蚊(RTS,S):一种预防恶性疟原虫疟疾的新疫苗。

Kyle J Wilby, Tim T Y Lau, Samuel E Gilchrist, Mary H H Ensom
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引用次数: 34

摘要

目的:总结和评价有关蚊子(Mosquirix, RTS,S)的文献,了解这种新型疟疾候选疫苗在治疗和经济上的争议。资料来源:系统检索文献,检索词为moquirix;RTS, S;疟疾;疫苗;MEDLINE(1948- 2011年11月)、EMBASE(1980- 2011年11月)、国际药物文摘(1970- 2011年11月)、谷歌和谷歌学术。研究选择和数据提取:回顾了描述疫苗开发、药理学、药代动力学、疗效和安全性的临床试验。在疗效方面,对报告获得疟疾的临床试验进行了审查。提取有关研究设计、人群、研究期间、基线特征、临床结果、结果和质量评估者的信息。资料综合:纳入5项随机对照试验和4项随访推广研究。在2期试验中,预防临床疾病首次发作的疫苗在婴儿中的有效率为33-65%,在儿童中的有效率为30-53%。在3期试验中,疫苗在5-17个月儿童中的有效性为56%。在一些研究中,RTS,S减少了临床疟疾发作的次数,并预防了严重疟疾。疫苗效力的随访期为6至45个月。RTS, s25 μg肌内注射3次,婴幼儿隔1个月给药。RTS,S似乎通常耐受性良好。已报告了少数脑膜炎病例和癫痫发作(在接种疫苗后7天内)。结论:RTS,S在1期、2期和3期试验中显示出有效性和安全性,并具有降低全球疟疾发病率和死亡率的潜力。主要挑战包括确定免疫持续时间、评估其成本效益、在特殊人群中的使用以及在流行地区的传播。在进一步研究之前,RTS,S有可能成为第一种有效的疟疾疫苗的基准。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Mosquirix (RTS,S): a novel vaccine for the prevention of Plasmodium falciparum malaria.

Objective: To summarize and evaluate the literature for Mosquirix (RTS,S) and provide insight into the therapeutic and economic controversies of this novel malaria vaccine candidate.

Data sources: A systematic literature search was performed using the terms Mosquirix; RTS,S; malaria; vaccine; and Plasmodium in MEDLINE (1948-November 2011), EMBASE (1980-November 2011), International Pharmaceutical Abstracts (1970-November 2011), Google, and Google Scholar.

Study selection and data extraction: Clinical trials describing vaccine development, pharmacology, pharmacokinetics, efficacy, and safety were reviewed. For efficacy, clinical trials were reviewed that reported acquisition of malarial disease. Information regarding study design, population, study period, baseline characteristics, clinical outcomes, results, and assessors of quality was extracted.

Data synthesis: Five randomized controlled trials and 4 follow-up extension studies were identified. In Phase 2 trials, vaccine efficacy rates were 33-65% in infants and 30-53% in children for preventing the first episode of clinical disease. In Phase 3 trials, vaccine efficacy was 56% in children aged 5-17 months. RTS,S reduced the number of clinical malaria episodes and prevented severe malaria in several studies. The follow-up period for vaccine efficacy ranged from 6 to 45 months. RTS,S 25 μg is administered intramuscularly as 3 injections given 1 month apart for infants and children. RTS,S appears to be generally well tolerated. A few cases of meningitis and seizures (within 7 days of vaccination) have been reported.

Conclusions: RTS,S has demonstrated efficacy and safety in Phase 1, 2, and 3 trials, and has the potential to decrease morbidity and mortality from malaria worldwide. Major challenges include determination of the duration of immunity, assessment of its cost-effectiveness, its use in special populations, and its dissemination in endemic regions. Pending further studies, RTS,S has the potential to become the benchmark as the first effective vaccine against malaria.

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