Sharan Riti, Kaushal Deepak
Southwest National Primate Center, Texas Biomedical Research Institute, San Antonio, TX 78227 USA.
NPJ Vaccines. 2020 Oct 13;5:95. doi: 10.1038/s41541-020-00245-9. eCollection 2020.
One-third of world's population is predicted to be infected with tuberculosis (TB). The resurgence of this deadly disease has been inflamed by comorbidity with human immunodeficiency virus (HIV). The risk of TB in people living with HIV (PLWH) is 15-22 times higher than people without HIV. Development of a single vaccine to combat both diseases is an ardent but tenable ambition. Studies have focused on the induction of specific humoral and cellular immune responses against HIV-1 following recombinant BCG (rBCG) expressing HIV-1 antigens. Recent advances in the TB vaccines led to the development of promising candidates such as MTBVAC, the BCG revaccination approach, H4:IC31, H56:IC31, M72/AS01 and more recently, intravenous (IV) BCG. Modification of these vaccine candidates against TB/HIV coinfection could reveal key correlates of protection in a representative animal model. This review discusses the (i) potential TB vaccine candidates that can be exploited for use as a dual vaccine against TB/HIV copandemic (ii) progress made in the realm of TB/HIV dual vaccine candidates in small animal model, NHP model, and human clinical trials (iii) the failures and promising targets for a successful vaccine strategy while delineating the correlates of vaccine-induced protection.
预计全球三分之一的人口会感染结核病(TB)。这种致命疾病因与人类免疫缺陷病毒(HIV)合并感染而再度肆虐。HIV感染者(PLWH)患结核病的风险比未感染HIV的人高15至22倍。研发一种能同时对抗这两种疾病的单一疫苗是一项热切但可行的目标。研究聚焦于在表达HIV-1抗原的重组卡介苗(rBCG)接种后诱导针对HIV-1的特异性体液免疫和细胞免疫反应。结核病疫苗的最新进展促成了一些有前景的候选疫苗的研发,如MTBVAC、卡介苗再接种方法、H4:IC31、H56:IC31、M72/AS01,以及最近的静脉注射(IV)卡介苗。对这些针对结核/艾滋病病毒合并感染的候选疫苗进行改良,可能会在具有代表性的动物模型中揭示关键的保护相关因素。本综述讨论了(i)可开发用作针对结核/艾滋病病毒大流行的双价疫苗的潜在结核病候选疫苗;(ii)在小动物模型、非人灵长类动物模型和人体临床试验中,结核/艾滋病病毒双价候选疫苗领域取得的进展;(iii)成功疫苗策略的失败之处和有前景的靶点,同时阐述疫苗诱导保护的相关因素。