Samandari Taraz, Fiore Anthony E, Negus Susan, Williams James L, Kuhnert Wendi, McMahon Brian J, Bell Beth P
Division of Viral Hepatitis, Centers for Disease Control and Prevention, Atlanta, GA 30333, USA.
Pediatrics. 2007 Aug;120(2):e373-81. doi: 10.1542/peds.2007-0131. Epub 2007 Jul 16.
The duration of protection provided by hepatitis B vaccination is unknown, but the presence of immune memory can be evaluated indirectly by measuring the immune response to a booster dose of vaccine.
Participants included 74 adolescents (aged 11.7-14.9 years) who had received a plasma-derived 3-dose primary vaccine series and 138 adolescents (aged 10.0-14.7 years) and 166 children (aged 5.0-7.0 years) who received a recombinant 3-dose primary vaccine series. All were born to hepatitis B surface antigen-negative mothers and had received the first dose of hepatitis B vaccine within 7 days of birth. The proportion of participants with serologic evidence of protective immunity (antibody to hepatitis B surface antigen > or = 10 mIU/mL) at baseline (prebooster), the proportion who developed an anamnestic response (increase to > or = 10 mIU/mL or at or more than fourfold increase in antibody to hepatitis B surface antigen to > 10 mIU/mL), and the geometric mean concentration by 1, 2, and 4 weeks after a 5-microg recombinant vaccine booster dose were determined.
No participant had evidence of chronic hepatitis B virus infection. Overall, 99% of the group of children who received recombinant hepatitis B vaccine, 83% of the group of adolescents who received recombinant hepatitis B vaccine, and 69% of the group of adolescents who received the plasma-derived vaccine had an anamnestic response to a booster dose; among responders, the geometric mean concentration at 2 weeks postbooster was 3360 and 128 mIU/mL among adolescents who received plasma-derived vaccine with antibodies to hepatitis B surface antigen > or = 10 and < 10 mIU/mL at baseline, respectively, compared with 1283 and 369 mIU/mL among adolescents who received recombinant hepatitis B vaccine and 5091 and 696 mIU/mL for children who received recombinant hepatitis B vaccine. The anamnestic response rate at 2 weeks postbooster among participants with antibodies to hepatitis B surface antigen < 10 mIU/mL at baseline was inversely associated with age; 97% of 5-year-olds responded compared with 60% of 14-year-olds.
Although most participants responded to a booster dose of hepatitis B vaccine, the significance of the increased proportion of nonresponses among older adolescents might indicate waning immune memory.
乙型肝炎疫苗提供的保护持续时间尚不清楚,但可通过测量对疫苗加强剂量的免疫反应间接评估免疫记忆的存在情况。
参与者包括74名接受过3剂血浆源性乙肝疫苗初免系列的青少年(年龄11.7 - 14.9岁),以及138名接受过3剂重组乙肝疫苗初免系列的青少年(年龄10.0 - 14.7岁)和166名儿童(年龄5.0 - 7.0岁)。所有儿童均为乙肝表面抗原阴性母亲所生,且在出生后7天内接种了第一剂乙肝疫苗。测定基线(加强免疫前)时具有保护性免疫血清学证据(乙肝表面抗原抗体>或=10 mIU/mL)的参与者比例、出现回忆反应(抗体增加至>或=10 mIU/mL,或乙肝表面抗原抗体增加至>10 mIU/mL且增加四倍或更多)的参与者比例,以及在5μg重组疫苗加强剂量后1周、2周和4周时的几何平均浓度。
无参与者有慢性乙肝病毒感染证据。总体而言,接受重组乙肝疫苗的儿童组中99%、接受重组乙肝疫苗的青少年组中83%、接受血浆源性疫苗的青少年组中69%对加强剂量有回忆反应;在有反应者中,加强免疫后2周时,基线时乙肝表面抗原抗体>或=10 mIU/mL和<10 mIU/mL的接受血浆源性疫苗的青少年的几何平均浓度分别为3360和128 mIU/mL,接受重组乙肝疫苗的青少年分别为1283和369 mIU/mL,接受重组乙肝疫苗的儿童分别为5091和696 mIU/mL。基线时乙肝表面抗原抗体<10 mIU/mL的参与者在加强免疫后2周时的回忆反应率与年龄呈负相关;5岁儿童中有97%有反应,而14岁儿童中为60%。
虽然大多数参与者对乙肝疫苗加强剂量有反应,但年龄较大青少年中无反应比例增加的意义可能表明免疫记忆在减弱。