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Pre-erythrocytic stage malaria vaccines: time for a change in path

机译:红细胞前期疟疾疫苗:改变路径的时间

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Vaccines against the pre-erythrocytic stages of malaria hold the greatest promise as an effective intervention tool against malaria, as shown by immunization with radiation-attenuated sporozoites over four decades ago. To date, however, the development of subunit vaccines, while generating high expectations and investment, has not lived up at all to the promise. This path has been characterized by insufficient research into both identification of key defense mechanisms in humans and the discovery of better antigens, focusing rather on a technological race of how to present mainly a single antigen. The lack of success has also led, perhaps from desperation, to a revival of the live attenuated sporozoite approach, handicapped, however, by major bottlenecks in production, safety, and regulatory issues. It should now be clear that the field can no longer continue to succeed in mice and fall in the clinic. We advocate here in favor of a third option, relying on an understanding of the basis of attenuated sporozoite immunity in humans, to provide leads to the discovery of critical immunogens and the use of models with validated relevance to the human situation in order to rationalize and renew the promise of pre-erythrocytic subunit vaccines.
机译:对抗疟疾的促红细胞生成前阶段的疫苗作为抗击疟疾的有效干预工具具有最大的希望,正如四十多年前用辐射减弱的子孢子进行的免疫接种所表明的那样。然而,迄今为止,亚单位疫苗的开发虽然产生了很高的期望和投资,但并未完全兑现承诺。该途径的特点是对人类关键防御机制的鉴定和更好的抗原的发现研究不足,而侧重于主要呈递单个抗原的技术竞赛。缺乏成功也可能导致绝望,导致活的子孢子减毒方法的复兴,但是由于生产,安全和监管问题的严重瓶颈而受到阻碍。现在应该清楚的是,该领域不再能够继续在小鼠中成功并落入临床。在这里,我们主张第三种选择,即依靠对人类子孢子减毒免疫基础的理解,以提供关键免疫原的发现和与人类状况相关的模型的使用,从而合理化和合理化。更新了红细胞前亚基疫苗的前景。

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