Galiza E P, Heath P T
Division of Child Health, St. George's University of London, London.
Minerva Med. 2007 Apr;98(2):131-43.
The pneumococcus is currently the most common cause of vaccine-preventable death in children aged less than 5 years, and in 2002 was responsible for 716,000 deaths worldwide. Treatment with antibiotics was the main approach to contain the pneumococcus, however, even with effective antibiotics, pneumococcal meningitis has a poor prognosis and with the emergence of drug resistant pneumococcal disease the need for prevention by vaccine was evident. The first born pneumococcal vaccines were polysaccharide vaccines that unfortunately did not protect young children. The most vulnerable age group of children, less than 2 years of age, were without any form of protection from the pneumococcus until the licensure of a conjugate vaccine. Conjugation of bacteria polysaccharides to carrier proteins has been a significant milestone in the work of vaccine development and has been previously used successfully in the production of the Haemophilus influenzae-print type b vaccine. The seven-valent pneumococcal conjugate vaccine was first licensed in the USA in 2000 and in the European Union this conjugate vaccine was licensed in February 2001. Currently, fourteen countries have included this vaccine in their immunization programmes. Vaccination policies are found to differ greatly across Europe due to differences in local epidemiological situation, and also due to economic considerations. However, many countries are reviewing their own policies based on available data on the burden of pneumococcal disease. This review aims to give an overview about the pneumococcus, the development of the pneumococcal conjugate vaccine, and its impact.
肺炎球菌是目前5岁以下儿童中可通过疫苗预防的死亡的最常见原因,2002年在全球造成了71.6万人死亡。使用抗生素治疗是控制肺炎球菌的主要方法,然而,即使使用有效的抗生素,肺炎球菌性脑膜炎的预后也很差,而且随着耐药肺炎球菌疾病的出现,通过疫苗进行预防的必要性显而易见。首批肺炎球菌疫苗是多糖疫苗,但遗憾的是对幼儿没有保护作用。在2岁以下这一年龄段最易感染的儿童群体,在结合疫苗获得许可之前,没有任何形式的针对肺炎球菌的保护。将细菌多糖与载体蛋白结合是疫苗研发工作中的一个重要里程碑,此前已成功用于生产b型流感嗜血杆菌疫苗。七价肺炎球菌结合疫苗于2000年在美国首次获得许可,2001年2月在欧盟获得许可。目前,有14个国家已将该疫苗纳入其免疫规划。由于当地流行病学情况不同以及经济方面因素,欧洲各国的疫苗接种政策差异很大。然而,许多国家正在根据关于肺炎球菌疾病负担的现有数据审查自身政策。本综述旨在概述肺炎球菌、肺炎球菌结合疫苗的研发及其影响。