首页> 外文期刊>Human vaccines >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 A randomized, controlled trial in children primed according to a 2 + 1 schedule in infancy
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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 A randomized, controlled trial in children primed according to a 2 + 1 schedule in infancy

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-水痘疫苗联合接种的学龄前儿童加强免疫接种根据2 + 1时间表对儿童进行的随机对照试验婴儿期

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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 (NCT00871000), the immunogenicity, safety and reactogenicity of a booster dose of reduced-antigen content diphtheria-tetanus-acellular pertussis-inactivated poliovirus vaccine (dTpa-IPV; GSK Biologicals Soostrix-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 Illb, 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: Three-hundred and five 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,百日咳发生在年龄较大的儿童,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。在这项研究(NCT00871000)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-方法:对意大利学龄前儿童进行IPV; GSK Biologicals Soostrix-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:5岁健康儿童在这一阶段的IIlbb加强研究中,在常规疫苗接种中接种了三剂基于DTPa的疫苗接种了-6年并随机分配(1:1),以接受单剂dTpa-IPV或DTPa-IPV; 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。结果:入选了350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具有血清保护/血清阳性。 99.3%的dTpa-IPV和60.4%的DTPa-IPV受试者抗PRN呈血清反应阳性;加强后98-100%的受试者对MMRV抗原呈血清阳性。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。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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