da Costa Adeliane Castro, Nogueira Sarah Veloso, Kipnis André, Junqueira-Kipnis Ana Paula
Department of Microbiology, Immunology, Parasitology and Pathology, Instituto de Patologia Tropical e Saúde Pública, Universidade Federal de Goiás , Goiânia , Brazil.
Front Immunol. 2014 Apr 7;5:152. doi: 10.3389/fimmu.2014.00152. eCollection 2014.
Bacille Calmette-Guérin (BCG), an attenuated vaccine derived from Mycobacterium bovis, is the current vaccine of choice against tuberculosis (TB). Despite its protection against active TB in children, BCG has failed to protect adults against TB infection and active disease development, especially in developing countries where the disease is endemic. Currently, there is a significant effort toward the development of a new TB vaccine. This review article aims to address publications on recombinant BCG (rBCG) published in the last 5 years, to highlight the strategies used to develop rBCG, with a focus on the criteria used to improve immunological memory and protection compared with BCG. The literature review was done in April 2013, using the key words TB, rBCG vaccine, and memory. This review discusses the BCG strains and strategies currently used for the modification of BCG, including: overexpression of Mycobacterium tuberculosis (Mtb) immunodominant antigens already present in BCG; gene insertion of immunodominant antigens from Mtb absent in the BCG vaccine; combination of introduction and overexpression of genes that are lost during the attenuation process of BCG; BCG modifications for the induction of CD8+ T-cell immune responses and cytokines expressing rBCG. Among the vaccines discussed, VPM1002, also called rBCGΔureC:hly, is currently in human clinical trials. Much progress has been made in the effort to improve BCG, with some promising candidates, but considerable work is still required to address functional long-lasting memory.
卡介苗(BCG)是一种源自牛分枝杆菌的减毒疫苗,是目前预防结核病(TB)的首选疫苗。尽管它能保护儿童预防活动性结核病,但BCG未能保护成人预防结核感染和活动性疾病的发展,尤其是在该疾病流行的发展中国家。目前,人们正在大力研发新型结核病疫苗。这篇综述文章旨在探讨过去5年发表的关于重组卡介苗(rBCG)的文献,突出用于研发rBCG的策略,重点关注与BCG相比用于改善免疫记忆和保护作用的标准。文献综述于2013年4月进行,使用的关键词为结核病、rBCG疫苗和记忆。本综述讨论了目前用于改造BCG的菌株和策略,包括:在BCG中已存在的结核分枝杆菌(Mtb)免疫显性抗原的过表达;BCG疫苗中不存在的来自Mtb的免疫显性抗原的基因插入;在BCG减毒过程中丢失的基因的引入和过表达的组合;用于诱导CD8 + T细胞免疫反应和表达细胞因子的rBCG的BCG改造。在讨论的疫苗中,VPM1002,也称为rBCGΔureC:hly,目前正在进行人体临床试验。在改进BCG的努力中已经取得了很大进展,有一些很有前景的候选疫苗,但仍需要大量工作来解决功能性长期记忆问题。