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用于幼儿的肺炎球菌结合疫苗。

Pneumococcal conjugate vaccine for young children.

作者信息

Selman S, Hayes D, Perin L A, Hayes W S

机构信息

School of Medicine and Biomedical Sciences, State University of New York at Buffalo, USA.

出版信息

Manag Care. 2000 Sep;9(9):49-52, 54, 56-7 passim.

PMID:11116663
Abstract

UNLABELLED

Pneumococcal disease is a common cause of morbidity and mortality in the pediatric population. Pneumococcal infections, which account for most serious bacterial disease in infancy and early childhood, are a major cause of acute otitis media, sinusitis, pneumonia, bacterial meningitis, and bacteremia. Streptococcus pneumoniae is the causative agent in a large percentage of these infections, although other microorganisms also play a role. The recent emergence of drug-resistant strains has provided a strong incentive for preventing pneumococcal infections by vaccination. However, the capsular polysaccharide pneumococcal vaccines used to immunize adults are neither immunogenic nor protective in young children due to poor antibody responses. Therefore, research has focused on development of additional immunogenic pneumococcal vaccines to provide long-term immunity in children < 2 years of age. The most promising approach has been the development of a protein-polysaccharide conjugate vaccine for the seven serotypes (4, 6B, 9V, 14, 18C, 19F, and 23F) that most commonly cause infections in childhood. An effective conjugate vaccine that protects against these serotypes has the potential to prevent 85 percent of bacteremia episodes, 83 percent of meningitis episodes, and 65 percent of otitis media cases in the U.S. among children younger than 6 years. The Food and Drug Administration (FDA) recently approved the first protein-polysaccharide conjugate vaccine to prevent invasive pneumococcal diseases in infants and toddlers < 2 years of age. This conjugated vaccine against pneumococcus uses the same technology as the successful vaccine against Haemophilus influenzae type b. It consists of an immunogenic but inert protein coupled covalently to the polysaccharide coat of the selected strains of pneumococci. The conjugated antigen induces a more powerful, T-cell-based immune response in infants, which is developed by the time they are 2 months of age. Some important questions regarding this vaccine for children < 2 years of age: Is the vaccine safe? Is it immunogenic? Is it efficacious in preventing invasive pneumococcal disease and controlling otitis media?

FINDINGS

Results of three randomized double-blind trials designed to evaluate the safety and immunogenicity of this vaccine in healthy children < 2 years of age were reported within the last three years. The studies found that the vaccine is safe and highly immunogenic for all seven serotypes. The most recent study, involving over 37,000 young children, also evaluated the vaccine's efficacy, and reported that the vaccine is highly effective in preventing invasive disease and has had an impact on otitis media.

CONCLUSIONS

The heptavalent pneumococcal conjugate vaccine is safe and highly effective in preventing pneumococcal meningitis and bacteremic pneumonia in young children < 2 years of age; it is less effective in preventing otitis media. Based on the results of three well-designed studies demonstrating the vaccine's safety, immunogenicity, and efficacy, the vaccine is safe and effective for active immunization of children < 2 years of age against invasive disease caused by seven Streptococcus pneumoniae serotypes included in the vaccine. At this time, there is no clear medical consensus regarding its safety and efficacy for control of otitis media in children < 2 years of age. This application has not been evaluated by the FDA. The pneumococcal conjugate vaccine should be considered experimental, and has not been shown to be safe or efficacious for Streptococcus pneumoniae disease other than that caused by the serotypes included in the vaccine and for invasive infection, such as bacteremia or meningitis, caused by other microorganisms.

摘要

未标记

肺炎球菌疾病是儿童发病和死亡的常见原因。肺炎球菌感染占婴儿和幼儿期最严重细菌性疾病的大多数,是急性中耳炎、鼻窦炎、肺炎、细菌性脑膜炎和菌血症的主要病因。肺炎链球菌是这些感染中很大一部分的病原体,尽管其他微生物也起作用。耐药菌株的近期出现为通过接种疫苗预防肺炎球菌感染提供了强大动力。然而,用于成人免疫的荚膜多糖肺炎球菌疫苗由于抗体反应不佳,在幼儿中既无免疫原性也无保护作用。因此,研究集中于开发额外的免疫原性肺炎球菌疫苗,以在2岁以下儿童中提供长期免疫力。最有前景的方法是开发针对最常导致儿童期感染的7种血清型(4、6B、9V、14、18C、19F和23F)的蛋白 - 多糖结合疫苗。一种有效预防这些血清型感染的结合疫苗有潜力在美国6岁以下儿童中预防85%的菌血症发作、83%的脑膜炎发作和65%的中耳炎病例。美国食品药品监督管理局(FDA)最近批准了第一种用于预防2岁以下婴幼儿侵袭性肺炎球菌疾病的蛋白 - 多糖结合疫苗。这种抗肺炎球菌结合疫苗采用了与成功的抗b型流感嗜血杆菌疫苗相同的技术。它由一种免疫原性但无活性的蛋白与所选肺炎球菌菌株的多糖外壳共价结合组成。结合抗原在婴儿中诱导更强大的基于T细胞的免疫反应,这种反应在他们2个月大时就已形成。关于这种2岁以下儿童疫苗的一些重要问题:疫苗安全吗?有免疫原性吗?在预防侵袭性肺炎球菌疾病和控制中耳炎方面有效吗?

研究结果

在过去三年中报告了三项旨在评估这种疫苗在2岁以下健康儿童中的安全性和免疫原性的随机双盲试验结果。研究发现该疫苗对所有7种血清型均安全且具有高度免疫原性。最近一项涉及超过37000名幼儿的研究还评估了疫苗的疗效,并报告该疫苗在预防侵袭性疾病方面非常有效,且对中耳炎有影响。

结论

七价肺炎球菌结合疫苗在预防2岁以下幼儿的肺炎球菌脑膜炎和菌血症性肺炎方面安全且高效;在预防中耳炎方面效果较差。基于三项精心设计的研究结果证明了疫苗的安全性、免疫原性和有效性,该疫苗对于2岁以下儿童主动免疫预防由疫苗中包含的7种肺炎链球菌血清型引起的侵袭性疾病是安全有效的。目前,关于其在2岁以下儿童控制中耳炎方面的安全性和有效性尚无明确的医学共识。此应用尚未经FDA评估。肺炎球菌结合疫苗应被视为实验性的,并且尚未证明对疫苗中包含的血清型以外的肺炎链球菌疾病以及由其他微生物引起的侵袭性感染(如菌血症或脑膜炎)安全或有效。

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