Castillo de Febres O, Decker M D, Estopinan M, Bordones G, Edwards K M
Department of Pediatrics, University of Carabobo, Valencia, Venezuela.
Pediatr Infect Dis J. 1994 Jul;13(7):635-9. doi: 10.1097/00006454-199407000-00010.
The safety and immunogenicity of primary immunization at 2, 4 and 6 months of age with Haemophilus influenzae type b capsular polysaccharide conjugated to tetanus toxoid (PRP-T; Act-HIB) were evaluated in infants in Valencia, Venezuela. In order better to assess reactions to PRP-T, subjects received their initial PRP-T vaccine a mean of 6.5 days after their initial diphtheria-tetanus-pertussis (DTP) vaccine. The PRP-T vaccine was well tolerated. Serum was obtained at ages 2 and 7 months (before the first and 1 month after the third PRP-T dose). Antibody responses were compared with those from Nashville infants who had received PRP-T and DTP simultaneously in a previous trial. The preimmunization titers in the Venezuelan and Nashville infants did not differ. The geometric mean postimmunization titer in the Venezuelan infants was 37.9 micrograms/ml, as compared with 3.63 micrograms/ml in the Nashville infants (P < 0.00001). Possible explanations for the exceptional antibody response of these Venezuelan infants to PRP-T include carrier priming caused by prior DTP immunization, synergy associated with the specific DTP vaccine used, preimmunization immunologic experience that differed from their United States counterparts and genetic differences that altered response to the vaccines. Further studies are proposed to evaluate these possibilities.
在委内瑞拉巴伦西亚的婴儿中,评估了2、4和6月龄时用与破伤风类毒素结合的b型流感嗜血杆菌荚膜多糖(PRP-T;Act-HIB)进行初次免疫的安全性和免疫原性。为了更好地评估对PRP-T的反应,受试者在初次接种白喉-破伤风-百日咳(DTP)疫苗后平均6.5天接受了初次PRP-T疫苗。PRP-T疫苗耐受性良好。在2个月和7个月龄时(第一次PRP-T剂量之前和第三次PRP-T剂量后1个月)采集血清。将抗体反应与之前一项试验中同时接受PRP-T和DTP的纳什维尔婴儿的反应进行比较。委内瑞拉婴儿和纳什维尔婴儿的免疫前滴度没有差异。委内瑞拉婴儿免疫后的几何平均滴度为37.9微克/毫升,而纳什维尔婴儿为3.63微克/毫升(P<0.00001)。这些委内瑞拉婴儿对PRP-T产生异常抗体反应的可能解释包括先前DTP免疫引起的载体启动、与所用特定DTP疫苗相关的协同作用、与美国同龄人不同的免疫前免疫经验以及改变对疫苗反应的基因差异。建议进行进一步研究以评估这些可能性。