Division of Infectious Diseases, Department of Internal Medicine, University of Texas Medical Branch at Galveston, Texas, USA; Department of Microbiology and Immunology, University of Texas Medical Branch at Galveston, Texas, USA.
Division of Infectious Diseases, Department of Internal Medicine, University of Texas Medical Branch at Galveston, Texas, USA.
Virology. 2019 Aug;534:80-86. doi: 10.1016/j.virol.2019.06.001. Epub 2019 Jun 10.
The immunopathological mechanisms as well as the role played by influenza A virus infection of human leukocytes and induction of apoptosis have not been fully elucidated. We confirm here that the percentage of cells that are infected is less than the percent of apoptotic cells. Depletion of monocytes/macrophages and depletion of cells expressing influenza neuraminidase from the cultures after exposure to virus decreased lymphocyte apoptosis. Treatment of virus-exposed leukocyte cultures with anti-neuraminidase antibodies but not with anti-hemagglutinin antibodies, reduced lymphocyte production of active caspase-3 and induction of apoptosis. Different strains of virus induced different levels of apoptosis. Variations in induction of apoptosis correlated with production and expression of viral neuraminidase by infected leukocytes. The data suggest that cell surface expression of neuraminidase plays an important role in the induction of apoptosis in human lymphocytes. The benefit, or cost, to the host of lymphocyte apoptosis warrants continued investigation.
流感病毒感染人白细胞的免疫病理机制以及诱导细胞凋亡的作用尚未完全阐明。我们在此证实,感染的细胞百分比小于凋亡细胞的百分比。在暴露于病毒后,从培养物中去除单核细胞/巨噬细胞和表达流感神经氨酸酶的细胞可减少淋巴细胞凋亡。用抗神经氨酸酶抗体而非抗血凝素抗体处理病毒暴露的白细胞培养物可减少淋巴细胞产生活性半胱天冬酶-3并诱导凋亡。不同株病毒诱导的凋亡水平不同。凋亡诱导的变化与感染白细胞中病毒神经氨酸酶的产生和表达相关。数据表明,细胞表面神经氨酸酶的表达在诱导人淋巴细胞凋亡中发挥重要作用。淋巴细胞凋亡对宿主的益处或代价值得进一步研究。