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Cleavage of the viral surface glycoprotein hemagglutinin (HA) by host proteases is a prerequisite for membrane fusion and essential for virus infectivity. Inhibition of relevant proteases provides a promising therapeutic approach that may avoid the development of drug resistance. HA of most influenza viruses is cleaved at a monobasic cleavage site, and a number of proteases have been shown to cleave HA\n            <jats:italic>in vitro<\/jats:italic>\n            . This study demonstrates that the transmembrane protease TMPRSS2 is the major HA-activating protease of IAV in primary human bronchial cells and of both IAV and IBV in primary human type II pneumocytes. It further reveals that human and murine airway cells can differ in their HA-cleaving protease repertoires. Our data will help drive the development of potent and selective protease inhibitors as novel drugs for influenza treatment.\n          <\/jats:p>","DOI":"10.1128\/jvi.00649-19","type":"journal-article","created":{"date-parts":[[2019,8,6]],"date-time":"2019-08-06T13:22:33Z","timestamp":1565097753000},"update-policy":"https:\/\/doi.org\/10.1128\/asmj-crossmark-policy-page","source":"Crossref","is-referenced-by-count":168,"title":["TMPRSS2 Is the Major Activating Protease of Influenza A Virus in Primary Human Airway Cells and Influenza B Virus in Human Type II Pneumocytes"],"prefix":"10.1128","volume":"93","author":[{"given":"Hannah","family":"Limburg","sequence":"first","affiliation":[{"name":"Institute of Virology, Philipps University, Marburg, Germany"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Anne","family":"Harbig","sequence":"additional","affiliation":[{"name":"Institute of Virology, Philipps University, Marburg, 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