Lin Tzou-Yien, Wang Ying-Hsiang, Huang Yhu-Chering, Chiu Cheng-Hsun, Lin Pen-Yi, Chen Chih-Jung, Chavand Pascale, Ortiz Esteban
Department of Pediatrics, Chang Gung Children's Hospital, Chang Gung Memorial Hospital, Chang Gung University Medicine, Taoyuan, Taipei, Taiwan.
Int J Infect Dis. 2007 Nov;11(6):488-95. doi: 10.1016/j.ijid.2007.01.006. Epub 2007 Mar 8.
To evaluate antibody persistence one year after three-dose primary vaccination and booster immune response during the second year of life for a fully liquid diphtheria-tetanus-acellular pertussis-inactivated poliomyelitis-Haemophilus influenzae type b (DTaP-IPV-PRP approximately T) vaccine.
Infants at 18-19 months of age were given a booster dose of either DTaP-IPV-PRP approximately T (group A) or DTaP-IPV plus PRP approximately T at separate injection sites (group B), after primary vaccination at two, four and six months of age, with the same vaccines. Antibody concentrations were measured pre- and post-booster. Reactogenicity and safety were evaluated from parent reports.
Before the booster dose, 93.1% of group A and 95.1% of group B children still had anti-PRP antibody titers > or =0.15 microg/ml. All children had antibody levels believed to protect against tetanus, polio 1 (except one subject in group B), polio 2, polio 3, and diphtheria (except one subject in group A). At least 94% of children still had antibody concentrations > or =5 ELISA units (EU) to pertussis antigens (pertussis toxoid (PT), filamentous hemagglutinin (FHA), pertactin (PRN), fimbriae 2 and 3 (FIM2+3)). One month after the booster dose, all subjects achieved antibody concentrations or titers believed to be protective for PRP (polyribose ribitol phosphate)(> or =1 microg/ml), diphtheria and tetanus (> or =0.1 IU/ml) and poliovirus types 1, 2, and 3 (> or =81/dil.), and at least 90.5% of subjects had four-fold increases in antibody concentrations to pertussis antigens following the booster. Anti-PRP geometric mean titers (GMTs) increased from 1.07 to 59.6 microg/ml and from 1.8 to 62.2 microg/ml in groups A and B, respectively. Both vaccine groups showed low reactogenicity rates.
The fully liquid pentavalent DTaP-IPV-PRP approximately T vaccine is highly immunogenic, with good antibody persistence for each antigen approximately one year after primary vaccination and strong booster responses at 18-19 months of age. Because this combined vaccine is fully liquid, requiring no reconstitution of lyophilized PRP approximately T, the ease of use and proper administration are improved.
评估全液体剂型白喉-破伤风-无细胞百日咳-灭活脊髓灰质炎- b型流感嗜血杆菌(DTaP-IPV-PRP大约T)疫苗在三剂基础免疫接种一年后抗体的持久性以及生命第二年的加强免疫反应。
18至19月龄的婴儿在2、4和6月龄用相同疫苗进行基础免疫后,分别在不同注射部位接种一剂DTaP-IPV-PRP大约T(A组)或DTaP-IPV加PRP大约T(B组)进行加强免疫。在加强免疫前后测量抗体浓度。根据家长报告评估反应原性和安全性。
在加强免疫前,A组93.1%的儿童和B组95.1%的儿童抗PRP抗体滴度仍≥0.15μg/ml。所有儿童的抗体水平被认为可预防破伤风、脊髓灰质炎1型(B组有1名受试者除外)、脊髓灰质炎2型、脊髓灰质炎3型和白喉(A组有1名受试者除外)。至少94%的儿童针对百日咳抗原(百日咳毒素(PT)、丝状血凝素(FHA)、百日咳杆菌黏附素(PRN)、菌毛2和3(FIM2 + 3))的抗体浓度仍≥5酶联免疫吸附测定单位(EU)。加强免疫后1个月,所有受试者的PRP(多核糖醇磷酸)(≥1μg/ml)、白喉和破伤风(≥0.1 IU/ml)以及脊髓灰质炎病毒1、2和3型(≥81/稀释度)的抗体浓度或滴度达到被认为具有保护作用的水平,并且至少90.5%的受试者在加强免疫后针对百日咳抗原的抗体浓度增加了四倍。A组和B组的抗PRP几何平均滴度(GMT)分别从1.07μg/ml增至59.6μg/ml和从1.8μg/ml增至62.2μg/ml。两个疫苗组均显示出较低的反应原性发生率。
全液体剂型五价DTaP-IPV-PRP大约T疫苗具有高度免疫原性,基础免疫接种后每种抗原的抗体持久性良好,在18至19月龄时加强免疫反应强烈。由于这种联合疫苗是全液体剂型,无需复溶冻干的PRP大约T,因此使用便利性和接种的正确性均得到改善。