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基于恶性疟原虫子孢子(PfSPZ)的疟疾疫苗研究进展。

Progress with Plasmodium falciparum sporozoite (PfSPZ)-based malaria vaccines.

作者信息

Richie Thomas L, Billingsley Peter F, Sim B Kim Lee, James Eric R, Chakravarty Sumana, Epstein Judith E, Lyke Kirsten E, Mordmüller Benjamin, Alonso Pedro, Duffy Patrick E, Doumbo Ogobara K, Sauerwein Robert W, Tanner Marcel, Abdulla Salim, Kremsner Peter G, Seder Robert A, Hoffman Stephen L

机构信息

Sanaria Inc., Rockville, MD, United States.

Sanaria Inc., Rockville, MD, United States.

出版信息

Vaccine. 2015 Dec 22;33(52):7452-61. doi: 10.1016/j.vaccine.2015.09.096. Epub 2015 Nov 27.

Abstract

Sanaria Inc. has developed methods to manufacture, purify and cryopreserve aseptic Plasmodium falciparum (Pf) sporozoites (SPZ), and is using this platform technology to develop an injectable PfSPZ-based vaccine that provides high-grade, durable protection against infection with Pf malaria. Several candidate vaccines are being developed and tested, including PfSPZ Vaccine, in which the PfSPZ are attenuated by irradiation, PfSPZ-CVac, in which fully infectious PfSPZ are attenuated in vivo by concomitant administration of an anti-malarial drug, and PfSPZ-GA1, in which the PfSPZ are attenuated by gene knockout. Forty-three research groups in 15 countries, organized as the International PfSPZ Consortium (I-PfSPZ-C), are collaborating to advance this program by providing intellectual, clinical, and financial support. Fourteen clinical trials of these products have been completed in the USA, Europe and Africa, two are underway and at least 12 more are planned for 2015-2016 in the US (four trials), Germany (2 trials), Tanzania, Kenya, Mali, Burkina Faso, Ghana and Equatorial Guinea. Sanaria anticipates application to license a first generation product as early as late 2017, initially to protect adults, and a year later to protect all persons >6 months of age for at least six months. Improved vaccine candidates will be advanced as needed until the following requirements have been met: long-term protection against natural transmission, excellent safety and tolerability, and operational feasibility for population-wide administration. Here we describe the three most developed whole PfSPZ vaccine candidates, associated clinical trials, initial plans for licensure and deployment, and long-term objectives for a final product suitable for mass administration to achieve regional malaria elimination and eventual global eradication.

摘要

Sanaria公司已研发出制造、纯化和冷冻保存无菌恶性疟原虫(Pf)子孢子(SPZ)的方法,并正利用这一平台技术来开发一种基于注射用PfSPZ的疫苗,该疫苗可提供针对Pf疟疾感染的高级别、持久保护。目前正在研发和测试几种候选疫苗,包括经辐照减毒的PfSPZ疫苗、通过同时给予抗疟药物在体内减毒的完全感染性PfSPZ的PfSPZ-CVac,以及通过基因敲除减毒的PfSPZ-GA1。作为国际PfSPZ联盟(I-PfSPZ-C),来自15个国家的43个研究小组正在通过提供智力、临床和资金支持来合作推进该项目。这些产品已在美国、欧洲和非洲完成了14项临床试验,两项正在进行中,并且计划在2015 - 2016年在美国(四项试验)、德国(两项试验)、坦桑尼亚、肯尼亚、马里、布基纳法索、加纳和赤道几内亚至少再开展12项试验。Sanaria预计最早在2017年末申请第一代产品的许可,最初用于保护成年人,一年后用于保护所有6个月以上的人群至少6个月。将根据需要推进改进的候选疫苗,直到满足以下要求:针对自然传播的长期保护、出色的安全性和耐受性,以及在人群中广泛接种的操作可行性。在此,我们描述三种研发程度最高的全PfSPZ候选疫苗、相关临床试验、许可和部署的初步计划,以及适合大规模接种以实现区域疟疾消除和最终全球根除的最终产品的长期目标。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5053/5077156/5b977a4b9256/nihms821274f1.jpg

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