Marinova Dessislava, Gonzalo-Asensio Jesus, Aguilo Nacho, Martin Carlos
a Grupo de Genética de Micobacterias, Dpto. Microbiología, Medicina Preventiva y Salud Pública , Universidad de Zaragoza , Zaragoza , Spain.
b CIBER Enfermedades Respiratorias , Instituto de Salud Carlos III , Madrid , Spain.
Expert Rev Vaccines. 2017 Jun;16(6):565-576. doi: 10.1080/14760584.2017.1324303. Epub 2017 May 12.
BCG remains the only vaccine against tuberculosis (TB) in use today and despite its impressive global coverage, the nature of BCG protection against the pulmonary forms of TB remains subject to ongoing debate. Because of the limitations of BCG, novel TB vaccine candidates have been developed and several have reached the clinical pipeline. One of these candidates is MTBVAC, the first and only TB vaccine in the clinical pipeline to date based on live-attenuated Mycobacterium tuberculosis that has successfully entered clinical evaluation, a historic milestone in human vaccinology. Areas covered: This review describes development of MTBVAC from discovery to clinical development in high burden TB-endemic countries. The preclinical experiments where MTBVAC has shown to confer improved safety and efficacy over BCG are presented and the clinical development plans for MTBVAC are revealed. The search of all supportive literature in this manuscript was carried out via Pubmed. Expert commentary: Small experimental medicine trials in humans and preclinical efficacy studies with a strong immunological component mimicking clinical trial design are considered essential by the scientific community to help identify reliable vaccine-specific correlates of protection in order to support and accelerate community-wide efficacy trials of new TB vaccines.
卡介苗仍是目前唯一使用的抗结核疫苗,尽管其在全球的接种覆盖率令人瞩目,但卡介苗对肺结核的保护作用仍存在争议。由于卡介苗存在局限性,新型结核疫苗候选物已被研发出来,其中一些已进入临床阶段。这些候选物之一是MTBVAC,它是首个也是目前临床阶段唯一基于减毒活结核分枝杆菌的结核疫苗,已成功进入临床评估,这是人类疫苗学的一个历史性里程碑。涵盖领域:本综述描述了MTBVAC从发现到在高负担结核流行国家进行临床开发的过程。介绍了MTBVAC在临床前实验中显示出比卡介苗具有更高安全性和有效性的情况,并揭示了MTBVAC的临床开发计划。本手稿中所有支持性文献的检索均通过PubMed进行。专家评论:科学界认为,在人体中进行小型实验性医学试验以及开展具有强大免疫成分且模仿临床试验设计的临床前疗效研究,对于帮助确定可靠的疫苗特异性保护相关性至关重要,以便支持和加速新型结核疫苗的全社区疗效试验。