Zerbini Cristiano A F, Ribeiro Dos Santos Rodrigo, Jose Nunes Maria, Soni Jyoti, Li Ping, Jain Varsha K, Ofori-Anyinam Opokua
Centro Paulista de Investigação Clinica, São Paulo, SP, Brazil.
Universidade Federal de Minas Gerais, Faculdade de Medicina, Santa Casa de Belo Horizonte, Belo Horizonte, MG, Brazil.
Braz J Infect Dis. 2017 Jan-Feb;21(1):63-70. doi: 10.1016/j.bjid.2016.10.003. Epub 2016 Nov 29.
The World Health Organization influenza forecast now includes an influenza B strain from each of the influenza B lineages (B/Yamagata and B/Victoria) for inclusion in seasonal influenza vaccines. Traditional trivalent influenza vaccines include an influenza B strain from one lineage, but because two influenza B lineages frequently co-circulate, the effectiveness of trivalent vaccines may be reduced in seasons of influenza B vaccine-mismatch. Thus, quadrivalent vaccines may potentially reduce the burden of influenza compared with trivalent vaccines. In this Phase III, open-label study, we assessed the immunogenicity and safety of Southern Hemisphere inactivated quadrivalent influenza vaccine (Fluarix™ Tetra) in Brazilian adults (NCT02369341). The primary objective was to assess hemagglutination-inhibition antibody responses against each vaccine strain 21 days after vaccination in adults (aged ≥18-60 years) and older adults (aged >60 years). Solicited adverse events for four days post-vaccination, and unsolicited adverse events and serious adverse events for 21 days post-vaccination were also assessed. A total of 63 adults and 57 older adults received one dose of inactivated quadrivalent influenza vaccine at the beginning of the 2015 Southern Hemisphere influenza season. After vaccination, in adults and older adults, the hemagglutination-inhibition titers fulfilled the European licensure criteria for immunogenicity. In adults, the seroprotection rates with HI titer ≥1:40 were 100% (A/H1N1), 98.4% (A/H3N2), 100% (B/Yamagata), and 100% (B/Victoria); in older adults were 94.7% (A/H1N1), 96.5% (A/H3N2), 100% (B/Yamagata), and 100% (B/Victoria). Pain was the most common solicited local adverse events in adults (27/62) and in older adults (13/57), and the most common solicited general adverse events in adults was myalgia (9/62), and in older adults were myalgia and arthralgia (both 2/57). Unsolicited adverse events were reported by 11/63 adults and 10/57 older adults. The study showed that inactivated quadrivalent influenza vaccine was immunogenic and well-tolerated in Brazilian adults and older adults.
世界卫生组织的流感预测现在纳入了来自乙型流感每个谱系(B/山形株和B/维多利亚株)的一种乙型流感毒株,用于季节性流感疫苗。传统的三价流感疫苗包含来自一个谱系的一种乙型流感毒株,但由于两种乙型流感谱系经常同时流行,在乙型流感疫苗不匹配的季节,三价疫苗的效力可能会降低。因此,与三价疫苗相比,四价疫苗可能会减轻流感负担。在这项III期开放标签研究中,我们评估了南半球灭活四价流感疫苗(Fluarix™ Tetra)在巴西成年人(NCT02369341)中的免疫原性和安全性。主要目标是评估18至60岁成年人及60岁以上老年人在接种疫苗21天后针对每种疫苗毒株的血凝抑制抗体反应。还评估了接种疫苗后4天内的预期不良事件,以及接种疫苗后21天内的非预期不良事件和严重不良事件。在2015年南半球流感季节开始时,共有63名成年人和57名老年人接种了一剂灭活四价流感疫苗。接种疫苗后,在成年人和老年人中,血凝抑制效价均符合欧洲免疫原性许可标准。在成年人中,血凝抑制效价≥1:40的血清保护率分别为:甲型H1N1流感100%、甲型H3N2流感98.4%、乙型山形株流感100%、乙型维多利亚株流感100%;在老年人中分别为:甲型H1N1流感94.7%、甲型H3N2流感96.5%、乙型山形株流感100%、乙型维多利亚株流感100%。疼痛是成年人(27/62)和老年人(13/57)中最常见的预期局部不良事件,成年人中最常见的预期全身不良事件是肌痛(9/62),老年人中是肌痛和关节痛(均为2/57)。11/63名成年人和10/57名老年人报告了非预期不良事件。该研究表明,灭活四价流感疫苗在巴西成年人和老年人中具有免疫原性且耐受性良好。