Krylova Yu S, Dokhov M A, Panfilova A S, Vinogradova T I, Mokrousov I V, Kvetnoy I M
St. Petersburg Research Institute of Phthisiopulmonology, St. Petersburg, Russia.
Pavlov First Saint Petersburg State Medical University, St. Petersburg, Russia.
Arkh Patol. 2024;86(4):31-37. doi: 10.17116/patol20248604131.
More than a quarter of the world's population is infected with . However, only about 10% of those infected develop active TB. This indicates a key role for innate immunity in limiting M. tuberculosis replication. Most often, bacteria can regulate the expression of host-specific molecules and weaken host immunity.
To use a biological model, in order to determine significant molecular immunohistochemical markers characterizing the virulence of the "Buryat" and "Omsk" subtypes of the Beijing genotype in lung tissue.
Lung samples of the C57BL/6 male mice were obtained during experimental infection with M. tuberculosis strains: the reference laboratory strain H37Rv, multidrug-resistant clinical strains 396 (highly lethal and hypervirulent «Buryat» genotype Beijing 14717-15) and 6691 (low-lethal and low-virulent "Omsk" genotype Beijing 1071-32) on days 14, 21, 60 and 120. They were studied by histological and immunohistochemical methods. The relative areas of expression of IL-6, IL-12A, iNOS, and TNF- in the lung tissue of model animals were established.
A study of strain 396 showed that both disease progression and damage to lung tissue are associated with a highly reactive immune response and increased synthesis of iNOS and strain characteristics that block the production of TNF-. On the contrary, for strain 6691 a low reactivity of the immune response was revealed, with statistically significantly lower values of the relative area of expression of NOS and TNF- during all observation periods (days 14-120). All animals that survived to day 120 showed a similar morphological picture with differences in cytokine levels, indicating a nonlinear relationship between proinflammatory factors and the damage substratum.
The progression of the disease and damage of lung tissue were associated with a highly reactive immune response and increased synthesis of iNOS, strain properties that block the TNF- production. Thus, iNOS and TNF- can act as molecular markers characterizing the virulence of the "Buryat" and "Omsk" subtypes of M. tuberculosis in lung tissue.
世界上超过四分之一的人口感染了[病原体名称未给出]。然而,只有约10%的感染者会发展为活动性肺结核。这表明先天免疫在限制结核分枝杆菌复制中起关键作用。大多数情况下,细菌可调节宿主特异性分子的表达并削弱宿主免疫力。
使用生物模型,以确定表征北京基因型“布里亚特”和“鄂木斯克”亚型在肺组织中毒力的重要分子免疫组化标志物。
在C57BL/6雄性小鼠实验感染结核分枝杆菌菌株期间获取肺样本:参考实验室菌株H37Rv、耐多药临床菌株396(高致死性和高毒力的“布里亚特”基因型北京14717 - 15)和6691(低致死性和低毒力的“鄂木斯克”基因型北京1071 - 32),分别在第14、21、60和120天获取样本。通过组织学和免疫组化方法对其进行研究。确定模型动物肺组织中IL - 6、IL - 12A、iNOS和TNF - 的相对表达面积。
对菌株396的研究表明,疾病进展和肺组织损伤均与高反应性免疫反应以及iNOS合成增加和阻断TNF - 产生的菌株特性有关。相反,对于菌株6691,发现免疫反应的反应性较低,在所有观察期(第14 - 120天),NOS和TNF - 的相对表达面积值在统计学上显著较低。所有存活至第120天的动物均呈现相似的形态学表现,但细胞因子水平存在差异,表明促炎因子与损伤基质之间存在非线性关系。
疾病进展和肺组织损伤与高反应性免疫反应以及iNOS合成增加、阻断TNF - 产生的菌株特性有关。因此,iNOS和TNF - 可作为表征结核分枝杆菌“布里亚特”和“鄂木斯克”亚型在肺组织中毒力的分子标志物。