Laporte Manon, Naesens Lieve
Rega Institute for Medical Research, Department of Microbiology and Immunology, KU Leuven, Leuven, Belgium.
Rega Institute for Medical Research, Department of Microbiology and Immunology, KU Leuven, Leuven, Belgium.
Curr Opin Virol. 2017 Jun;24:16-24. doi: 10.1016/j.coviro.2017.03.018. Epub 2017 Apr 14.
To enter into airway epithelial cells, influenza, parainfluenza- and coronaviruses rely on host cell proteases for activation of the viral protein involved in membrane fusion. One protease, transmembrane protease serine 2 (TMPRSS2) was recently proven to be crucial for hemagglutinin cleavage of some human influenza viruses. Since the catalytic sites of the diverse serine proteases linked to influenza, parainfluenza- and coronavirus activation are structurally similar, active site inhibitors of these airway proteases could have broad therapeutic applicability against multiple respiratory viruses. Alternatively, superior selectivity could be achieved with allosteric inhibitors of TMPRSS2 or another critical protease. Though still in its infancy, airway protease inhibition represents an attractive host-cell targeting approach to combat respiratory viruses such as influenza.
为进入气道上皮细胞,流感病毒、副流感病毒和冠状病毒依赖宿主细胞蛋白酶来激活参与膜融合的病毒蛋白。一种蛋白酶,跨膜蛋白酶丝氨酸2(TMPRSS2)最近被证明对某些人类流感病毒的血凝素裂解至关重要。由于与流感、副流感和冠状病毒激活相关的多种丝氨酸蛋白酶的催化位点在结构上相似,这些气道蛋白酶的活性位点抑制剂可能对多种呼吸道病毒具有广泛的治疗适用性。或者,通过TMPRSS2或另一种关键蛋白酶的变构抑制剂可以实现更高的选择性。尽管气道蛋白酶抑制仍处于起步阶段,但它是一种有吸引力的靶向宿主细胞的方法,可用于对抗流感等呼吸道病毒。