Shi Changhong, Shi Jieran, Xu Zhikai
Division of Infection and Immunology, Research Center of Laboratory Animals, Fourth Military Medical University, 17 Changle West Road, Xi'an 710032, Shaanxi Province, China.
Scand J Infect Dis. 2011 Dec;43(11-12):848-56. doi: 10.3109/00365548.2011.603745. Epub 2011 Sep 6.
The mechanisms of latency and the causes of reactivation of Mycobacterium tuberculosis remain poorly understood; an important reason for this gap in knowledge is the absence of a standardized animal model of latent tuberculosis infection (LTBI). A complete LTBI model should incorporate 2 aspects of LTBI: a persistent infection model with a low bacterial load and a latent infection model that is modified from the Cornell model. Many parameters must be carefully considered to establish an LTBI model, including the inoculating dose, the route of infection, the time interval between infection and the initiation of antibiotic therapy, and the genetic background of the host animal. The responsiveness of this mouse model of LTBI can be assessed through the integrated use of indices, including Karnofsky performance status, bacterial load in spleen and lungs, induced levels of interferon-gamma and tumour necrosis factor-alpha, expression of interleukin (IL)-10 and IL-4 in tissues, specific antigen load in organs, time required for hormone-induced TB relapse, expression level of dormancy genes, and CD4 T-cell count.
结核分枝杆菌潜伏的机制以及再激活的原因仍未得到充分了解;知识存在这一空白的一个重要原因是缺乏标准化的潜伏性结核感染(LTBI)动物模型。一个完整的LTBI模型应包含LTBI的两个方面:细菌载量低的持续性感染模型以及从康奈尔模型改良而来的潜伏感染模型。建立一个LTBI模型必须仔细考虑许多参数,包括接种剂量、感染途径、感染与开始抗生素治疗之间的时间间隔以及宿主动物的遗传背景。这种LTBI小鼠模型的反应性可以通过综合使用多种指标来评估,这些指标包括卡诺夫斯基功能状态、脾脏和肺部的细菌载量、诱导产生的γ干扰素和肿瘤坏死因子-α水平、组织中白细胞介素(IL)-10和IL-4的表达、器官中的特异性抗原载量、激素诱导的结核病复发所需时间、休眠基因的表达水平以及CD4 T细胞计数。