Incidences of new hepatitis B infection and anti-hepatitis B core-negative occult hepatitis B infection among Japanese blood donors in relation to anti-hepatitis B surface antigen levels.


Journal

Journal of medical virology
ISSN: 1096-9071
Titre abrégé: J Med Virol
Pays: United States
ID NLM: 7705876

Informations de publication

Date de publication:
Jul 2024
Historique:
revised: 05 07 2024
received: 08 04 2024
accepted: 15 07 2024
medline: 23 7 2024
pubmed: 23 7 2024
entrez: 23 7 2024
Statut: ppublish

Résumé

A transfusion-transmitted hepatitis B virus (HBV) infection caused by blood only positive for anti-hepatitis B surface antigen (anti-HBs) was reported. Occult HBV infection (OBI) with sole anti-HBs among blood donors is an issue. The incidence of HBV infection among repeat blood donors was investigated with a detailed HBV infection phase, focusing on the influence of anti-HBs level. This study followed 3 435 653 donors for HBV DNA conversion over 4 years and 9 months. Infection phase was determined based on marker changes over DNA conversion. This study identified 115 hepatitis B surface antigen (HBsAg) conversions, 72 DNA-only conversions, and 15 DNA plus anti-hepatitis B core (anti-HBc) conversions among donors all negative for HBV DNA, HBsAg, and anti-HBc. Total incidence was 2.38/100 000 person-years (PY). None of these 202 new HBV infections arose in the group with anti-HBs titer ≥ 10 mIU/mL. In total, 30 anti-HBc-negative OBIs were identified (incidence; 0.35/100 000 PY); 7 showed typical secondary anti-HBs response, and 23 showed stable anti-HBc and anti-HBs levels at DNA conversion. The HBV infection-protective ability of anti-HBs ≥ 10 mIU/mL was reinforced. In addition to new infections, the blood donor population includes anti-HBc-positive- and negative OBI with immune reactions or abortive HBV infection.

Identifiants

pubmed: 39039862
doi: 10.1002/jmv.29823
doi:

Substances chimiques

Hepatitis B Surface Antigens 0
Hepatitis B Antibodies 0
DNA, Viral 0
Hepatitis B Core Antigens 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e29823

Subventions

Organisme : Ministry of Health, Labour and Welfare, Japan
ID : 22HC1001

Informations de copyright

© 2024 Wiley Periodicals LLC.

Références

WHO Fact Sheet. Hepatitis B. Accessed December 2023. https://www.who.int/news-room/fact-sheets/detail/hepatitis-b
Tanaka J, Kumagai J, Katayama K, et al. Sex‐ and age‐specific carriers of hepatitis B and C viruses in Japan estimated by the prevalence in the 3,485,648 first‐time blood donors during 1995‐2000. Intervirology. 2004;47(1):32‐40.
Tanaka J, Koyama T, Mizui M, et al. Total numbers of undiagnosed carriers of hepatitis C and B viruses in Japan estimated by age‐ and area‐specific prevalence on the national scale. Intervirology. 2011;54(4):185‐195.
Tanaka J, Akita T, Ohisa M, et al. Trends in the total numbers of HBV and HCV carriers in Japan from 2000 to 2011. J Viral Hepat. 2018;25(4):363‐372.
Tanaka J, Kurisu A, Ohara M, et al. Burden of chronic hepatitis B and C infections in 2015 and future trends in Japan: a simulation study. Lancet Reg Health West Pac. 2022;22:100428.
Candotti D, Allain JP. Transfusion‐transmitted hepatitis B virus infection. J Hepatol. 2009;51(4):798‐809.
Lelie N, Busch M, Kleinman S. Residual risk of transfusion‐transmitted hepatitis B virus (TT‐HBV) infection by NAT‐screened blood components: a review of observed versus modeled infectivity from donors with window period and occult HBV infections. Transfusion. 2021;61(11):3190‐3201.
Tanaka A, Yamagishi N, Hasegawa T, et al. Marked reduction in the incidence of transfusion‐transmitted hepatitis B virus infection after the introduction of antibody to hepatitis B core antigen and individual donation nucleic acid amplification screening in Japan. Transfusion. 2023;63(11):2083‐2097.
Satake M, Yamagishi N, Tanaka A, et al. Transfusion‐transmitted HBV infection with isolated anti‐HBs‐positive blood. Transfusion. 2023;63(6):1250‐1254.
FitzSimons D, Hendrickx G, Vorsters A, Van Damme P. Hepatitis B vaccination: a completed schedule enough to control HBV lifelong? Vaccine. 2013;31(4):584‐590.
Katz L, Strong DM, Tegtmeier G, Stramer S. Performance of an algorithm for the reentry of volunteer blood donors deferred due to false‐positive test results for antibody to hepatitis B core antigen. Transfusion. 2008;48(11):2315‐2322.
Schmidt M, Nübling CM, Scheiblauer H, et al. Anti‐HBc screening of blood donors: a comparison of nine anti‐HBc tests. Vox Sang. 2006;91(3):237‐243.
Szmuness W, Stevens CE, Harley EJ, et al. Hepatitis B vaccine: demonstration of efficacy in a controlled clinical trial in a high‐risk population in the United States. N Engl J Med. 1980;303(15):833‐841.
Francis DP. The prevention of hepatitis B with vaccine. Report of the centers for disease control multi‐center efficacy trial among homosexual men. Ann Intern Med. 1982;97(3):362‐366.
Mast EE, Margolis HS, Fiore AE, et al. A comprehensive immunization strategy to eliminate transmission of hepatitis B virus infection in the United States: recommendations of the Advisory Committee on Immunization Practices (ACIP) part 1: immunization of infants, children, and adolescents. MMWR Recomm Rep. 2005;54(RR‐16):1‐31.
Pei SN, Liu YF, Kuo CY, et al. Role of quantitative hepatitis B surface antibodies in preventing hepatitis B virus‐related hepatitis in patients treated with rituximab. Leuk Lymphoma. 2021;62(12):2899‐2906.
Cho Y, Yu SJ, Cho EJ, et al. High titers of anti‐HBs prevent rituximab‐related viral reactivation in resolved hepatitis B patient with non‐Hodgkin's lymphoma. J Med Virol. 2016;88:1010‐1017.
Weber B. Genetic variability of the S gene of hepatitis B virus: clinical and diagnostic impact. J Clin Virol. 2005;32(2):102‐112.
Raimondo G, Pollicino T, Cacciola I, Squadrito G. Occult hepatitis B virus infection. J Hepatol. 2007;46(1):160‐170.
Shinkai N, Kusumoto S, Murakami S, et al. Novel monitoring of hepatitis B reactivation based on ultra‐high sensitive hepatitis B surface antigen assay. Liver Int. 2017;37(8):1138‐1147.
Matsumoto A, Imaizumi M, Tanaka Y, et al. Novel and highly sensitive immunoassay for total hepatitis B surface antigen, including that complexed with hepatitis B surface antibody. J Gastroenterol. 2017;52(3):376‐384.
Tang X, Allain JP, Wang H, et al. Incidence of hepatitis B virus infection in young Chinese blood donors born after mandatory implementation of neonatal hepatitis B vaccination nationwide. J Viral Hepat. 2018;25(9):1008‐1016.
Poovorawan Y, Chongsrisawat V, Theamboonlers A, Bock HL, Leyssen M, Jacquet JM. Persistence of antibodies and immune memory to hepatitis B vaccine 20 years after infant vaccination in Thailand. Vaccine. 2010;28(3):730‐736.
Zanetti AR, Mariano A, Romanò L, et al. Long‐term immunogenicity of hepatitis B vaccination and policy for booster: an Italian multicentre study. Lancet. 2005;366(9494):1379‐1384.
Chen Y, Lv H, Gu H, et al. The effects of different dosage levels of hepatitis B vaccine as booster on anti‐HBs‐negative children 5‐15 y after primary immunization; China, 2009‐2010. Hum Vaccin Immunother. 2014;10:498‐504.
Leuridan E, Van Damme P. Hepatitis B and the need for a booster dose. Clin Infect Dis. 2011;53:68‐75.
Poorolajal J, Hooshmand E. Booster dose vaccination for preventing hepatitis B. Cochrane Database Syst Rev. 2016;2016(6):CD008256.
Lelie N, Bruhn R, Busch M, et al. Detection of different categories of hepatitis B virus (HBV) infection in a multi‐regional study comparing the clinical sensitivity of hepatitis B surface antigen and HBV‐DNA testing. Transfusion. 2017;57(1):24‐35.
Simons BC, Spradling PR, Bruden DJT, et al. A longitudinal hepatitis B vaccine cohort demonstrates long‐lasting hepatitis B virus (HBV) cellular immunity despite loss of antibody against HBV surface antigen. J Infect Dis. 2016;214(2):273‐280.
Jarrosson L, Kolopp‐Sarda MN, Aguilar P, et al. Most humoral non‐responders to hepatitis B vaccines develop HBV‐specific cellular immune responses. Vaccine. 2004;22(27‐28):3789‐3796.
Bauer T, Jilg W. Hepatitis B surface antigen‐specific T and B cell memory in individuals who had lost protective antibodies after hepatitis B vaccination. Vaccine. 2006;24(5):572‐577.
Steiner M, Ramakrishnan G, Gartner B, Van Der Meeren O, Jacquet JM, Schuster V. Lasting immune memory against hepatitis B in children after primary immunization with 4 doses of DTPa‐HBV‐IPV/Hib in the first and 2nd year of life. BMC Infect Dis. 2010;10:9.
Deng X, Guo X, Gu H, et al. Anti‐HBc‐nonreactive occult hepatitis B infections with HBV genotypes B and C in vaccinated immunocompetent adults. J Viral Hepat. 2022;29(11):958‐967.
Keating SM, Heitman JD, Wu S, et al. Cytokine and chemokine responses in the acute phase of hepatitis B virus replication in naive and previously vaccinated blood and plasma donors. J Infect Dis. 2014;209(6):845‐854.
Zheng X, Ye X, Du P, et al. High prevalence of anti‐hepatitis B core antigen in hepatitis B virus‐vaccinated Chinese blood donors suggests insufficient protection but little threat to the blood supply. Transfusion. 2015;55(4):890‐897.
Su FH, Bai CH, Chu FY, Lin YS, Su CT, Yeh CC. Significance and anamnestic response in isolated hepatitis B core antibody‐positive individuals 18 years after neonatal hepatitis B virus vaccination in Taiwan. Vaccine. 2012;30(27):4034‐4039.
Bulkow LR, Wainwright RB, Bulkow LR, Wainwright RB, McMahon BJ, Parkinson AJ. Increases in levels of antibody to hepatitis B surface antigen in an immunized population. Clin Infect Dis. 1998;26(4):933‐937.
Gessoni G, Beggio S, Barin P, et al. Significance of anti‐HBc only in blood donors: a serological and virological study after hepatitis B vaccination. Blood Transfus. 2014;12(suppl 1):s63‐s68.
Inaba S, Ito A, Miyata Y, et al. Individual nucleic amplification technology does not prevent all hepatitis B virus transmission by blood transfusion. Transfusion. 2006;46(11):2028‐2029.
Candotti D, Lin CK, Belkhiri D, et al. Occult hepatitis B infection in blood donors from South East Asia: molecular characterisation and potential mechanisms of occurrence. Gut. 2012;61(12):1744‐1753.
Wu D, Wang X, Feng F, et al. Characteristic of HBV nucleic acid amplification testing yields from blood donors in China. BMC Infect Dis. 2021;21(1):714.

Auteurs

Masahiro Satake (M)

Blood Service Headquarters, Japanese Red Cross, Tokyo, Japan.

Masaya Sugiyama (M)

Department of Viral Pathogenesis and Controls, National Center for Global Health and Medicine, Tokyo, Japan.

Masashi Mizokami (M)

Genome Medical Sciences Project, National Center for Global Health and Medicine, Tokyo, Japan.

Junko Tanaka (J)

Department of Epidemiology, Infectious Disease Control and Prevention, Graduate School of Biomedical and Health Sciences, Hiroshima University, Hiroshima, Japan.

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