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- Publisher Website: 10.1016/j.antiviral.2018.05.007
- Scopus: eid_2-s2.0-85047058929
- WOS: WOS:000437046700010
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Article: Effect of interferon alpha and cyclosporine treatment separately and in combination on Middle East Respiratory Syndrome Coronavirus (MERS-CoV) replication in a human in-vitro and ex-vivo culture model
Title | Effect of interferon alpha and cyclosporine treatment separately and in combination on Middle East Respiratory Syndrome Coronavirus (MERS-CoV) replication in a human in-vitro and ex-vivo culture model |
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Authors | |
Keywords | Cyclosporine Ex vivo explants Middle East Respiratory Syndrome Coronavirus (MERS-CoV) Type I interferon |
Issue Date | 2018 |
Citation | Antiviral Research, 2018, v. 155, p. 89-96 How to Cite? |
Abstract | Middle East Respiratory Syndrome Coronavirus (MERS-CoV) has emerged as a coronavirus infection of humans in the past 5 years. Though confined to certain geographical regions of the world, infection has been associated with a case fatality rate of 35%, and this mortality may be higher in ventilated patients. As there are few readily available animal models that accurately mimic human disease, it has been a challenge to ethically determine what optimum treatment strategies can be used for this disease. We used in-vitro and human ex-vivo explant cultures to investigate the effect of two immunomodulatory agents, interferon alpha and cyclosporine, singly and in combination, on MERS-CoV replication. In both culture systems the combined treatment was more effective than either agent used alone in reducing MERS-CoV replication. PCR SuperArray analysis showed that the reduction of virus replication was associated with a greater induction of interferon stimulated genes. As these therapeutic agents are already licensed for clinical use, it may be relevant to investigate their use for therapy of human MERS-CoV infection. |
Persistent Identifier | http://hdl.handle.net/10722/258395 |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | LI, HS | - |
dc.contributor.author | Kuok, IT | - |
dc.contributor.author | Cheung, MC | - |
dc.contributor.author | NG, MT | - |
dc.contributor.author | Ng, KC | - |
dc.contributor.author | Hui, PY | - |
dc.contributor.author | Peiris, JSM | - |
dc.contributor.author | Chan, MCW | - |
dc.contributor.author | Nicholls, JM | - |
dc.date.accessioned | 2018-08-22T01:37:47Z | - |
dc.date.available | 2018-08-22T01:37:47Z | - |
dc.date.issued | 2018 | - |
dc.identifier.citation | Antiviral Research, 2018, v. 155, p. 89-96 | - |
dc.identifier.uri | http://hdl.handle.net/10722/258395 | - |
dc.description.abstract | Middle East Respiratory Syndrome Coronavirus (MERS-CoV) has emerged as a coronavirus infection of humans in the past 5 years. Though confined to certain geographical regions of the world, infection has been associated with a case fatality rate of 35%, and this mortality may be higher in ventilated patients. As there are few readily available animal models that accurately mimic human disease, it has been a challenge to ethically determine what optimum treatment strategies can be used for this disease. We used in-vitro and human ex-vivo explant cultures to investigate the effect of two immunomodulatory agents, interferon alpha and cyclosporine, singly and in combination, on MERS-CoV replication. In both culture systems the combined treatment was more effective than either agent used alone in reducing MERS-CoV replication. PCR SuperArray analysis showed that the reduction of virus replication was associated with a greater induction of interferon stimulated genes. As these therapeutic agents are already licensed for clinical use, it may be relevant to investigate their use for therapy of human MERS-CoV infection. | - |
dc.language | eng | - |
dc.relation.ispartof | Antiviral Research | - |
dc.subject | Cyclosporine | - |
dc.subject | Ex vivo explants | - |
dc.subject | Middle East Respiratory Syndrome Coronavirus (MERS-CoV) | - |
dc.subject | Type I interferon | - |
dc.title | Effect of interferon alpha and cyclosporine treatment separately and in combination on Middle East Respiratory Syndrome Coronavirus (MERS-CoV) replication in a human in-vitro and ex-vivo culture model | - |
dc.type | Article | - |
dc.identifier.email | Cheung, MC: bccmc@hku.hk | - |
dc.identifier.email | Ng, KC: kckachun@hku.hk | - |
dc.identifier.email | Hui, PY: kenrie@hku.hk | - |
dc.identifier.email | Peiris, JSM: malik@hkucc.hku.hk | - |
dc.identifier.email | Chan, MCW: mchan@hku.hk | - |
dc.identifier.email | Nicholls, JM: jmnichol@hkucc.hku.hk | - |
dc.identifier.authority | Hui, PY=rp02149 | - |
dc.identifier.authority | Peiris, JSM=rp00410 | - |
dc.identifier.authority | Chan, MCW=rp00420 | - |
dc.identifier.authority | Nicholls, JM=rp00364 | - |
dc.identifier.doi | 10.1016/j.antiviral.2018.05.007 | - |
dc.identifier.scopus | eid_2-s2.0-85047058929 | - |
dc.identifier.hkuros | 286583 | - |
dc.identifier.volume | 155 | - |
dc.identifier.spage | 89 | - |
dc.identifier.epage | 96 | - |
dc.identifier.isi | WOS:000437046700010 | - |