Challenges in Developing a Controlled Human Tuberculosis Challenge Model.

3区 医学 Q2 Medicine
Susan Jackson, Helen McShane
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引用次数: 0

Abstract

Controlled human infection models (CHIMs) have provided pivotal scientific advancements, contributing to the licensure of new vaccines for many pathogens. Despite being one of the world's oldest known pathogens, there are still significant gaps in our knowledge surrounding the immunobiology of Mycobacterium tuberculosis (M. tb). Furthermore, the only licensed vaccine, BCG, is a century old and demonstrates limited efficacy in adults from endemic areas. Despite good global uptake of BCG, tuberculosis (TB) remains a silent epidemic killing 1.4 million in 2019 (WHO, Global tuberculosis report 2020). A mycobacterial CHIM could expedite the development pipeline of novel TB vaccines and provide critical understanding on the immune response to TB. However, developing a CHIM for such a complex organism is a challenging process. The first hurdle to address is which challenge agent to use, as it would not be ethical to use virulent M. tb. This chapter describes the current progress and outstanding issues in the development of a TB CHIM. Previous and current human studies include both aerosol and intradermal models using either BCG or purified protein derivative (PPD) as a surrogate agent. Future work investigating the use of attenuated M. tb is underway.

开发受控人类结核病挑战模型所面临的挑战。
受控人类感染模型(CHIMs)取得了举足轻重的科学进步,为许多病原体的新疫苗获得许可做出了贡献。尽管结核分枝杆菌(M. tb)是世界上已知的最古老的病原体之一,但我们对其免疫生物学的了解仍有很大差距。此外,唯一获得许可的卡介苗已有百年历史,对流行地区成人的疗效有限。尽管卡介苗的全球接种率很高,但结核病(TB)仍然是一种无声的流行病,2019 年将导致 140 万人死亡(世卫组织,《2020 年全球结核病报告》)。分枝杆菌 CHIM 可以加快新型结核病疫苗的开发进程,并为了解结核病的免疫反应提供重要依据。然而,为如此复杂的生物体开发 CHIM 是一个具有挑战性的过程。首先要解决的障碍是使用哪种挑战剂,因为使用毒性结核杆菌是不道德的。本章介绍了结核病 CHIM 开发的当前进展和悬而未决的问题。以往和当前的人体研究包括气溶胶和皮内模型,使用卡介苗或纯化蛋白衍生物(PPD)作为替代制剂。目前正在研究如何使用减毒结核杆菌。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
5.60
自引率
0.00%
发文量
26
审稿时长
>12 weeks
期刊介绍: The review series Current Topics in Microbiology and Immunology provides a synthesis of the latest research findings in the areas of molecular immunology, bacteriology and virology. Each timely volume contains a wealth of information on the featured subject. This review series is designed to provide access to up-to-date, often previously unpublished information.
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