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潜伏相关抗原对结核分枝杆菌的免疫原性。

Immunogenic potential of latency associated antigens against Mycobacterium tuberculosis.

机构信息

DS Kothari Centre for Research and Innovation in Science Education, Miranda House, University of Delhi, Delhi 110007, India.

出版信息

Vaccine. 2014 Feb 3;32(6):712-6. doi: 10.1016/j.vaccine.2013.11.065. Epub 2013 Dec 2.

Abstract

Tuberculosis remains a great health threat to the world among infectious diseases particularly with the advent of human immunodeficiency virus and emergence of drug resistant strains. In the light of the inconsistent efficacy imparted by the only currently available pre-exposure vaccine bacillus Calmette-Guerin BCG, the development of an improved TB vaccine is a very high international research priority. Vaccine candidates currently in clinical trials are also pre-exposure vaccines that aim to prevent active tuberculosis during an individual's lifetime. According to World Health Organization approximately a third of the world's population is latently infected with Mycobacterium tuberculosis. Dormancy or latency of Mycobacteria is associated with the formation of granuloma with poorly perfused interior leading to expression of genes which help them survive in this hostile environment. A group of about 50 genes belonging to the DosR regulon also known as latency antigens are expressed by Mycobacteria when they are persisting in the immuno-competent host. An understanding of the immunological effects produced by products of these latency induced genes may help in making a more potent vaccine. Incorporation of latency antigens into improved (live or subunit) vaccines may enhance the impact of these vaccines in which BCG priming can be followed by multisubunit protein boosting. These vaccines could act as post exposure vaccines for containment and prevention of latent TB activation. This heterologous boosting of BCG-primed immunity will be able to stimulate the known immune correlates of protective immunity against M. tuberculosis i.e. TH1 cells (CD4(+) and CD8(+) T cells) mediated immune responses with cytokines such as IFN-γ and TNF-α⋅ In our review we have analysed and compared the immunogenic potential of various latency-associated antigens of the DosR regulon in line with the current strategy of developing a recombinant post exposure booster vaccine.

摘要

结核病仍然是世界上传染病的一大健康威胁,尤其是随着人类免疫缺陷病毒的出现和耐药菌株的出现。鉴于目前唯一可用的预防性疫苗卡介苗(BCG)的效果不一致,因此开发一种改良的结核病疫苗是一个非常高的国际研究重点。目前正在临床试验中的疫苗候选物也是预防性疫苗,旨在预防个体一生中的活动性结核病。根据世界卫生组织的数据,世界上大约有三分之一的人口感染了结核分枝杆菌。分枝杆菌的休眠或潜伏与形成肉芽肿有关,内部灌注不良,导致有助于它们在这种恶劣环境中生存的基因表达。一组约 50 个属于 DosR 调节子的基因(也称为潜伏抗原)在分枝杆菌持续存在于免疫功能正常的宿主中时被表达。了解这些潜伏诱导基因产物产生的免疫效应可能有助于制造更有效的疫苗。将潜伏抗原纳入改良的(活疫苗或亚单位疫苗)中可能会增强这些疫苗的效果,其中 BCG 初免后可以进行多亚单位蛋白加强。这些疫苗可以作为接触后疫苗,用于控制和预防潜伏性结核病的激活。这种 BCG 初免免疫的异源增强将能够刺激针对 M. tuberculosis 的保护性免疫的已知免疫相关性,即 TH1 细胞(CD4(+)和 CD8(+) T 细胞)介导的免疫反应,伴随 IFN-γ和 TNF-α等细胞因子。在我们的综述中,我们根据开发重组接触后增强疫苗的当前策略,分析和比较了 DosR 调节子的各种潜伏相关抗原的免疫原性潜力。

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