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评估恶性疟原虫无性血液期疟疾疫苗临床疗效面临的挑战。

Challenges of assessing the clinical efficacy of asexual blood-stage Plasmodium falciparum malaria vaccines.

作者信息

Sheehy Susanne H, Douglas Alexander D, Draper Simon J

机构信息

The Jenner Institute; University of Oxford; Oxford, UK.

出版信息

Hum Vaccin Immunother. 2013 Sep;9(9):1831-40. doi: 10.4161/hv.25383. Epub 2013 Jun 18.

Abstract

In the absence of any highly effective vaccine candidate against Plasmodium falciparum malaria, it remains imperative for the field to pursue all avenues that may lead to the successful development of such a formulation. The development of a subunit vaccine targeting the asexual blood-stage of Plasmodium falciparum malaria infection has proven particularly challenging with only limited success to date in clinical trials. However, only a fraction of potential blood-stage vaccine antigens have been evaluated as targets, and a number of new promising candidate antigen formulations and delivery platforms are approaching clinical development. It is therefore essential that reliable and sensitive methods of detecting, or ruling out, even modest efficacy of blood-stage vaccines in small clinical trials be established. In this article we evaluate the challenges facing blood-stage vaccine developers, assess the appropriateness and limitations of various in vivo approaches for efficacy assessment and suggest future directions for the field.

摘要

在缺乏针对恶性疟原虫疟疾的任何高效候选疫苗的情况下,该领域继续探索所有可能通向成功开发此类制剂的途径仍然至关重要。事实证明,开发针对恶性疟原虫疟疾感染无性血液阶段的亚单位疫苗极具挑战性,迄今为止在临床试验中仅取得了有限的成功。然而,仅一小部分潜在的血液阶段疫苗抗原已被评估为靶点,并且一些新的有前景的候选抗原制剂和递送平台正接近临床开发阶段。因此,建立可靠且灵敏的方法来检测或排除小型临床试验中血液阶段疫苗的哪怕是适度疗效至关重要。在本文中,我们评估了血液阶段疫苗开发者面临的挑战,评估了各种体内疗效评估方法的适用性和局限性,并为该领域提出了未来的方向。

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