Uranga Santiago, Marinova Dessislava, Martin Carlos, Pardo Julián, Aguilo Nacho
Grupo de Genética de Micobacterias, Dpto. Microbiología, Medicina Preventiva y Salud Pública, Universidad de Zaragoza, C/ Domingo Miral s/n, 50009, Zaragoza, Spain.
CIBER Enfermedades Respiratorias, Instituto de Salud Carlos III, Madrid, Spain.
PLoS One. 2016 Apr 7;11(4):e0153028. doi: 10.1371/journal.pone.0153028. eCollection 2016.
Granzyme A, a serine protease expressed in the granules of cytotoxic T and Natural Killer cells, is involved in the generation of pro-inflammatory cytokines by macrophages. Granzyme A has been described to induce in macrophages in vitro the activation of pro-inflammatory pathways that impair intracellular mycobacterial replication. In the present study, we explored the physiological relevance of Granzyme A in the control of pulmonary Mycobacterium tuberculosis infection in vivo. Our results show that, even though Granzyme A is expressed by cytotoxic cells from mouse lungs during pulmonary infection, its deficiency in knockout mice does not have an effect in the control of M. tuberculosis infection. In addition our findings indicate that absence of Granzyme A does not affect the protection conferred by the live-attenuated M. tuberculosis vaccine MTBVAC. Altogether, our findings are in apparent contradiction with previously published in vitro results and suggest that Granzyme A does not have a crucial role in vivo in the protective response to tuberculosis.
颗粒酶A是一种在细胞毒性T细胞和自然杀伤细胞的颗粒中表达的丝氨酸蛋白酶,它参与巨噬细胞促炎细胞因子的产生。颗粒酶A已被描述为在体外可诱导巨噬细胞中促炎途径的激活,从而损害细胞内分枝杆菌的复制。在本研究中,我们探讨了颗粒酶A在体内控制肺部结核分枝杆菌感染中的生理相关性。我们的结果表明,尽管在肺部感染期间颗粒酶A由小鼠肺部的细胞毒性细胞表达,但敲除小鼠中该酶的缺乏对结核分枝杆菌感染的控制没有影响。此外,我们的研究结果表明,颗粒酶A的缺失并不影响减毒活结核分枝杆菌疫苗MTBVAC所提供的保护作用。总之,我们的研究结果与先前发表的体外研究结果明显矛盾,并表明颗粒酶A在体内对结核病的保护性反应中没有关键作用。