Mycobacterium tuberculosis ΔRD1 ΔpanCD:: A safe and limited replicating mutant strain that protects immunocompetent and immunocompromised mice against experimental tuberculosis

被引:157
作者
Sambandamurthy, Vasan K.
Derrick, Steven C.
Hsu, Tsungda
Chen, Bing
Larsen, Michelle H.
Jalapathy, Kripa V.
Chen, Mei
Kim, John
Porcelli, Steven A.
Chan, John
Morris, Sheldon L.
Jacobs, William R., Jr.
机构
[1] US FDA, Ctr Biol Evaluat & Res, Bethesda, MD 20892 USA
[2] Albert Einstein Coll Med, Dept Microbiol & Immunol, Bronx, NY 10461 USA
[3] Albert Einstein Coll Med, Dept Med, Bronx, NY 10461 USA
[4] Novartis Inst Trop Dis, Singapore 138670, Singapore
关键词
tuberculosis; mycobacterial vaccines; BCG; attenuated strains;
D O I
10.1016/j.vaccine.2006.05.097
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The global epidemic of tuberculosis (TB), fueled by the growing HIV pandemic, warrants the development of a safe and effective vaccine against TB. We report the construction and characterization of an unlinked double deletion mutant of Mycobacterium tuberculosis H37Rv that deletes both the primary attenuating mutation of BCG (Delta RD1) and two genes required for the synthesis of pantothenate (Delta panCD). The M. tuberculosis Delta RD1 Delta panCD (mc(2)6030) mutant undergoes limited replication in mice, and yet is both significantly safer than BCG in immunocompromised mice and also safe in guinea pigs. Additionally, the mc(2)6030 strain does not reactivate in a mouse chemo-immunosuppression model. Importantly, long-lived protective immune responses following immunization with the mc(2)6030 strain prolong the survival of wild type mice, and CD4-deficient mice against an aerosol challenge with virulent M. tuberculosis. Given its overall safety and effectiveness, the mc(2)6030 live attenuated strain should be considered as a human vaccine candidate for protecting both healthy and HIV-infected individuals against TB. (c) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:6309 / 6320
页数:12
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