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非洲的人体疟疾感染控制研究:过去、现在和未来。

Controlled Human Malaria Infection Studies in Africa-Past, Present, and Future.

机构信息

Bioscience Department, KEMRI-Wellcome Trust Research Program, Kilifi, Kenya.

KEMRI-Wellcome Trust Research Program, Kilifi, Kenya.

出版信息

Curr Top Microbiol Immunol. 2024;445:337-365. doi: 10.1007/82_2022_256.

DOI:10.1007/82_2022_256
PMID:35704094
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7616462/
Abstract

Controlled human infection studies have contributed significantly to the understanding of pathogeneses and treatment of infectious diseases. In malaria, deliberately infecting humans with malaria parasites was used as a treatment for neurosyphilis in the early 1920s. More recently, controlled human malaria infection (CHMI) has become a valuable, cost-effective tool to fast-track the development and evaluation of new anti-malarial drugs and/or vaccines. CHMI studies have also been used to define host/parasite interactions and immunological correlates of protection. CHMI involves infecting a small number of healthy volunteers with malaria parasites, monitoring their parasitemia and providing anti-malarial treatment when a set threshold is reached. In this review we discuss the introduction, development, and challenges of modern-day Plasmodium falciparum CHMI studies conducted in Africa, and the impact of naturally acquired immunity on infectivity and vaccine efficacy. CHMIs have shown to be an invaluable tool particularly in accelerating malaria vaccine research. Although there are limitations of CHMI studies for estimating public health impacts and for regulatory purposes, their strength lies in proof-of-concept efficacy data at an early stage of development, providing a faster way to select vaccines for further development and providing valuable insights in understanding the mechanisms of immunity to malarial infection.

摘要

人体受控感染研究极大地促进了人们对传染病发病机制和治疗方法的理解。在疟疾领域,20 世纪 20 年代初,人们曾故意用疟原虫感染人体来治疗神经梅毒。最近,人体受控疟疾感染(CHMI)已成为一种有价值且具有成本效益的工具,可用于加速新抗疟药物和/或疫苗的研发和评估。CHMI 研究还被用于确定宿主/寄生虫相互作用和保护性免疫的相关因素。CHMI 涉及用疟原虫感染少数健康志愿者,在达到设定阈值时监测其疟原虫血症并提供抗疟治疗。在本文中,我们讨论了在非洲进行的现代恶性疟原虫 CHMI 研究的引入、发展和挑战,以及自然获得性免疫对传染性和疫苗效力的影响。CHMI 已被证明是一种非常有价值的工具,特别是在加速疟疾疫苗研究方面。尽管 CHMI 研究在估计公共卫生影响和监管方面存在局限性,但它们的优势在于在开发的早期阶段提供了概念验证的疗效数据,为进一步开发选择疫苗提供了更快的途径,并为理解疟疾感染免疫机制提供了有价值的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d08b/7616462/f8de9e454368/EMS153584-f002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d08b/7616462/103678423d3f/EMS153584-f001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d08b/7616462/f8de9e454368/EMS153584-f002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d08b/7616462/103678423d3f/EMS153584-f001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d08b/7616462/f8de9e454368/EMS153584-f002.jpg

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Exploratory analysis of the effect of helminth infection on the immunogenicity and efficacy of the asexual blood-stage malaria vaccine candidate GMZ2.
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