成人接种MenB-4C疫苗对抗遗传多样性血清B群脑膜炎球菌的血清杀菌抗体反应

Q2 Biochemistry, Genetics and Molecular Biology
Clinical and Vaccine Immunology Pub Date : 2017-01-05 Print Date: 2017-01-01 DOI:10.1128/CVI.00430-16
Serena Giuntini, Eduardo Lujan, Malick M Gibani, Christina Dold, Christine S Rollier, Andrew J Pollard, Dan M Granoff
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引用次数: 0

摘要

MenB-4C是一种预防血清B群疾病的脑膜炎球菌疫苗。该疫苗含有因子H结合蛋白(FHbp)和其他三种抗原,可引发血清杀菌抗体(SBA)。对于疫苗许可,从SBA对三种抗原特异性指示菌株的反应推断出有效性。这些结果与防止遗传多样性菌株传播的广泛保护之间的关系尚不清楚。20名成年人接种了两剂MenB-4C疫苗,接种间隔1至2个月。测定SBA对3株参考菌株和15株血清B组试验菌株(6株来自高校疫情)的活性。与免疫前滴度相比,70%、95%和95%的受试者对参考菌株的抗pora P1.4、抗nada和抗fhbp抗体滴度分别升高≥4倍。相比之下,只有25%至45%的受试者对15种测试菌株中的10种(包括8种表达疫苗中一到三种抗原的菌株)的反应增加了4倍以上。在1个月时,大多数受试者与
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Serum Bactericidal Antibody Responses of Adults Immunized with the MenB-4C Vaccine against Genetically Diverse Serogroup B Meningococci.

MenB-4C is a meningococcal vaccine for the prevention of serogroup B disease. The vaccine contains factor H binding protein (FHbp) and three other antigens that can elicit serum bactericidal antibodies (SBA). For vaccine licensure, efficacy was inferred from the SBA responses against three antigen-specific indicator strains. The relation between those results and broad protection against circulating genetically diverse strains is not known. Twenty adults were immunized with two doses of MenB-4C given 1 to 2 months apart. SBA activity against 3 reference strains and 15 serogroup B test strains (6 from college outbreaks) was measured. Compared to the preimmunization titers, 70%, 95%, and 95% of subjects had ≥4-fold increases in the titers of anti-PorA P1.4, anti-NadA, and anti-FHbp antibodies against the reference strains, respectively. In contrast, only 25 to 45% of the subjects had ≥4-fold increases in responses to 10 of the 15 test strains, including 8 that expressed one to three of the antigens in the vaccine. At 1 month, the majority of subjects with <4-fold titer increases had serum titers of ≥1:4, which are considered sufficient for protection. However, the titers against four strains declined to <1:4 by 4 to 6 months in one-third to greater than 50% of the subjects tested. Clinically relevant isolates are often more resistant to SBA than the indicator strains used to measure antigen-specific SBA. A working model is that the percentage of subjects with titers of ≥1:4 at 1 month postimmunization correlates with short-term protection against that strain, whereas the percentage of subjects with ≥4-fold titer increases represents a more robust response. (The protocol used at the Oxford Vaccine Group has been registered at ClinicalTrials.gov under registration no. NCT02398396.).

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来源期刊
Clinical and Vaccine Immunology
Clinical and Vaccine Immunology 医学-传染病学
CiteScore
2.88
自引率
0.00%
发文量
0
审稿时长
1.5 months
期刊介绍: Cessation. First launched as Clinical and Diagnostic Laboratory Immunology (CDLI) in 1994, CVI published articles that enhanced the understanding of the immune response in health and disease and after vaccination by showcasing discoveries in clinical, laboratory, and vaccine immunology. CVI was committed to advancing all aspects of vaccine research and immunization, including discovery of new vaccine antigens and vaccine design, development and evaluation of vaccines in animal models and in humans, characterization of immune responses and mechanisms of vaccine action, controlled challenge studies to assess vaccine efficacy, study of vaccine vectors, adjuvants, and immunomodulators, immune correlates of protection, and clinical trials.
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