Hospital Clínico Universitario de Santiago de Compostela, Spain, and Vaccine Research Unit, Instituto de Investigación Sanitaria de Santiago, Spain.
Pediatr Infect Dis J. 2012 Apr;31(4):392-9. doi: 10.1097/INF.0b013e31824b972b.
As multiple vaccines are administered concomitantly during routine pediatric immunizations, it is important to ascertain the potential interference of any new vaccine on the immune response to the concomitantly administered vaccines. Immune responses to meningococcal serogroup C-tetanus toxoid conjugate vaccine (MnCC-TT) and the diphtheria and tetanus antigens in routine pediatric vaccines (diphtheria, tetanus, acellular pertussis-hepatitis B virus-inactivated poliovirus/Haemophilus influenza type b [DTaP-HBV-IPV/Hib] and DTaP-IPV+Hib) when given concomitantly with the 13-valent pneumococcal conjugate vaccine (PCV13) were compared with responses when given with PCV7. In addition, the immunogenicity and safety of PCV13 were assessed.
Healthy infants were randomized to receive PCV13 or PCV7 (ages 2, 4, 6 and 15 months), concomitant with MnCC-TT (2, 4 and 15 months), DTaP-HBV-IPV/Hib (2, 4 and 6 months), and DTaP-IPV+Hib (15 months).
Immune responses to MnCC-TT and to the diphtheria and tetanus antigens administered with PCV13 were noninferior to the responses observed when the vaccines were administered with PCV7; ≥96.6 (postinfant) and ≥99.4% (posttoddler) subjects achieved prespecified immune response levels to each antigen in each group. After the infant series, ≥93.0% of subjects receiving PCV13 achieved pneumococcal anticapsular immunoglobulin G concentrations ≥0.35 µg/mL for all serotypes except serotype 3 (86.2%), increasing to 98.1-100% for most serotypes (serotype 3: 93.6%) after the toddler dose. Local and systemic reactions were similar between groups.
Immune responses to MnCC-TT, and other childhood vaccines (DTaP-HBV-IPV/Hib, DTaP-IPV+Hib) were noninferior when concomitantly administered with PCV13 compared with PCV7. PCV13 does not interfere with MnCC-TT. PCV13 is highly immunogenic with a favorable safety profile.
在常规儿童免疫接种中同时接种多种疫苗,因此确定任何新疫苗对同时接种疫苗的免疫反应是否存在潜在干扰非常重要。比较了在接种 13 价肺炎球菌结合疫苗(PCV13)时同时接种脑膜炎球菌 C 群结合物-破伤风类毒素结合疫苗(MnCC-TT)和常规儿童疫苗(白喉、破伤风、无细胞百日咳-乙型肝炎病毒-灭活脊髓灰质炎病毒/流感嗜血杆菌[DTaP-HBV-IPV/Hib]和 DTaP-IPV+Hib)中的白喉和破伤风抗原的免疫应答与单独接种 PCV7 时的免疫应答。此外,还评估了 PCV13 的免疫原性和安全性。
健康婴儿随机接受 PCV13 或 PCV7(2、4、6 和 15 月龄),同时接种 MnCC-TT(2、4 和 15 月龄)、DTaP-HBV-IPV/Hib(2、4 和 6 月龄)和 DTaP-IPV+Hib(15 月龄)。
在接种 PCV13 时,MnCC-TT 和白喉、破伤风抗原的免疫应答与接种 PCV7 时的免疫应答相当;≥96.6%(婴儿期)和≥99.4%(幼儿期)的受试者达到了每组每种抗原的预定免疫应答水平。在婴儿系列接种后,≥93.0%的接受 PCV13 治疗的受试者在所有血清型中均达到了针对荚膜免疫球蛋白 G 的浓度≥0.35μg/ml,除血清型 3(86.2%)外,大多数血清型(血清型 3:93.6%)在幼儿剂量后增加到 98.1-100%。组间局部和全身反应相似。
与接种 PCV7 相比,同时接种 PCV13 时,MnCC-TT 以及其他儿童疫苗(DTaP-HBV-IPV/Hib、DTaP-IPV+Hib)的免疫应答无差异。PCV13 不会干扰 MnCC-TT。PCV13 具有高度的免疫原性,且安全性良好。