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
Department of Microbiology and Immunology, Albert Einstein College of Medicine, 1300 Morris Park Avenue, Bronx, NY 10461, United States.
Vaccine. 2006 Sep 11;24(37-39):6309-20. doi: 10.1016/j.vaccine.2006.05.097. Epub 2006 Jun 12.
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 (DeltaRD1) and two genes required for the synthesis of pantothenate (DeltapanCD). The M. tuberculosis DeltaRD1 DeltapanCD (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.
在不断蔓延的艾滋病大流行的推动下,全球结核病疫情促使人们研发一种安全有效的结核病疫苗。我们报告了结核分枝杆菌H37Rv的一种非连锁双缺失突变体的构建和特性,该突变体删除了卡介苗的主要减毒突变(DeltaRD1)和泛酸合成所需的两个基因(DeltapanCD)。结核分枝杆菌DeltaRD1 DeltapanCD(mc(2)6030)突变体在小鼠体内的复制有限,但在免疫受损小鼠中比卡介苗显著更安全,在豚鼠中也安全。此外,mc(2)6030菌株在小鼠化学免疫抑制模型中不会重新激活。重要的是,用mc(2)6030菌株免疫后产生的长期保护性免疫反应可延长野生型小鼠和CD4缺陷小鼠在受到强毒结核分枝杆菌气溶胶攻击后的存活时间。鉴于其总体安全性和有效性,mc(2)6030减毒活菌株应被视为一种人类疫苗候选物,用于保护健康个体和艾滋病毒感染者免受结核病侵害。