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在预防性抗生素治疗可及性增加的时代进行结核病疫苗的临床试验。

Clinical trials of tuberculosis vaccines in the era of increased access to preventive antibiotic treatment.

机构信息

Institute for Global Health and MRC Clinical Trials Unit, University College London, London, UK; Wellcome Centre for Infectious Diseases Research in Africa (CIDRI-Africa), Institute of Infectious Disease and Molecular Medicine, and School of Public Health, University of Cape Town, Cape Town, South Africa; Aurum Institute, Parktown, South Africa.

Treatment Action Group, New York, NY, USA.

出版信息

Lancet Respir Med. 2023 Apr;11(4):380-390. doi: 10.1016/S2213-2600(23)00084-X. Epub 2023 Mar 23.

Abstract

Approximately 10·6 million people worldwide develop tuberculosis each year, representing a failure in epidemic control that is accentuated by the absence of effective vaccines to prevent infection or disease in adolescents and adults. Without effective vaccines, tuberculosis prevention has relied on testing for Mycobacterium tuberculosis infection and treating with antibiotics to prevent progression to tuberculosis disease, known as tuberculosis preventive treatment (TPT). Novel tuberculosis vaccines are in development and phase 3 efficacy trials are imminent. The development of effective, shorter, and safer TPT regimens has broadened the groups eligible for TPT beyond people with HIV and child contacts of people with tuberculosis; future vaccine trials will be undertaken in an era of increased TPT access. Changes in the prevention standard will have implications for tuberculosis vaccine trials of disease prevention, for which safety and sufficient accrual of cases are crucial. In this paper, we examine the urgent need for trials that allow the evaluation of new vaccines and fulfil the ethical duty of researchers to provide TPT. We observe how HIV vaccine trials have incorporated preventive treatment in the form of pre-exposure prophylaxis, propose trial designs that integrate TPT, and summarise considerations for each design in terms of trial validity, efficiency, participant safety, and ethics.

摘要

全球每年约有 1060 万人罹患结核病,这表明在控制疫情方面存在失败,而青少年和成年人缺乏有效的疫苗来预防感染或疾病,这一失败更加凸显。如果没有有效的疫苗,结核病预防就依赖于检测结核分枝杆菌感染,并使用抗生素来预防发展为结核病,即结核病预防性治疗(TPT)。新型结核病疫苗正在研发中,第 3 期疗效试验即将进行。有效的、更短的、更安全的 TPT 方案的发展扩大了 TPT 的适用人群,不仅包括艾滋病毒感染者和结核病患者的儿童接触者,未来的疫苗试验将在 TPT 可及性增加的时代进行。预防标准的改变将对结核病疫苗预防疾病的试验产生影响,因为安全性和足够的病例积累对于这些试验至关重要。在本文中,我们探讨了进行试验的迫切需要,这些试验允许评估新疫苗,并履行研究人员提供 TPT 的道德责任。我们观察了艾滋病毒疫苗试验如何将预防性治疗(以暴露前预防为形式)纳入其中,提出了整合 TPT 的试验设计,并就每种设计在试验有效性、效率、参与者安全性和伦理学方面的考虑进行了总结。

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