Black Steven, Friedland Leonard R, Ensor Kathleen, Weston Wayde M, Howe Barbara, Klein Nicola P
Stanford University, Palo Alto, CA, USA.
Pediatr Infect Dis J. 2008 Apr;27(4):341-6. doi: 10.1097/INF.0b013e3181616180.
In the United States, diphtheria-tetanus-acellular pertussis (DTaP) and inactivated poliovirus (IPV) booster vaccinations are recommended for children 4-6 years of age. A combined DTaP-IPV vaccine is being developed, which would reduce by one the number of injections in this age group.
Children 4-6 years of age were randomized (1:1:1:1) to receive booster vaccination with 1 of 3 combined DTaP-IPV lots plus the measles, mumps, and rubella vaccine (N = 3156 for pooled lots) or separate doses of DTaP + IPV + measles, mumps, and rubella vaccine (N = 1053). Immunogenicity was assessed in a subset of children (N = 1331). Safety (solicited and unsolicited symptoms) including detailed assessment of local swelling reactions, was assessed in all children.
Increases in antibody geometric mean concentrations/titers 1 month after vaccination were observed for the diphtheria, tetanus, acellular pertussis, and polio antigens. At least 92.2% of combined DTaP-IPV subjects and 92.6% of separate DTaP + IPV subjects had a postvaccination booster response for one or more DTaP antigens. Booster responses to one or more poliovirus antigens were observed in at least 96.6% of combined DTaP-IPV subjects and 92.8% of separate DTaP + IPV subjects. The combined DTaP-IPV vaccine was noninferior to separately administered DTaP and IPV vaccines with respect to DTaP antigen booster response rates and poliovirus antibody geometric mean titers ratios. Reporting of solicited local and systemic events was comparable between both groups.
The combination DTaP-IPV vaccine provided immunogenicity and reactogenicity that is comparable to separately administered DTaP and IPV vaccines, with the advantage of requiring one less injection.
在美国,建议4至6岁的儿童接种白喉-破伤风-无细胞百日咳(DTaP)和灭活脊髓灰质炎病毒(IPV)加强疫苗。一种联合DTaP-IPV疫苗正在研发中,这将减少该年龄组的注射次数。
将4至6岁的儿童随机分为四组(1:1:1:1),分别接受三种联合DTaP-IPV批次中的一种加麻疹、腮腺炎和风疹疫苗的加强接种(合并批次N = 3156),或分别接种DTaP + IPV +麻疹、腮腺炎和风疹疫苗(N = 1053)。在一部分儿童(N = 1331)中评估免疫原性。在所有儿童中评估安全性(主动和被动报告的症状),包括对局部肿胀反应的详细评估。
接种疫苗1个月后,观察到白喉、破伤风、无细胞百日咳和脊髓灰质炎抗原的抗体几何平均浓度/滴度有所增加。至少92.2%的联合DTaP-IPV受试者和92.6%的单独接种DTaP + IPV受试者对一种或多种DTaP抗原产生了接种后加强反应。在至少96.6%的联合DTaP-IPV受试者和92.8%的单独接种DTaP + IPV受试者中观察到对一种或多种脊髓灰质炎病毒抗原的加强反应。联合DTaP-IPV疫苗在DTaP抗原加强反应率和脊髓灰质炎病毒抗体几何平均滴度比值方面不劣于单独接种的DTaP和IPV疫苗。两组主动报告的局部和全身事件情况相当。
联合DTaP-IPV疫苗提供的免疫原性和反应原性与单独接种的DTaP和IPV疫苗相当,且具有少注射一针的优势。