首页> 美国卫生研究院文献>Human Vaccines Immunotherapeutics >Booster vaccination of pre-school children with reduced-antigen-content diphtheria-tetanus-acellular pertussis-inactivated poliovirus vaccine co-administered with measles-mumps-rubella-varicella vaccine
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Booster vaccination of pre-school children with reduced-antigen-content diphtheria-tetanus-acellular pertussis-inactivated poliovirus vaccine co-administered with measles-mumps-rubella-varicella vaccine

机译:降低抗原含量的白喉-破伤风-无细胞百日咳灭活的脊髓灰质炎病毒疫苗与麻疹-腮腺炎-风疹-水痘疫苗联合应用对学龄前儿童的加强疫苗接种

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摘要

>Background: Pertussis occurs in older children, adolescents and adults due to waning immunity after primary vaccination. Booster vaccination for pre-school children has been recommended in Italy since 1999. In this study (), the immunogenicity, safety and reactogenicity of a booster dose of reduced-antigen content diphtheria-tetanus-acellular pertussis-inactivated poliovirus vaccine (dTpa-IPV; GSK Biologicals Boostrix™-Polio; 3-component pertussis) vs. full-strength DTPa-IPV vaccine (sanofi-pasteur—MSD Tetravac™; 2-component pertussis) was evaluated in pre-school Italian children.  >Methods: Healthy children aged 5–6 y primed in a routine vaccination setting with three doses of DTPa-based vaccines were enrolled and randomized (1:1) in this phase IIIb, booster study to receive a single dose of dTpa-IPV or DTPa-IPV; the MMRV vaccine was co-administered. Antibody concentrations/titers against diphtheria, tetanus, pertussis and poliovirus 1–3 were measured before and one month post-booster. Reactogenicity and safety was assessed.>Results: 305 subjects were enrolled of whom 303 (dTpa-IPV = 151; DTPa-IPV = 152) received booster vaccination. One month post-booster, all subjects were seroprotected/seropositive for anti-diphtheria, anti-tetanus, anti-PT, anti-FHA and anti-poliovirus 1–3; 99.3% of dTpa-IPV and 60.4% of DTPa-IPV subjects were seropositive for anti-PRN; 98–100% of subjects were seropositive against MMRV antigens post-booster. Pain at the injection site (dTpa-IPV: 63.6%; DTPa-IPV: 63.2%) and fatigue (dTpa-IPV: 26.5%; DTPa-IPV: 23.7%) were the most commonly reported solicited local and general symptoms, during the 4-d follow-up period. No SAEs or fatalities were reported.>Conclusions: The reduced-antigen-content dTpa-IPV vaccine was non-inferior to full-strength DTPa-IPV vaccine with respect to immunogenicity. The vaccine was well-tolerated and can be confidently used as a booster dose in pre-school children.
机译:>背景:由于初次接种疫苗后免疫力下降,百日咳常发生于年龄较大的儿童,青少年和成年人中。自1999年以来,意大利一直建议对学龄前儿童进行加强疫苗接种。在本研究中(),加强剂量的降低抗原含量的白喉-破伤风-无细胞百日咳灭活脊髓灰质炎病毒疫苗(dTpa-IPV)的免疫原性,安全性和反应原性;在意大利学龄前儿童中评估了GSK Biologics Boostrix™-Polio; 3组分百日咳)与全强度DTPa-IPV疫苗(sanofi-pasteur-MSD Tetravac™; 2组分百日咳)的比较。 >方法:在此IIIb期中,接受了常规疫苗接种和三剂DTPa疫苗接种的5-6岁健康儿童并随机分配(1:1),以加强研究以接受单次dTpa-IPV或DTPa-IPV的剂量; MMRV疫苗是共同使用的。在加强接种前和加强接种后一个月测量了针对白喉,破伤风,百日咳和脊髓灰质炎病毒1-3的抗体浓度/滴度。评估了反应原性和安全性。>结果:招募了305名受试者,其中303名(dTpa-IPV = 151; DTPa-IPV = 152)接受了加强免疫。加强免疫后一个月,所有受试者的抗白喉,抗破伤风,抗PT,抗FHA和抗脊髓灰质炎病毒1-3均为血清保护/血清阳性。 dTpa-IPV患者中99.3%和DTPa-IPV患者中60.4%抗PRN血清反应阳性;加强后98-100%的受试者血清抗MMRV抗原呈阳性。注射部位的疼痛(dTpa-IPV:63.6%; DTPa-IPV:63.2%)和疲劳(dTpa-IPV:26.5%; DTPa-IPV:23.7%)是在治疗期间最常引起的局部和一般症状。 4天随访期。未报告SAE或死亡。>结论:降低抗原含量的dTpa-IPV疫苗在免疫原性方面不逊于全强度DTPa-IPV疫苗。该疫苗耐受性良好,可以放心地用作学龄前儿童的加强剂量。

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