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Meningococcal groups C and y and haemophilus b tetanus toxoid conjugate vaccine (HibMenCY-TT; MenHibrix?): A review

机译:脑膜炎双球菌C和y组和嗜血杆菌b破伤风类毒素结合疫苗(HibMenCY-TT; MenHibrix?):综述

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The meningococcal groups C and Y and Haemophilus b (Hib) tetanus toxoid conjugate vaccine (HibMenCY-TT) contains Neisseria meningitidis serogroup C and Y capsular polysaccharide antigens, and Hib capsular polysaccharide [polyribosyl-ribitol-phosphate (PRP)]. The HibMenCY-TT vaccine is available in the USA for use as active immunization to prevent invasive disease caused by N. meningitidis serogroups C (MenC) and Y (MenY), and Hib in children 6 weeks-18 months of age. HibMenCY-TT is the first meningococcal vaccine available for use in the USA that can be administered to infants as young as 6 weeks of age. In a randomized, controlled, phase III clinical trial, the HibMenCY-TT vaccine, administered to infants at 2, 4, 6 and 12-15 months of age, was immunogenic against MenC and MenY, and met the prespecified criteria for immunogenicity. Anti-PRP antibodies, which have been shown to correlate with protection against Hib invasive disease, were also induced in the infants who received the HibMenCY-TT vaccine, with induced levels of this antibody noninferior to those occurring in the control group of infants who received a Hib tetanus toxoid conjugate vaccine at 2, 4, and 6 months and a single dose of Hib conjugated to N. meningitidis outer membrane protein at 12-15 months. In several randomized, controlled clinical trials, HibMenCY-TT was coadministered with vaccines that are routinely administered to infants and toddlers in the USA. These vaccines included: diphtheria and tetanus toxoids and acellular pertussis adsorbed, hepatitis B (recombinant) and inactivated poliovirus vaccine combined; 7-valent Streptococcus pneumoniae polysaccharide conjugate vaccine; measles, mumps and rubella vaccine; and varicella vaccine. Coadministration of these vaccines did not interfere with the immunogenicity of the HibMenCY-TT vaccine. Similarly, immune responses to the coadministered vaccines were not affected by the HibMenCY-TT vaccine. The tolerability profile of the HibMenCY-TT vaccine in infants and toddlers in the phase III trial was considered to be clinically acceptable and comparable to that of the Hib conjugate vaccines received by the control group.
机译:脑膜炎球菌C和Y组和嗜血杆菌b(Hib)破伤风类毒素结合疫苗(HibMenCY-TT)包含脑膜炎奈瑟氏球菌血清C和Y荚膜多糖抗原,以及Hib荚膜多糖[聚核糖基核糖磷酸(PRP)]。 HibMenCY-TT疫苗在美国有售,可以用作主动免疫,以预防由脑膜炎双球菌血清群C(MenC)和Y(MenY)引起的侵袭性疾病,以及针对6周至18个月大的儿童的Hib。 HibMenCY-TT是美国首个可用于6周龄婴儿的脑膜炎球菌疫苗。在一项随机,对照的III期临床试验中,向2、4、6和12-15个月大的婴儿接种的HibMenCY-TT疫苗对MenC和MenY具有免疫原性,并符合预先设定的免疫原性标准。已经显示,与接种HibMenCY-TT疫苗的婴儿相关的抗PRP抗体也已被证明与针对Hib侵袭性疾病的保护作用相关,该抗体的诱导水平不亚于接受该疫苗的婴儿的对照组中的抗体水平。在第2、4和6个月时接种Hib破伤风类毒素结合疫苗,在第12-15个月时单剂结合至脑膜炎双球菌外膜蛋白的Hib。在一些随机,对照的临床试验中,HibMenCY-TT与美国常规向婴幼儿注射的疫苗合用。这些疫苗包括:吸附的白喉和破伤风类毒素和无细胞百日咳疫苗,乙型肝炎(重组)和灭活脊髓灰质炎病毒疫苗; 7价肺炎链球菌多糖结合疫苗;麻疹,腮腺炎和风疹疫苗;和水痘疫苗。这些疫苗的共同给药不会干扰HibMenCY-TT疫苗的免疫原性。同样,HibMenCY-TT疫苗不影响对共同接种疫苗的免疫反应。在III期试验中,HibMenCY-TT疫苗在婴幼儿中的耐受性被认为是临床可接受的,与对照组接受的Hib结合疫苗的耐受性相当。

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