Novel adjuvant formulations for delivery of anti-tuberculosis vaccine candidates

被引:42
作者
Agger, Else Marie [1 ]
机构
[1] Statens Serum Inst, Dept Infect Dis Immunol, Artillerivej 5, DK-2300 Copenhagen S, Denmark
基金
美国国家卫生研究院; 欧盟地平线“2020”;
关键词
Tuberculosis; BCG boost vaccine; Dual-component adjuvants; Immunomodulators; Delivery systems; Long-term memory; Mucosal adjuvants; PAMPs; MYCOBACTERIUM-TUBERCULOSIS INFECTION; BACILLUS-CALMETTE-GUERIN; T-CELL RESPONSES; TUMOR-NECROSIS-FACTOR; C-TYPE LECTIN; PROTECTIVE IMMUNITY; CORD FACTOR; AEROSOL INFECTION; SUBUNIT VACCINE; BOVIS BCG;
D O I
10.1016/j.addr.2015.11.012
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
There is an urgent need for a new and improved vaccine against tuberculosis for controlling this disease that continues to pose a global health threat. The current research strategy is to replace the present BCG vaccine or boost BCG-immunity with subunit vaccines such as viral vectored- or protein-based vaccines. The use of recombinant proteins holds a number of production advantages including ease of scalability, but requires an adjuvant inducing cell-mediated immune responses. A number of promising novel adjuvant formulations have recently been designed and show evidence of induction of cellular immune responses in humans. A common trait of effective TB adjuvants including those already in current clinical testing is a two-component approach combining a delivery system with an appropriate immunomodulator. This review summarizes the status of current TB adjuvant research with a focus on the division of labor between delivery systems and immunomodulators. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:73 / 82
页数:10
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