Department of Immunology, National School of Biological Sciences, National Polytechnic Institute, Mexico City, Mexico.
Neumology Unit, General Hospital of Mexico "Eduardo Liceaga", Mexico City, Mexico.
Int J Mycobacteriol. 2021 Jul-Sep;10(3):271-278. doi: 10.4103/ijmy.ijmy_134_21.
It has been reported that sera from patients with active pulmonary tuberculosis (APT) induced nuclear changes in normal neutrophils that included pyknosis, swelling, apoptosis, and production of extracellular traps (NETs). Similar changes were observed with some sera from their household contacts but not with sera from healthy, unrelated individuals. It was suggested that those sera from household contacts that induced neutrophil nuclear changes might correspond to people with subclinical tuberculosis. Thus, our experimental approach might serve to identify individuals with early, ongoing disease.
Nuclear changes in neutrophils were fully evident by 3 h of contact and beyond. Circulating mycobacterial antigens were the most likely candidates for this effect. We wanted to know whether the nuclear changes induced on neutrophils by the sera of APT patients would negatively affect the phagocytic/microbicidal ability of neutrophils exposed to APT sera for short periods.
We now provide evidence that short-term contact (30 min) with sera from patients with pulmonary tuberculosis increases several phagocytic parameters of normal neutrophils, including endocytosis, myeloperoxidase levels, production of free reactive oxygen species, phagolysosome fusion, and microbicidal activity on Staphylococcus aureus, with these effects not being observed with sera from healthy donors. We also give evidence that suggests that ESAT-6 and CFP-10 are involved in the phenomenon.
We conclude that activation is a stage that precedes lethal nuclear changes in neutrophils and suggests that autologous neutrophils must circulate in an altered state in the APT patients, thus contributing to the pathology of the disease.
据报道,来自活动性肺结核(APT)患者的血清可诱导正常中性粒细胞发生核变化,包括固缩、肿胀、凋亡和细胞外陷阱(NETs)的产生。在一些来自其家庭接触者的血清中也观察到了类似的变化,但在来自健康、无关个体的血清中没有观察到。有人提出,那些诱导中性粒细胞核变化的来自家庭接触者的血清可能对应于有亚临床结核的人。因此,我们的实验方法可能有助于识别处于早期、进行性疾病的个体。
中性粒细胞的核变化在接触后 3 小时内完全显现,并且超过 3 小时。循环分枝杆菌抗原是这种效应的最可能候选物。我们想知道 APT 患者血清诱导的中性粒细胞核变化是否会对短时间暴露于 APT 血清的中性粒细胞的吞噬/杀菌能力产生负面影响。
我们现在提供的证据表明,与肺结核患者的血清短期接触(30 分钟)会增加正常中性粒细胞的几个吞噬参数,包括内吞作用、髓过氧化物酶水平、游离活性氧的产生、吞噬溶酶体融合和金黄色葡萄球菌的杀菌活性,而这些作用在来自健康供体的血清中并未观察到。我们还提供了证据表明,ESAT-6 和 CFP-10 参与了这一现象。
我们得出的结论是,激活是中性粒细胞发生致命核变化之前的一个阶段,并表明自身中性粒细胞必须在 APT 患者中处于改变的状态下循环,从而导致疾病的病理学变化。