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疟疾疫苗:当前视角

Malaria vaccine: a current perspective.

作者信息

Sharma Shobhona, Pathak Sulabha

机构信息

Department of Biological Sciences, Tata Institute of Fundamental Research, Mumbai, India.

出版信息

J Vector Borne Dis. 2008 Mar;45(1):1-20.

Abstract

The observation that inactivated Plasmodium sporozoites could protect against malaria is about a hundred years old. However, systematic demonstration of protection using irradiated sporozoites occurred in the nineteen-sixties, providing the impetus for the development of a malaria vaccine. In 1983, the circumsporozoite protein (CSP), a major sporozoite surface antigen, became the first Plasmodium gene to be cloned, and a CSP-based vaccine appeared imminent. Today, 25 years later, we are still without an effective malaria vaccine, despite considerable information regarding the genomics and proteomics of the malaria parasites. Although clinical immunity to malaria has been well-documented in adults living in malaria endemic areas, our understanding of the host-immune responses operating in such malaria immune persons remains poor, and limits the development of immune control of the disease. Currently, several antigen and adjuvant combinations have entered clinical trials, in which efficacy against experimental sporozoite challenge and/or exposure to natural infection is evaluated. This review collates information on the recent status of the field. Unresolved challenges facing the development of a malaria vaccine are also discussed.

摘要

灭活的疟原虫子孢子可预防疟疾这一发现已有约百年历史。然而,利用辐照子孢子进行的系统性保护证明出现在20世纪60年代,为疟疾疫苗的研发提供了动力。1983年,主要子孢子表面抗原环子孢子蛋白(CSP)成为首个被克隆的疟原虫基因,基于CSP的疫苗似乎即将问世。如今,25年过去了,尽管我们掌握了大量有关疟原虫基因组学和蛋白质组学的信息,但仍没有有效的疟疾疫苗。虽然在疟疾流行地区生活的成年人中,对疟疾的临床免疫已有充分记录,但我们对这些疟疾免疫人群中宿主免疫反应的了解仍然不足,这限制了对该疾病进行免疫控制的发展。目前,几种抗原和佐剂组合已进入临床试验,评估其对实验性子孢子攻击和/或自然感染暴露的疗效。本综述整理了该领域的最新信息,还讨论了疟疾疫苗研发面临的未解决挑战。

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