scholarly journals Clarification to Long-term anti-HBs antibody persistence and immune memory in children and adolescents who received routine childhood hepatitis B vaccination. Hum Vaccin Immunother 2012; 8:813-8

2012 ◽  
Vol 8 (6) ◽  
pp. 813-818 ◽  
Author(s):  
Ulrich Behre ◽  
Gerhard Bleckmann ◽  
Priya Diana Crasta ◽  
Maarten Leyssen ◽  
Marc Messier ◽  
...  
Vaccine ◽  
2012 ◽  
Vol 30 (32) ◽  
pp. 4757-4761 ◽  
Author(s):  
Tessa Braeckman ◽  
Koen Van Herck ◽  
Wolfgang Jilg ◽  
Tanja Bauer ◽  
Pierre Van Damme

Vaccine ◽  
2011 ◽  
Vol 29 (5) ◽  
pp. 1005-1008 ◽  
Author(s):  
F. Zingone ◽  
F. Morisco ◽  
A. Zanetti ◽  
L. Romanò ◽  
G. Portella ◽  
...  

Infection ◽  
2011 ◽  
Vol 40 (3) ◽  
pp. 299-302 ◽  
Author(s):  
T. Stroffolini ◽  
◽  
V. Guadagnino ◽  
B. Caroleo ◽  
G. De Sarro ◽  
...  

Vaccine ◽  
1994 ◽  
Vol 12 (11) ◽  
pp. 978-983 ◽  
Author(s):  
D. Pillay ◽  
C. Pereira ◽  
C. Sabin ◽  
L. Powell ◽  
A.J. Zuckerman ◽  
...  

2021 ◽  
Author(s):  
Juan Wang ◽  
Chang-Hai Liu ◽  
Yuanji Ma ◽  
Xia Zhu ◽  
Liru Luo ◽  
...  

Abstract Background: The short-term 0-1-2-months hepatitis B virus (HBV) vaccination schedule was previously proposed in the adult population; however, its long-term immune effect remains unclear. The present study was aimed to investigate 1) the 2-months and 2-year immune effect of HBV vaccination; and 2) compliance rate between 0-1-2-months and 0-1-6-months vaccination schedules in adults.Method: A total of 1281 subjects tested for HBsAg(-) and Hepatitis B surface antibody (anti-HBs)(-) were recruited. Participants from two distant counties were inoculated hepatitis B yeast vaccine for 10ug per dose each time, with 0-1-2-months (n=606) and 0-1-6-months (n=675) vaccination schedule, sequentially followed-up at two months and two years after the 3rd injection.Results: There was no statistical difference in anti-HBs seroconversion rate between 0-1-2-months and 0-1-6-months vaccination schedule at two months (91.96% vs 89.42%, p=0.229) and two years (81.06% vs. 77.14%, p=0.217). Quantitative anti-HBs level of 0-1-2-months vaccination schedule was not different with 0-1-6-months vaccination schedule at 2 months (anti-HBs1) (342.12 ± 378.42 m IU/ml vs. 392.38 ± 391.96 m IU/ml, p=0.062), but was higher at two years (anti-HBs2) (198.37 ± 286.44 m IU /ml vs. 155.65 ± 271.73 m IU /ml, p=0.048). By subgroup analysis, 0-1-2-months vaccination schedule showed better maintenance (p=0.041) and delayed reinforcement (p=0.019) in comparison to 0-1-6 vaccination schedule. The 0-1-2-months vaccination schedule also increased the 3rd-time injection completion rate (89.49% vs. 84.49%, p=0.010).Conclusion: the 0-1-2-months vaccination could obtain a similar short-term immune effect, but achieve a better long-term immune memory and a higher completion rate in the adult population.Trial registration: None


Vaccines ◽  
2020 ◽  
Vol 8 (3) ◽  
pp. 456
Author(s):  
Takako Inoue ◽  
Yasuhito Tanaka

Hepatitis B (HB) vaccination is the most effective method for preventing HB virus (HBV) infection. Universal HB vaccination containing recombinant HB surface antigens (HBsAg) is recommended. Our data revealed that human monoclonal HB surface antibody (anti-HBs) from individuals inoculated with genotype C-based HB vaccine induced cross-protection against HBV genotype A infection. An in vitro infection model demonstrated anti-HBs-positive sera from individuals inoculated with genotype A- or C-based HB vaccine harbored polyclonal anti-HBs that could bind to non-vaccinated genotype HBV. However, because there were low titers of anti-HBs specific for HBsAg of non-vaccinated genotype, high anti-HBs titers would be required to prevent non-vaccinated genotype HBV infection. Clinically, the 2015 Centers for Disease Control and Prevention guidelines state that periodic monitoring of anti-HBs levels after routine HB vaccination is not needed and that booster doses of HB vaccine are not recommended. However, the American Red Cross suggests that HB-vaccine-induced immune memory might be limited; although HB vaccination can prevent clinical liver injury (hepatitis), subclinical HBV infections of non-vaccinated genotypes resulting in detectable HB core antibody could not be completely prevented. Therefore, monitoring anti-HBs levels after routine vaccination might be necessary for certain subjects in high-risk groups.


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