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疟疾疫苗佐剂:临床前和临床研究的最新进展和挑战。

Malaria vaccine adjuvants: latest update and challenges in preclinical and clinical research.

机构信息

NanoBioCel Group, Laboratory of Pharmaceutics, School of Pharmacy, University of the Basque Country (UPV/EHU), Vitoria-Gasteiz, Spain.

出版信息

Biomed Res Int. 2013;2013:282913. doi: 10.1155/2013/282913. Epub 2013 Apr 23.

DOI:10.1155/2013/282913
PMID:23710439
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3655447/
Abstract

There is no malaria vaccine currently available, and the most advanced candidate has recently reported a modest 30% efficacy against clinical malaria. Although many efforts have been dedicated to achieve this goal, the research was mainly directed to identify antigenic targets. Nevertheless, the latest progresses on understanding how immune system works and the data recovered from vaccination studies have conferred to the vaccine formulation its deserved relevance. Additionally to the antigen nature, the manner in which it is presented (delivery adjuvants) as well as the immunostimulatory effect of the formulation components (immunostimulants) modulates the immune response elicited. Protective immunity against malaria requires the induction of humoral, antibody-dependent cellular inhibition (ADCI) and effector and memory cell responses. This review summarizes the status of adjuvants that have been or are being employed in the malaria vaccine development, focusing on the pharmaceutical and immunological aspects, as well as on their immunization outcomings at clinical and preclinical stages.

摘要

目前尚无疟疾疫苗,最近最先进的候选疫苗对临床疟疾的疗效仅为 30%。尽管人们为此付出了很多努力,但研究主要集中在识别抗原靶点上。然而,最近在了解免疫系统如何运作方面的进展以及从疫苗研究中获得的数据,使疫苗的配方得到了应有的重视。除了抗原性质外,其呈现方式(传递佐剂)以及配方成分的免疫刺激作用(免疫刺激剂)也会调节所引起的免疫反应。针对疟疾的保护性免疫需要诱导体液、抗体依赖的细胞抑制(ADCI)以及效应和记忆细胞反应。本文综述了已用于或正在用于疟疾疫苗开发的佐剂的现状,重点介绍了其在药物和免疫学方面的情况,以及在临床和临床前阶段的免疫接种结果。

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本文引用的文献

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A phase 3 trial of RTS,S/AS01 malaria vaccine in African infants.RTS,S/AS01 疟疾疫苗在非洲婴儿中的 3 期临床试验。
N Engl J Med. 2012 Dec 13;367(24):2284-95. doi: 10.1056/NEJMoa1208394. Epub 2012 Nov 9.
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Phase 1 study in malaria naïve adults of BSAM2/Alhydrogel®+CPG 7909, a blood stage vaccine against P. falciparum malaria.BSAM2/Alhydrogel®+CPG 7909 在无疟疾既往史的成年人中的 1 期研究,该疫苗针对恶性疟原虫疟疾的红内期。
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Clinical assessment of a recombinant simian adenovirus ChAd63: a potent new vaccine vector.临床评估重组猿猴腺病毒 ChAd63:一种有效的新型疫苗载体。
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Combination of immune stimulating adjuvants with poly(lactide-co-glycolide) microspheres enhances the immune response of vaccines.免疫佐剂与聚(丙交酯-乙交酯)微球的结合增强了疫苗的免疫应答。
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