首页> 外文期刊>The annals of pharmacotherapy >Mosquirix (RTS,S): A novel vaccine for the prevention of Plasmodium falciparum malaria [Mosquirix (RTS,S): Un nouveau vaccine pour la prévention de la malaria à Plasmodium falciparum]
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Mosquirix (RTS,S): A novel vaccine for the prevention of Plasmodium falciparum malaria [Mosquirix (RTS,S): Un nouveau vaccine pour la prévention de la malaria à Plasmodium falciparum]

机译:Mosquirix(RTS,S):一种预防恶性疟原虫疟疾的新型疫苗[Mosquirix(RTS,S):一种预防恶性疟原虫疟疾的新型疫苗]

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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.
机译:目的:总结和评估有关蚊子的文献(RTS,S),并提供对该新型疟疾疫苗候选者在治疗和经济方面争议的见解。资料来源:使用术语Mosquirix进行了系统的文献检索; RTS,S;疟疾;疫苗;和MEDLINE(1948年-2011年11月),EMBASE(1980年-2011年11月),International Pharmaceutical Abstracts(1970年-2011年11月),Google和Google Scholar中的疟原虫。研究选择和数据提取:审查了描述疫苗开发,药理学,药代动力学,功效和安全性的临床试验。为了疗效,回顾了报道患有疟疾疾病的临床试验。提取了有关研究设计,人群,研究时间,基线特征,临床结果,结果和质量评估者的信息。数据综合:确定了五项随机对照试验和四项后续扩展研究。在2期试验中,预防第一次临床疾病发作的婴儿疫苗有效率为33-65%,儿童疫苗有效率为30-53%。在3期试验中,在5-17个月大的儿童中,疫苗效力为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的疟疾。疫苗疗效的随访期为6到45个月。 RTS,S 25μg作为婴儿和儿童的1个月间隔3次注射肌注。 RTS,S似乎普遍具有良好的耐受性。据报道有几例脑膜炎和癫痫发作(接种后7天内)。结论:RTS,S已在第1、2和3期试验中证明了疗效和安全性,并且有可能降低全世界疟疾的发病率和死亡率。主要挑战包括确定免疫的持续时间,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。尚待进一步研究,RTS,S有可能成为基准,成为首个抗疟疾的有效疫苗。

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