Punjabi Narain H, Richie Emily L, Simanjuntak Cyrus H, Harjanto Sri Juliani, Wangsasaputra Ferry, Arjoso Sumarjati, Rofiq Ainur, Prijanto Mulyati, Yela Ursula, Herzog Christian, Cryz Stanley J
U.S. Naval Medical Research Unit No. 2, Jakarta, Indonesia.
Vaccine. 2006 Mar 10;24(11):1776-85. doi: 10.1016/j.vaccine.2005.10.023. Epub 2005 Oct 27.
Widespread use of Haemophilus influenzae type b (Hib) conjugated vaccine in industrialized countries has resulted in a dramatic decline in the incidence of invasive Hib diseases, but the vaccine's cost has prevented its inclusion in basic immunization programs in developing countries. To overcome this problem, combination with diphtheria-tetanus-pertussis (DTP) vaccine or reduction in the dose of Hib vaccine has been proposed. To evaluate the immunogenicity and adverse reactions from lower doses of Hib-polyribosylphosphate (PRP) conjugated with tetanus toxoid (PRP-T), a double-blind study was conducted in Jakarta, Indonesia, and its suburbs. A total of 1048 infants 6 weeks to 6 months of age received three doses of DTP vaccine combined with the usual 10 microg dose or with a reduced dose of 5, 2.5 or 1.25 microg of PRP-T at two-monthly intervals. Antibodies were measured prior to the first dose and 4-6 weeks following the third dose. Adverse reactions were similar among all four groups. The only significant difference was a higher rate of irritability (p<0.02) and of temperature elevation >38 degrees C (p<0.009) after doses 1 and 2 in the lowest dose group (1.25 microg PRP-T) compared to the other groups. All participants tested had a 4-fold increase in antibodies against all DTP antigens. In addition, after a fourth booster dose of Hib, 99.6% of infants produced >or=0.15 microg/ml of antibody to Hib-PRP, and 96.4% showed levels >or=1.0 microg/ml after primary immunization, level that correlate with short- and long-term immunity, respectively. Antibody titers to the PRP antigen showed no significant differences among dosage groups with the exception of the 5.0 microg group, which had a significantly higher GMC than the 1.25 microg group (p<0.012). This study demonstrates that primary vaccination with half, one-fourth, or one-eighth of the usual dose of PRP-T, combined with DTP vaccine, produces protective immune responses, and has side effects that are comparable to DTP vaccination alone. In these lower dosages, PRP-T conjugate vaccine can lower vaccine costs to a level that is affordable for infant immunization programs in developing countries.
在工业化国家,b型流感嗜血杆菌(Hib)结合疫苗的广泛使用已导致侵袭性Hib疾病的发病率大幅下降,但该疫苗的成本使其无法纳入发展中国家的基础免疫计划。为克服这一问题,有人提议将其与白喉-破伤风-百日咳(DTP)疫苗联合使用或降低Hib疫苗的剂量。为评估低剂量Hib-多聚核糖磷酸(PRP)与破伤风类毒素(PRP-T)结合疫苗的免疫原性和不良反应,在印度尼西亚雅加达及其郊区进行了一项双盲研究。共有1048名6周龄至6月龄的婴儿每隔两个月接受三剂DTP疫苗,分别联合常规的10微克剂量或5微克、2.5微克或1.25微克的减量PRP-T。在第一剂之前和第三剂之后4至6周测量抗体。所有四组的不良反应相似。唯一显著的差异是,与其他组相比,最低剂量组(1.25微克PRP-T)在第1剂和第2剂后出现烦躁的比例更高(p<0.02),体温升高超过38摄氏度的比例更高(p<0.009)。所有受试参与者针对所有DTP抗原的抗体均增加了4倍。此外,在第四剂Hib加强免疫后,99.6%的婴儿产生了≥0.15微克/毫升的抗Hib-PRP抗体,96.4%的婴儿在初次免疫后抗体水平≥1.0微克/毫升,这两个水平分别与短期和长期免疫力相关。除5.0微克组的几何平均浓度(GMC)显著高于1.25微克组(p<0.012)外,各剂量组针对PRP抗原的抗体滴度无显著差异。这项研究表明,用常规剂量一半、四分之一或八分之一的PRP-T联合DTP疫苗进行初次接种可产生保护性免疫反应,且副作用与单独接种DTP疫苗相当。在这些较低剂量下,PRP-T结合疫苗可将疫苗成本降低到发展中国家婴儿免疫计划能够承受的水平。