Methylene Blue Treatment of Grafts During Cold Ischemia Time Reduces the Risk of Hepatitis C Virus Transmission.
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Authors
Helfritz, Fabian ABojkova, Denisa
Wanders, Verena
Kuklinski, Nina
Westhaus, Sandra
von Horn, Charlotte
Rauen, Ursula
Gallinat, Anja
Baba, Hideo A
Skyschally, Andreas
Swoboda, Sandra
Kinast, Volker
Steinmann, Eike
Heusch, Gerd
Minor, Thomas
Meuleman, Philip
Paul, Andreas
Ciesek, Sandra
Issue Date
2018-12-01
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Show full item recordAbstract
Background: Although organ shortage is a rising problem, organs from hepatitis C virus (HCV) ribonucleic acid (RNA)-positive donors are not routinely transplanted in HCV-negative individuals. Because HCV only infects hepatocytes, other organs such as kidneys are merely contaminated with HCV via the blood. In this study, we established a protocol to reduce HCV virions during the cold ischemic time. Methods: Standard virological assays were used to investigate the effect of antivirals, including methylene blue (MB), in different preservation solutions. Kidneys from mini pigs were contaminated with Jc1 or HCV RNA-positive human serum. Afterwards, organs were flushed with MB. Hypothermic machine perfusion was used to optimize reduction of HCV. Results: Three different antivirals were investigated for their ability to inactivate HCV in vitro. Only MB completely inactivated HCV in the presence of all perfusion solutions. Hepatitis C virus-contaminated kidneys from mini pigs were treated with MB and hypothermic machine perfusion without any negative effect on the graft. Human liver-uPA-SCID mice did not establish HCV infection after inoculation with flow through from these kidneys. Conclusions: This proof-of-concept study is a first step to reduce transmission of infectious HCV particles in the transplant setting and might serve as a model for other relevant pathogens.Citation
J Infect Dis. 2018;218(11):1711-1721. doi:10.1093/infdis/jiy386.Affiliation
TWINCORE, Zentrum für experimentelle und klinische Infektionsforschung GmbH,Feodor-Lynen Str. 7, 30625 Hannover, Germany.Publisher
Oxford AcademicPubMed ID
29939277Type
ArticleLanguage
enEISSN
1537-6613ae974a485f413a2113503eed53cd6c53
10.1093/infdis/jiy386
Scopus Count
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