Marcinak J F, Ward M, Frank A L, Boyer K M, Froeschle J E, Hosbach P H
Department of Pediatrics, University of Illinois, Chicago 60612.
Am J Dis Child. 1993 Mar;147(3):290-4. doi: 10.1001/archpedi.1993.02160270052017.
To compare the immunogenicity and reactogenicity of a two-component acellular pertussis vaccine (BIKEN) with whole-cell diphtheria and tetanus toxoids and pertussis vaccine (WC-DTP) when administered to children aged 15 to 20 months.
A randomized, double-blind study.
Children in this study were from 12 general pediatric practices (11 were private and one was university-affiliated) and one inner-city university pediatric clinic.
Two hundred forty-six children aged 15 to 20 months who had received a three-dose primary series of standard WC-DTP vaccine during infancy.
Children were randomly assigned to receive either WC-DTP or one of three lots of acellular diphtheria and tetanus toxoids and pertussis vaccine (DT-aP) in a 1:3 ratio at the 11 private practices and in a 1:1 ratio at the university-affiliated practice and inner-city university pediatric clinic.
The DT-aP vaccines contained 23.4 micrograms each of pertussis toxin and filamentous hemagglutinin per 0.5 mL and the same concentrations of diphtheria and tetanus toxoids as WC-DTP. Serum samples were obtained on the day of immunization and 4 to 6 weeks later. Adverse reactions at 6, 24, 48, and 72 hours were recorded by parents who were contacted by telephone at 24 and 72 hours and 14 days after immunization.
MEASUREMENTS/MAIN RESULTS: An indirect enzyme-linked immunosorbent assay method was used to determine IgG antibody response to pertussis toxin and filamentous hemagglutinin and IgG, IgA, and IgM to tetanus toxoids; a Chinese hamster ovary cell assay was used to measure functional antibodies to pertussis toxin; serum neutralization on VERO cells assayed diphtheria anti-toxin. Recipients of the DT-aP vaccine had fewer local reactions in the first 6 to 48 hours and fewer systemic reactions at 24 hours than did recipients of the WC-DTP vaccine. Acetaminophen was administered to 31% of DT-aP recipients compared with 63% of WC-DTP recipients. Infants given DT-aP had higher geometric mean antibody titer levels against pertussis antigens after vaccination.
The BIKEN DT-aP vaccine used in this study is less reactogenic and more immunogenic for selected pertussis antigens than the WC-DTP vaccine in children aged 15 to 20 months.
比较双组分无细胞百日咳疫苗(BIKEN)与全细胞白喉破伤风类毒素及百日咳疫苗(WC-DTP)在15至20月龄儿童中接种时的免疫原性和反应原性。
一项随机、双盲研究。
本研究中的儿童来自12家普通儿科诊所(11家为私立,1家为大学附属医院)和1家市中心大学儿科诊所。
246名15至20月龄的儿童,他们在婴儿期接受了三剂标准的WC-DTP疫苗基础免疫系列。
在11家私立诊所,儿童以1:3的比例随机分配接受WC-DTP或三种无细胞白喉破伤风类毒素及百日咳疫苗(DT-aP)批次中的一种;在大学附属医院和市中心大学儿科诊所,儿童以1:1的比例随机分配。
DT-aP疫苗每0.5 mL含23.4微克百日咳毒素和丝状血凝素,白喉和破伤风类毒素的浓度与WC-DTP相同。在免疫当天和4至6周后采集血清样本。在免疫后24小时和72小时以及14天通过电话联系家长,记录其在6、24、48和72小时出现的不良反应。
测量指标/主要结果:采用间接酶联免疫吸附测定法测定对百日咳毒素和丝状血凝素的IgG抗体反应以及对破伤风类毒素的IgG、IgA和IgM;采用中国仓鼠卵巢细胞试验测量对百日咳毒素的功能性抗体;在VERO细胞上进行血清中和试验检测白喉抗毒素。与WC-DTP疫苗接种者相比,DT-aP疫苗接种者在最初6至48小时的局部反应更少,在24小时的全身反应更少。31%的DT-aP疫苗接种者使用了对乙酰氨基酚,而WC-DTP疫苗接种者的这一比例为63%。接种DT-aP的婴儿在接种疫苗后针对百日咳抗原的几何平均抗体滴度水平更高。
本研究中使用的BIKEN DT-aP疫苗在15至20月龄儿童中,与WC-DTP疫苗相比,对选定的百日咳抗原反应原性更低,免疫原性更强。