Optimal titer of anti‐HBs in blood components derived from donors with anti‐HBc
Autor: | Masashi Mizokami, Keiji Matsubayashi, Masahiro Satake, Naoji Yamagishi, Takashi Hasegawa, Tadashi Nagai, Masaya Sugiyama, Shigeharu Uchida, Yuji Hoshi |
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Rok vydání: | 2019 |
Předmět: |
Adult
Male Anti hbs Hepatitis B virus Genotype Immunology Blood Component Transfusion Blood Donors Viremia 030204 cardiovascular system & hematology medicine.disease_cause Mice Plasma 03 medical and health sciences 0302 clinical medicine Japan Antigen medicine Animals Humans Immunology and Allergy Hepatitis B Antibodies Aged Severe combined immunodeficiency Hepatitis B Surface Antigens business.industry virus diseases Hematology Middle Aged medicine.disease Virology digestive system diseases Anti hbc Titer Female business 030215 immunology |
Zdroj: | Transfusion. 59:2602-2611 |
ISSN: | 1537-2995 0041-1132 |
DOI: | 10.1111/trf.15393 |
Popis: | BACKGROUND The ultimate strategy to cope with transfusion-transmitted hepatitis B virus (HBV) infection caused by transfusion of blood from donors with historical HBV infection is to reject all donors having anti-HBV core antigen (anti-HBc). However, this strategy would result in a huge loss of blood donors and subsequent blood inventory collapse. On the other hand, anti-HBc-positive blood is reportedly not infectious when containing more than 100 mIU/mL of anti-HBV surface antigen (anti-HBs). STUDY DESIGN AND METHODS In Japan, anti-HBc-positive blood has been used for transfusion if it contained 200 mIU/mL or more of anti-HBs. First, to verify the screening policy, clinical outcomes for transfusion of such blood were analyzed for the 2008-2012 period. Second, human hepatocyte-repopulated severe combined immunodeficiency mice were inoculated with HBV preincubated with varying doses of anti-HBs, then viremic status was followed. The effects of anti-HBs across different HBV genotypes were also investigated. RESULTS Twenty-three transfusion-transmitted HBV infections related to anti-HBc-positive blood components were identified. None of the blood responsible for these cases contained 200 mIU/mL or more of anti-HBs. When 100 μL of plasma containing 104 copies of HBV and 20 mIU of anti-HBs was injected into severe combined immunodeficiency mice, no viremia was detected within 13 weeks. Genotype C anti-HBs was capable of total inhibition of genotype A HBV replication, whereas genotype A anti-HBs inhibited genotype C HBV to a lesser extent. CONCLUSION Anti-HBc-positive blood containing 200 mIU/mL or more of anti-HBs appears safe as a transfusion component. HBV vaccination seems effective between HBV genotypes A and C. |
Databáze: | OpenAIRE |
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