Persistence of long-term immunity to hepatitis B among adolescents immunized at birth

被引:48
作者
Chaves, Sandra S. [1 ]
Fischer, Gayle [1 ]
Groeger, Justina [1 ]
Patel, Priti R. [1 ]
Thompson, Nicola D. [1 ]
Teshale, Eyasu H. [1 ]
Stevenson, Kuartei [2 ]
Yano, Victor M. [2 ]
Armstrong, Gregory L. [1 ]
Samandari, Taraz [1 ]
Kamili, Saleem [1 ]
Drobeniuc, Jan [1 ]
Hu, Dale J. [1 ]
机构
[1] Ctr Dis Control & Prevent, Atlanta, GA 30333 USA
[2] Minist Hlth, Koror, Palau
关键词
Anamnestic response; Hepatitis B vaccination; Hepatitis B virus; Long term immunity; VIRUS-INFECTION; HEPATOCELLULAR-CARCINOMA; FOLLOW-UP; ANAMNESTIC RESPONSE; VACCINATION; CHILDREN; TAIWAN; PROTECTION; INFANTS; DISEASE;
D O I
10.1016/j.vaccine.2011.12.106
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The long-term duration of recombinant hepatitis B vaccine-induced immunity among persons vaccinated starting at birth is still not well understood. Waning of vaccine-induced immunity could leave young adults at risk of hepatitis B virus infection due to behavioral or occupational exposures. We followed a cohort of children immunized starting at birth with a 3-dose regimen of recombinant hepatitis B vaccine (5 mcg, 2.5 mcg, 2.5 mcg). They were challenged with a booster dose of the hepatitis B vaccine 10 and 15 years after vaccination to assess anamnestic response as a measure of persistence of protection. Among 108 participants who had lost protective antibody levels against hepatitis B. the majority (>70%) had an anamnestic response to the booster dose; response rates did not decline significantly between 10 and 15 years follow-up periods. A high antibody concentration following primary vaccination was independently associated with an anamnestic response later on in life. Nonetheless, similar to 20-30% of participants were unable to mount an immune response after boosting. Hepatitis B revaccination might be required for persons vaccinated starting at birth if opportunities for hepatitis B virus exposure exist. Future vaccine recommendations should be based on studies ascertaining protection against clinically significant disease. Published by Elsevier Ltd.
引用
收藏
页码:1644 / 1649
页数:6
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