Hospital de Niños Ricardo Gutierrez, Epidemiología, Buenos Aires, Argentina.
Int J Infect Dis. 2011 Jan;15(1):e24-9. doi: 10.1016/j.ijid.2010.09.004. Epub 2010 Nov 18.
In this open-label, non-randomized phase II study, the safety and immunogenicity of a fully liquid diphtheria-tetanus-whole cell pertussis-hepatitis B-Haemophilus influenzae type b (DTPw-HepB-Hib) combination vaccine (Quinvaxem(®)) were assessed in infants who had or had not received a birth dose of hepatitis B (HepB) vaccine.
Two groups of infants, 'HepB at birth' (n=110) and 'no HepB at birth' (n=108), were enrolled and received a primary vaccination course using a 2-4-6 months schedule.
Seroprotection/seroconversion rates of >95% were achieved against all antigens included in the combination vaccine for both study groups. Although significantly higher anti-hepatitis B virus (p<0.001) and anti-tetanus (p=0.031) antibody titers were achieved in group 'HepB at birth' when compared with group 'no HepB at birth', the proportion of 'no HepB at birth' subjects achieving protective titers was non-inferior to the proportion of subjects in group 'HepB at birth'. The birth dose of HepB vaccine did not seem to influence the safety pattern of the DTPw-HepB-Hib combination vaccine.
The present study demonstrated that the fully liquid DTPw-HepB-Hib vaccine was safe and immunogenic when administered using a 2-4-6 months immunization schedule, regardless of whether or not infants had received a dose of HepB vaccine at birth.
在这项开放标签、非随机的 2 期研究中,评估了一种全液体白喉-破伤风-全细胞百日咳-乙型肝炎-流感嗜血杆菌(DTPw-HepB-Hib)联合疫苗(Quinvaxem(®))在已接种或未接种乙型肝炎(HepB)疫苗出生剂量的婴儿中的安全性和免疫原性。
两组婴儿,“出生时接种 HepB”(n=110)和“出生时未接种 HepB”(n=108),按 2-4-6 个月的时间表接受了初级疫苗接种。
两组均对联合疫苗中包含的所有抗原达到了 >95%的保护/血清转化率。尽管与“出生时未接种 HepB”组相比,“出生时接种 HepB”组的乙型肝炎病毒(p<0.001)和破伤风(p=0.031)抗体滴度明显更高,但“出生时未接种 HepB”组达到保护滴度的比例与“出生时接种 HepB”组的比例相当。出生时接种 HepB 疫苗似乎并未影响 DTPw-HepB-Hib 联合疫苗的安全性模式。
本研究表明,全液体 DTPw-HepB-Hib 疫苗在按照 2-4-6 个月的免疫接种时间表接种时是安全且具有免疫原性的,无论婴儿出生时是否接种了 HepB 疫苗。