Live Attenuated Vaccines against Tuberculosis: Targeting the Disruption of Genes Encoding the Secretory Proteins of Mycobacteria

被引:1
作者
Veerapandian, Raja [1 ]
Gadad, Shrikanth S. [2 ]
Jagannath, Chinnaswamy [3 ,4 ]
Dhandayuthapani, Subramanian [1 ]
机构
[1] Texas Tech Univ, Ctr Emphasis Infect Dis, Paul L Foster Sch Med, Dept Mol & Translat Med,Hlth Sci Ctr El Paso, El Paso, TX 79905 USA
[2] Texas Tech Univ, Paul L Foster Sch Med, Dept Mol & Translat Med, Ctr Emphasis Canc,Hlth Sci Ctr El Paso, El Paso, TX 79905 USA
[3] Houston Methodist Res Inst, Dept Pathol & Genom Med, Houston, TX 77030 USA
[4] Weill Cornell Med Coll, Houston, TX 77030 USA
关键词
tuberculosis; live attenuated vaccines (LAVs); gene knockout; Mycobacterium tuberculosis; BCG; secretory antigens; BACILLUS-CALMETTE-GUERIN; CELL-WALL; VII SECRETION; PHAGOSOME MATURATION; EIS PROTEIN; IN-VITRO; SUPEROXIDE-DISMUTASE; GLUTAMINE-SYNTHETASE; PROTECTIVE IMMUNITY; LIPOPROTEIN RV3763;
D O I
10.3390/vaccines12050530
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Tuberculosis (TB), a chronic infectious disease affecting humans, causes over 1.3 million deaths per year throughout the world. The current preventive vaccine BCG provides protection against childhood TB, but it fails to protect against pulmonary TB. Multiple candidates have been evaluated to either replace or boost the efficacy of the BCG vaccine, including subunit protein, DNA, virus vector-based vaccines, etc., most of which provide only short-term immunity. Several live attenuated vaccines derived from Mycobacterium tuberculosis (Mtb) and BCG have also been developed to induce long-term immunity. Since Mtb mediates its virulence through multiple secreted proteins, these proteins have been targeted to produce attenuated but immunogenic vaccines. In this review, we discuss the characteristics and prospects of live attenuated vaccines generated by targeting the disruption of the genes encoding secretory mycobacterial proteins.
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