Hla Khin Hla, Thein Saw Aung Myat, Aye Aye, Han Htay-Htay, Bock Hans L, David Marie-Pierre, Schuerman Lode
Pediatric Unit No. 2, Military Hospital, Dagon Township, Yangon, Myanmar.
Pediatr Infect Dis J. 2006 Aug;25(8):706-12. doi: 10.1097/01.inf.0000223488.80814.df.
Combined vaccines containing diphtheria-tetanus-pertussis whole-cell (DTPw), Haemophilus influenzae type b (Hib), and hepatitis-B vaccines are essential for the continuing success of vaccination programs in developing nations. This randomized, dose-ranging study assessed the immunogenicity and reactogenicity of primary and booster vaccination with pentavalent DTPw-HBV/Hib vaccines containing 10, 5 or 2.5 microg of polyribosylribitol phosphate (PRP) conjugated to tetanus toxoid (trials Hib-052/064).
Six hundred eighty infants were randomized to receive one of 5 vaccine combinations at 6, 10, and 14 weeks of age. Of these, 351 received the same vaccine at 15-24 months of age. The immune response was evaluated on blood samples collected 1 month after the 3-dose primary course and before and 6 weeks after the booster dose. Reactogenicity was assessed during a 4-day period after each vaccine dose using diary cards.
After primary vaccination, all subjects had seroprotective anti-PRP antibody concentrations (> or = 0.15 microg/mL) and > 95% had concentrations > or = 1.0 microg/mL, irrespective of the PRP dose administered. Anti-PRP antibody avidity after primary vaccination and antibody persistence until the second year of life were similar among groups. The booster dose induced marked increases in anti-PRP antibody GMCs and antibody avidity, indicative of effective priming and the presence of immune memory. All vaccination regimens elicited good immune responses and comparable antibody persistence to the other vaccine antigens, with significant increases in all antibody concentrations observed after boosting. All vaccination regimens were safe, with similar overall reactogenicity profiles.
Hib conjugate vaccines containing reduced amounts of PRP can be effectively combined with the licensed DTPw-HBV vaccine to provide protection against 5 major childhood pathogens in a single injection.
含有白喉-破伤风-百日咳全细胞(DTPw)、b型流感嗜血杆菌(Hib)和乙型肝炎疫苗的联合疫苗对于发展中国家疫苗接种计划的持续成功至关重要。这项随机、剂量范围研究评估了含10、5或2.5微克与破伤风类毒素结合的多聚核糖基核糖醇磷酸酯(PRP)的五价DTPw-HBV/Hib疫苗进行初次和加强免疫接种的免疫原性和反应原性(试验Hib-052/064)。
680名婴儿在6、10和14周龄时随机接受5种疫苗组合之一。其中,351名在15至24月龄时接种相同疫苗。在3剂初次接种疗程后1个月、加强剂量前及加强剂量后6周采集的血样上评估免疫反应。使用日记卡,在每次疫苗接种后4天内评估反应原性。
初次接种后,所有受试者均有血清保护性抗PRP抗体浓度(≥0.15微克/毫升),且超过95%的受试者浓度≥1.0微克/毫升,无论所给予的PRP剂量如何。各年龄组初次接种后抗PRP抗体亲和力及直至生命第二年的抗体持久性相似。加强剂量使抗PRP抗体几何平均浓度(GMC)和抗体亲和力显著增加,表明有效启动及存在免疫记忆。所有疫苗接种方案均引发良好免疫反应及与其他疫苗抗原相当的抗体持久性,加强接种后所有抗体浓度均显著增加。所有疫苗接种方案均安全,总体反应原性概况相似。
含减少量PRP的Hib结合疫苗可有效与已获许可的DTPw-HBV疫苗联合,通过单次注射提供针对5种主要儿童期病原体的保护。