Das Kunal, Gupta R K, Kumar V, Kar P
Professor of Medicine, Maulana Azad Medical College & L.N. Hospital, New Delhi-110002, India.
World J Gastroenterol. 2003 May;9(5):1132-4. doi: 10.3748/wjg.v9.i5.1132.
The study was initiated to evaluate the reactogenicity and immunogenicity of a recombinant hepatitis B vaccine in age group >40 years and to study the response of a single booster dose in primary non-responders to the hepatitis B vaccination.
A total of 102 volunteers without markers of hepatitis B infection (negative for HBsAg, anti-HBc antibody, HBeAg and anti-HBs antibody) received 20 microg of recombinant HB vaccine intramuscularly at 0, 1, and 6 months. Anti HBs titers were evaluated by a quantitative Elisa kit at 90 and 210 days. A booster dose of 20 microg HB vaccine was given after 6 months of the 3(rd) vaccine dose to the 15 non-responders and anti-HBs titers were measured after 1 month.
Seroprotection (anti-HBs GMT(3) 10 IU/L) was achieved in 85.3 % (87/102) volunteers. The mean GMT titers of the vaccine responders was 136.1 IU/L. Of the seroprotected individuals, there were 32.4 % (33/102) hyporesponders (anti-HBs titers <10-99 mlU/ml) and 52.9 % (54/102) were responders (anti-HBs titers >100 IU/L). All the non-responders (15/15) responded to a single dose of the booster dose of recombinant HB vaccine and their mean anti-HBs antibody titers were more than 100.5 mIU/ml after the booster dose.
Recombinant hepatitis B vaccine offers good seroprotection in the age group >40 years and has a good safety profile. A single booster dose after 6 months in primary non-responders leads to good seroprotective anti-HBs antibody titers. However, larger population based studies are needed to evaluate the role of a booster dose in selected group of non-responders and whether such an approach will be cost effective.
开展本研究以评估重组乙型肝炎疫苗在40岁以上年龄组中的反应原性和免疫原性,并研究初次接种无应答者对乙肝疫苗单剂加强免疫的反应。
总共102名无乙肝感染标志物(乙肝表面抗原、抗乙肝核心抗体、乙肝e抗原和乙肝表面抗体均为阴性)的志愿者在0、1和6个月时肌肉注射20微克重组乙肝疫苗。在第90天和第210天通过定量酶联免疫吸附测定试剂盒评估乙肝表面抗体滴度。在第3剂疫苗接种6个月后,给15名无应答者接种一剂20微克的乙肝疫苗加强针,并在1个月后测量乙肝表面抗体滴度。
85.3%(87/102)的志愿者实现了血清保护(抗乙肝表面抗体几何平均滴度≥10 IU/L)。疫苗应答者的平均几何平均滴度为136.1 IU/L。在血清保护的个体中,32.4%(33/102)为低应答者(抗乙肝表面抗体滴度<10 - 99 mIU/ml),52.9%(54/102)为应答者(抗乙肝表面抗体滴度>100 IU/L)。所有无应答者(15/15)对单剂重组乙肝疫苗加强针有反应,加强针接种后他们的平均抗乙肝表面抗体滴度超过100.5 mIU/ml。
重组乙型肝炎疫苗在40岁以上年龄组中提供了良好的血清保护,且具有良好的安全性。初次接种无应答者在6个月后接种单剂加强针可产生良好的血清保护性抗乙肝表面抗体滴度。然而,需要开展更大规模的基于人群的研究来评估加强针在特定无应答者群体中的作用以及这种方法是否具有成本效益。