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Prevention of meningococcal infections in the first 2 years of life

机译:在生命的最初2年中预防脑膜炎球菌感染

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The spectrum of disease caused by Neisseria meningitidis includes bacteremia, fulminant sepsis (meningococcemia), meningitis, and pneumonia. The incidence of meningococcal infection has long been higher in infancy than adolescents or adults older than 65 years (a third group with an increased risk based on age). Five meningococcal serogroups (A, B, C, Y, and W135) cause the great majority of human disease. Sero-group B strains cause about two-thirds of disease in children younger than 6 years. For this reason, new meningococcal vaccine formulations have been developed and evaluated in children younger than 2 years. Of four meningococcal vaccines currently licensed in the United States, two conjugate products, (MenACWY-D [Menactra], Sanofi Pasteur; HibMenCY-TT [MenHibrix], GlaxoSmithKline), are recommended for infants and toddlers younger than 2 years who have an increased risk for invasive meningococcal disease. High-risk conditions are complement deficiencies, community outbreaks, functional or anatomic asplenia, and travel to high-risk areas in which serogroup A infection is prevalent. Recommendations vary by age, dosing, and indication between these two products. Both licensed products are immunogenic and have side-effect profiles that are considered safe for use. In most cases, concomitant use with other recommended childhood vaccines does not interfere with responses to these vaccines. As of yet, there has not been universal adoption of this immunization in the infant population by parents or providers. Factors that weigh against the implementation of a national routine infant program include the prevention of only 40 to 50 meningococcal cases, two to four deaths per year, and a relatively low case fatality among infants. Some argue that costs should not be considered a barrier because infant deaths and morbidity would be prevented. The availability of a serogroup B vaccine would improve impact and cost-effectiveness of a routine infant meningococcal vaccine program. Debate over the implementation of routine infant meningococcal vaccination in the United States is ongoing. This review focuses on vaccines for the prevention of N. meningitidis infection in infants and young toddlers in the first 2 years of life.
机译:由脑膜炎奈瑟氏球菌引起的疾病范围包括菌血症,暴发性败血症(脑膜炎球菌血症),脑膜炎和肺炎。长期以来,婴儿期脑膜炎球菌感染的发生率一直高于青少年或65岁以上的成年人(第三组患病风险随年龄增加)。五个脑膜炎球菌血清群(A,B,C,Y和W135)引起绝大多数人类疾病。 B群血清毒株在6岁以下的儿童中引起约三分之二的疾病。因此,已经开发出了新的脑膜炎球菌疫苗制剂,并在2岁以下的儿童中进行了评估。在美国目前许可的四种脑膜炎球菌疫苗中,建议对年龄在2岁以下的婴幼儿增加使用的两种结合产品(MenACWY-D [Menactra],赛诺菲巴斯德; HibMenCY-TT [MenHibrix],葛兰素史克)侵袭性脑膜炎球菌病的风险。高危情况包括补体缺乏症,社区暴发,功能或解剖无力,以及前往A血清群感染流行的高风险地区。在这两种产品之间,建议随年龄,剂量和适应症的不同而不同。两种许可产品均具有免疫原性,并具有被认为可以安全使用的副作用。在大多数情况下,与其他推荐的儿童期疫苗同时使用不会干扰对这些疫苗的反应。迄今为止,父母或提供者尚未在婴儿人群中普遍采用这种免疫方法。妨碍实施国家例行婴儿计划的因素包括仅预防40至50例脑膜炎球菌病例,每年2至4例死亡以及婴儿中较低的病死率。一些人认为,不应将成本视为障碍,因为这样可以避免婴儿的死亡和发病。 B血清群疫苗的可用性将改善常规婴儿脑膜炎球菌疫苗计划的影响和成本效益。关于在美国实施常规婴儿脑膜炎球菌疫苗的辩论仍在进行中。这篇综述的重点是预防出生后头2年婴儿和幼儿的脑膜炎奈瑟菌感染的疫苗。

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  • 来源
    《Pediatric annals.》 |2013年第8期|共8页
  • 作者

    WoodsC.R.;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 儿科学;
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  • 入库时间 2022-08-18 15:39:13

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