Prevention of rare diseases: how revolutionary techniques can help vulnerable individuals-the example of serogroup B meningococcal infection.

E David McIntosh, Victor Carey, Daniela Toneatto, Peter Dull, James Wassil
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引用次数: 15

Abstract

In countries with established programmes for vaccination of infants, toddlers and adolescents with meningococcal conjugate vaccines, serogroup B invasive meningococcal disease remains the major cause of septicaemia and meningitis in the paediatric and adolescent age groups. Novartis has developed a serogroup B meningococcal vaccine, 4CMenB, to meet this need. We reviewed all 4CMenB studies. The studies found 4CMenB to be highly immunogenic when administered in all schedules, with protective antibody levels (serum bactericidal antibody titres ≥4 or ≥5 with human complement, hSBA) against serogroup B strains expressing vaccine antigens in >95% of vaccinated cohorts. When antibody levels waned, all tested groups demonstrated booster responses. Although possibly an underestimation, the Meningococcal Antigen Typing System (MATS) technique predicts that global coverage of 4CMenB against all serogroup B strains is in the range 66% (Canada) to 91% (USA). The vaccine was found to be generally well tolerated, although local and systemic reactions, notably fever in infants, typical of many vaccines, were increased following concomitant administration of 4CMenB with routine vaccines. When tested, prophylactic paracetamol significantly decreased the frequency and severity of reactions in infants, with no clinically significant impact on immunogenicity of 4CMenB or concomitant routine vaccines. The vaccine is approved for use in the following age groups in the European Union (2 months+), Canada (2 months through 17 years), Australia (2 months+) and Chile (2 months+), following clinical evaluation in 4843 infants and toddlers, and 1712 adolescents and adults, in schedules including a three-dose (2, 3, 4 or 2, 4, 6 months) and a two-dose (6-11 months) infant series with a booster in the second year of life, a two-dose series in toddlers (12-23 months) and children (2-10 years) given 2 months apart (with a booster at least in the EU), and a two-dose series in adolescents (11-17 years) given 1-6 months apart. 4CMenB presents a solution to the unmet medical need of offering protection against serogroup B invasive meningococcal disease in all age groups above 2 months.

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罕见疾病的预防:革命性技术如何帮助易受伤害的个体——以血清B群脑膜炎球菌感染为例。
在制订了为婴儿、幼儿和青少年接种脑膜炎球菌结合疫苗方案的国家,血清B群侵袭性脑膜炎球菌病仍然是造成儿童和青少年败血症和脑膜炎的主要原因。为了满足这一需求,诺华公司开发了一种血清B群脑膜炎球菌疫苗4CMenB。我们回顾了所有4CMenB研究。研究发现,在所有接种计划中,4CMenB具有高度的免疫原性,在>95%的接种队列中,对表达疫苗抗原的血清B组菌株具有保护性抗体水平(人补体血清杀菌抗体滴度≥4或≥5)。当抗体水平下降时,所有测试组都表现出增强反应。尽管可能存在低估,但脑膜炎球菌抗原分型系统(MATS)技术预测,4CMenB对所有血清B组菌株的全球覆盖率在66%(加拿大)至91%(美国)之间。研究发现,该疫苗总体耐受性良好,但在常规疫苗同时使用4CMenB疫苗后,局部和全身反应,特别是婴儿发烧(许多疫苗的典型症状)增加。经测试,预防性扑热息痛可显著降低婴儿反应的频率和严重程度,对4CMenB或伴随常规疫苗的免疫原性无临床显著影响。在对4843名婴儿和幼儿以及1712名青少年和成人进行临床评估后,该疫苗被批准在以下年龄组中使用:欧盟(2个月以上)、加拿大(2个月至17岁)、澳大利亚(2个月以上)和智利(2个月以上),时间表包括三剂(2、3、4或2、4、6个月)和两剂(6-11个月)婴儿系列,并在生命的第二年加强接种。幼儿(12-23个月)和儿童(2-10岁)的两剂系列疫苗间隔2个月接种(至少在欧盟有加强剂),青少年(11-17岁)的两剂系列疫苗间隔1-6个月接种。4CMenB提供了一种解决方案,以满足在2个月以上的所有年龄组提供针对血清B群侵袭性脑膜炎球菌病的保护的未满足的医疗需求。
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