of the von Willebrand Factor/Factor VIII (VWF/FVIII) concentrate Haemate P/Humate-P (CSL Behring, Marburg, Germany). For this purpose, groups of pigs were inoculated with stabilized VWF/FVIII intermediate spiked with HEV-positive liver homogenate and exposed to increasing incubation times of 0, 3, 6, and 10 h at 60 degrees C. Animals were evaluated for virus replication over 27 days and in a subsequent trial over 92 days.
Results Virus replication was detected in animals up to the 6-h pasteurization group. In contrast, pasteurization for 10 h did not reveal virus detection when the observation period was 27 days. In an additional experiment using the 10-h pasteurized material, two individuals started virus excretion and seroconverted when the observation period was extended to 92 days. Based on the total infection rate (2 of 12) of the animals inoculated with the sample pasteurized for 10 h, a virus reduction factor of at least 4.7 log(10) is calculated.
Conclusion This study demonstrates that pasteurization at 60 degrees C for 10 h of an HEV-positive plasma derivative leads to the effective reduction of infectivity, resulting in a VWF/FVIII product with an appropriate margin of safety for HEV.
en
dc.format.extent
12 Seiten
dc.rights.uri
https://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subject
hepatitis E virus
en
dc.subject
inactivation
en
dc.subject
pasteurization
en
dc.subject
plasma product
en
dc.subject.ddc
500 Naturwissenschaften und Mathematik::570 Biowissenschaften; Biologie::570 Biowissenschaften; Biologie
dc.title
Hepatitis E virus: Efficacy of pasteurization of plasma‐derived VWF/FVIII concentrate determined by pig bioassay
dc.type
Wissenschaftlicher Artikel
dcterms.bibliographicCitation.doi
10.1111/trf.16298
dcterms.bibliographicCitation.journaltitle
Transfusion
dcterms.bibliographicCitation.number
4
dcterms.bibliographicCitation.pagestart
1266
dcterms.bibliographicCitation.pageend
1277
dcterms.bibliographicCitation.volume
61
dcterms.bibliographicCitation.url
https://doi.org/10.1111/trf.16298
refubium.affiliation
Veterinärmedizin
refubium.affiliation.other
Institut für Immunologie

refubium.resourceType.isindependentpub
no
dcterms.accessRights.openaire
open access
dcterms.isPartOf.eissn
1537-2995
refubium.resourceType.provider
WoS-Alert