Pongpipat D, Suvatte V, Assateerawatts A
Department of Pediatrics, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand.
Asian Pac J Allergy Immunol. 1988 Dec;6(2):107-10.
A reduced dose of plasma derived hepatitis B vaccine (Hevac B) was tested for efficacy in the prevention of perinatal hepatitis B virus (HBV) transmission in high risk neonates born from e-antigen positive HBsAg carrier mothers. Forty newborn infants born of these mothers were given hepatitis B immune globulin (HBIG) 100 IU intramuscularly immediately after birth, combined with either standard or reduced doses of HBV vaccine. The infants were divided into two groups of 20 infants each. The standard dose of HBV vaccine (5 micrograms) was given to group I, while infants in group II received reduced dose (2 micrograms) at birth and at 1, 2 and 12 months of age. There was no statistically significant difference in the efficacy and antibody responses of these two combined prophylaxis regimens. The protective efficacy rate of HBV vaccine was found to be 94.0 and 93.2 percent in group I and group II, respectively. At twelve months of age, the anti-HBs seroconversion rates were 80.0 percent in group I and 86.7 percent in group II, with geometric mean titres of 84.57 mlU/ml and 78.56 mlU/ml, in group I and group II, respectively. One month after a booster at one year of age, anti-HBs could be detected in 86.7 percent of the infants in both groups. The geometric mean titres were 429.04 and 664.81 mlU/ml, in group I and group II, respectively. Anti-PreS2 antibody was detected in high titre as early as 4 months after the first dose of HBV vaccine, with a geometric mean titre of 116.30 mlU/ml and 107.97 mlU/ml, in group I and group II, respectively.(ABSTRACT TRUNCATED AT 250 WORDS)
对一种剂量减少的血浆源性乙肝疫苗(Hevac B)进行了测试,以评估其在预防由e抗原阳性HBsAg携带者母亲所生高危新生儿围产期乙肝病毒(HBV)传播方面的疗效。这些母亲所生的40名新生儿在出生后立即肌肉注射100 IU乙肝免疫球蛋白(HBIG),并同时接种标准剂量或减少剂量的乙肝疫苗。婴儿被分为两组,每组20名。第一组接种标准剂量的乙肝疫苗(5微克),而第二组婴儿在出生时、1个月、2个月和12个月时接种减少剂量(2微克)。这两种联合预防方案在疗效和抗体反应方面没有统计学上的显著差异。发现乙肝疫苗在第一组和第二组中的保护有效率分别为94.0%和93.2%。在12个月大时,第一组的抗-HBs血清转化率为80.0%,第二组为86.7%,第一组和第二组的几何平均滴度分别为84.57 mlU/ml和78.56 mlU/ml。在1岁时加强免疫1个月后,两组中86.7%的婴儿都能检测到抗-HBs。第一组和第二组的几何平均滴度分别为429.04和664.81 mlU/ml。早在接种第一剂乙肝疫苗后4个月就检测到高滴度的抗-PreS2抗体,第一组和第二组的几何平均滴度分别为116.30 mlU/ml和107.97 mlU/ml。(摘要截断于250字)