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[疟疾疫苗接种。失望与希望]

[Vaccination against malaria. Disappointments and hopes].

作者信息

Ambroise-Thomas P

机构信息

Département Relations Hôte-Agents Pathogènes-UPRES-A, CNRS 5082, Faculté de Médecine, Université Joseph Fourier, Grenoble.

出版信息

Bull Acad Natl Med. 1997 Nov;181(8):1637-48; discussion 1648-50.

PMID:9554123
Abstract

After the first in vitro cultivation of Plasmodium falciparum 21 years ago, the prospect of anti-malarial vaccination arose many hopes, but, in the end, it so far has mainly given rise to doubts and disappointments. Technically, the problem is particularly difficult. Plasmodium falciparum has a very complex antigenic structure with several hundreds, if not several thousands, of different epitopes for each of the four main evolutive stages of the parasite (sporozoites, merozoites, gametocytes, ookinetes) which correspond to different phase of the infection and could be a target for vaccination. Many of these epitopes are stage-specific and some of them vary from one strain to another. Adjuvants also play a major role and can qualitatively modify the type of immune response. The immune mechanisms also differ according to the final goal: anti-Plasmodium infection or anti-disease vaccine. Over the last few years, the first clinical assays have been carried out with the Spf66 vaccine, a synthetic complex protein directed against sporozoites and merozoites. In adults and children, the first results in South America and in East Africa were modest but encouraging. Unfortunately they were not confirmed by further studies in West Africa and South-East Asia. Two new types of vaccines are under preliminary clinical evaluation. One is directed against ookinetes of Plasmodium falciparum (Pfs25 and Pfs28) and can stop the transmission from the mosquito. The other is an anti-sporozoite vaccine with a new immunogen (RTS,S) in which the circumsporozoite protein is fused to the hepatitis B surface antigen and can protect against infestation. New prospects and improvements are offered by the technique of DNA vaccines and will probably also result from better knowledge of cellular and molecular biology of the parasite which is being extensively studied (genomic structure). If new promising perspectives exist, it is particularly important to be careful to avoid such disappointments as those caused, in the past, by a too-optimistic and over-publicized presentation of some preliminary results. It is now certain that one or several malaria-vaccines will be available, but no one can seriously say when, for whom and how. In any case, it is unrealistic to hope that vaccine(s) alone will be able to eradicate such an epidemiologically complex disease as malaria. It is probable that only the coordinated use of all the techniques available (anti-vectorial protection and fight, chemoprophylaxis and chemotherapy, vaccination) will lead to success.

摘要

21年前恶性疟原虫首次实现体外培养后,抗疟疾疫苗的前景带来了诸多希望,但最终,到目前为止它主要引发的是怀疑和失望。从技术层面讲,这个问题特别棘手。恶性疟原虫具有非常复杂的抗原结构,在寄生虫的四个主要发育阶段(子孢子、裂殖子、配子体、动合子)中,每个阶段都有数百个甚至数千个不同的表位,这些表位对应感染的不同阶段,可能成为疫苗接种的靶点。其中许多表位具有阶段特异性,而且有些表位因菌株不同而有所差异。佐剂也起着重要作用,并且能够在质量上改变免疫反应的类型。免疫机制也因最终目标而异:是抗疟原虫感染疫苗还是抗疾病疫苗。在过去几年里,已经对Spf66疫苗进行了首次临床试验,这是一种针对子孢子和裂殖子的合成复合蛋白。在成人和儿童中,在南美洲和东非取得的初步结果虽不显著但令人鼓舞。不幸的是,在西非和东南亚进行的进一步研究并未证实这些结果。有两种新型疫苗正在进行初步临床评估。一种针对恶性疟原虫的动合子(Pfs25和Pfs28),能够阻止蚊子传播。另一种是带有新免疫原(RTS,S)的抗子孢子疫苗,其中环子孢子蛋白与乙肝表面抗原融合,能够预防感染。DNA疫苗技术带来了新的前景和改进,对寄生虫细胞和分子生物学(基因组结构)的更深入了解可能也会带来同样的结果。如果存在新的有前景的方向,特别重要的是要谨慎避免重蹈过去因对一些初步结果过于乐观且过度宣传而导致失望的覆辙。现在可以确定的是,将会有一种或几种疟疾疫苗问世,但没人能确切说出何时、针对何人以及以何种方式推出。无论如何,仅靠疫苗就能根除像疟疾这样流行病学情况复杂的疾病,这种想法是不现实的。很可能只有综合运用所有可用技术(抗媒介防护与防治、化学预防与化疗、疫苗接种)才能取得成功。

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