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多组份脑膜炎球菌 B 型疫苗(4CMenB;Bexsero(®)):在初级和加强免疫接种中的使用评价。

Multicomponent meningococcal serogroup B vaccine (4CMenB; Bexsero(®)): a review of its use in primary and booster vaccination.

机构信息

Adis, 41 Centorian Drive, Private Bag 65901, Mairangi Bay, North Shore, 0754, Auckland, New Zealand.

出版信息

BioDrugs. 2013 Jun;27(3):263-74. doi: 10.1007/s40259-013-0029-2.

Abstract

Multicomponent meningococcal serogroup B vaccine (4CMenB; Bexsero(®)) is a unique vaccine containing four main immunogenic components: three recombinant proteins combined with outer membrane vesicles derived from meningococcal NZ98/254 strain. After three doses of 4CMenB (administered at 2, 3, and 4 months or 2, 4, and 6 months of age) in vaccine-naive infants, the majority of infants had seroprotective human complement serum bactericidal assay (hSBA) antibody titers against the meningococcal serogroup B test strains selected to be specific for the vaccine antigens in randomized, open-label or observer-blind, multicenter, phase IIb or III trials. In extensions to the phase III trial, two doses of 4CMenB administered between 12 and 15 months of age in vaccine-naive infants, and a single booster dose of 4CMenB administered at 12 months of age in vaccine-experienced infants, also elicited robust immunogenic responses. In a phase IIb/III trial, the majority of adolescents (aged 11-17 years) achieved seroprotective hSBA antibody titers against meningococcal serogroup B test strains after two doses of 4CMenB, and a third dose did not appear to add any extra protection. In adults who were potentially at an increased risk of occupational exposure to meningococcal isolates, seroprotection rates were high after one dose of 4CMenB and increased further after two or three doses in a small noncomparative, two-center, phase II trial. The reactogenicity of 4CMenB was generally acceptable in clinical trials. However, the vaccine was associated with more solicited systemic adverse events (particularly fever) in infants when coadministered with routine infant vaccines than when these vaccines were administered alone. In conclusion, 4CMenB effectively elicited immune responses against meningococcal serogroup B test strains selected to be specific for the vaccine antigens in infants, adolescents, and adults.

摘要

四价脑膜炎球菌结合疫苗(4CMenB;Bexsero(®))是一种独特的疫苗,包含四种主要免疫原性成分:三种重组蛋白与源自脑膜炎奈瑟菌 NZ98/254 株的外膜囊泡结合。在疫苗初免婴儿中接种三剂 4CMenB(在 2、3 和 4 个月龄或 2、4 和 6 个月龄时接种)后,大多数婴儿对选择用于疫苗抗原的脑膜炎奈瑟菌 B 群测试株具有血清杀菌抗体滴度(hSBA)的血清保护性,该试验在随机、开放标签或观察者盲、多中心、IIb 期或 III 期临床试验中。在 III 期试验的扩展中,在疫苗初免婴儿中于 12 至 15 个月龄时接种两剂 4CMenB,以及在疫苗有经验婴儿中于 12 个月龄时接种一剂 4CMenB 加强针,也引起了强烈的免疫应答。在 IIb/III 期试验中,大多数青少年(11-17 岁)在接种两剂 4CMenB 后达到对脑膜炎奈瑟菌 B 群测试株的血清保护性 hSBA 抗体滴度,而第三剂似乎没有提供额外的保护。在有职业性接触脑膜炎奈瑟菌分离株风险增加的成年人中,在接种一剂 4CMenB 后,保护率很高,在小型非对照、双中心、II 期试验中接种两剂或三剂后进一步提高。4CMenB 的一般反应原性在临床试验中是可以接受的。然而,与单独接种这些疫苗相比,当与常规婴儿疫苗联合接种时,疫苗在婴儿中引起更多的疫苗相关全身不良事件(尤其是发热)。总之,4CMenB 在婴儿、青少年和成年人中有效诱导针对选择用于疫苗抗原的脑膜炎奈瑟菌 B 群测试株的免疫应答。

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