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Addressing the bottleneck at clinical testing of candidate malaria vaccines

机译:解决候选疟疾疫苗临床测试的瓶颈

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[Extract] Invited Commentary on 'Preerythrocytic and Blood-Stage Malaria Vaccines Can Be Assessed in Small Sporozoite Challenge Trials in Human Volunteers', Roestenberg et al., Journal of Infectious Diseases, 2012.\ud\udVaccines are a very effective health care intervention but are not available for many diseases, including malaria. Potential candidates have been identified in preclinical research studies and some have progressed through preclinical development to clinical trials (http://www.who.int/vaccine_research/links/Rainbow/en/index.html). However, the vaccine development pathway is long and expensive and there is a major bottleneck at the stage of clinical testing. For malaria, only a single candidate has advanced to Phase 3.1 Agnandji ST, Lell B, Soulanoudjingar SS, Fernandes JF, Abossolo BP, Conzelmann C, et al.. RTS,S Clinical Trials Partnership. First results of phase 3 trial of RTS,S/AS01 malaria vaccine in African children. N Engl J Med. 2011;365(20):1863–75. Moreover, rodent malaria models exist but protection against challenge with the causative parasites of human malaria can only be assessed in humans, and there are no known correlates of protective immunity to malaria. Candidate vaccines that fail to meet defined go/no-go criteria in animals during development may nonetheless exhibit efficacy in humans. The testing of a larger portfolio of vaccine candidates in small numbers of volunteers in clinical research studies would be valuable.
机译:[摘录]关于“可以在人类志愿者的小型子孢子挑战试验中评估促红细胞生成和血期疟疾疫苗的特邀评论”,Roestenberg等人,《传染病杂志》,2012年。\ ud \ ud疫苗是一种非常有效的保健干预措施但不适用于多种疾病,包括疟疾。在临床前研究中已经确定了潜在的候选药物,其中一些已经从临床前研究发展到临床试验(http://www.who.int/vaccine_research/links/Rainbow/en/index.html)。然而,疫苗开发途径漫长且昂贵,并且在临床测试阶段存在主要瓶颈。对于疟疾,只有一名候选人晋升到3.1期Agnandji ST,Lell B,Soulanoudjingar SS,Fernandes JF,Abossolo BP,Conzelmann C等。RTS,S Clinical Trials Partnership。 RTS,S / AS01疟疾疫苗在非洲儿童中进行的3期试验的初步结果。 N Engl J Med。 2011; 365(20):1863-75。而且,存在啮齿动物疟疾模型,但是只能在人类中评估针对人类疟疾的致病性寄生虫的攻击的保护,并且尚无已知的针对疟疾的保护性免疫的相关性。然而,在发育过程中未能满足动物定义的合格/不合格标准的候选疫苗可能仍对人类有效。在临床研究中对少量志愿者进行更大范围的候选疫苗测试是有价值的。

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