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- Publisher Website: 10.3389/fimmu.2017.00210
- Scopus: eid_2-s2.0-85017204325
- PMID: 28321215
- WOS: WOS:000395545200001
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Article: IFN-λ inhibits drug-resistant HIV infection of macrophages
Title | IFN-λ inhibits drug-resistant HIV infection of macrophages |
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Authors | |
Keywords | Antiretrovirals Drug-resistant HIV IFN-λ Mx2 Tetherin |
Issue Date | 2017 |
Citation | Frontiers in Immunology, 2017, v. 8, n. MAR, article no. 210 How to Cite? |
Abstract | Type III interferons (IFN-λs) have been demonstrated to inhibit a number of viruses, including HIV. Here, we further examined the anti-HIV effect of IFN-λs in macrophages. We found that IFN-λs synergistically enhanced anti-HIV activity of antiretrovirals [azidothymidine (AZT), efavirenz, indinavir, and enfuvirtide] in infected macrophages. Importantly, IFN-λs could suppress HIV infection of macrophages with the drug-resistant strains, including AZT-resistant virus (A012) and reverse transcriptase inhibitor-resistant virus (TC49). Mechanistically, IFN-λs were able to induce the expression of several important anti-HIV cellular factors, including myxovirus resistance 2 (Mx2), a newly identified HIV post-entry inhibitor and tetherin, a restriction factor that blocks HIV release from infected cells. These observations provide additional evidence to support the potential use of IFN-λs as therapeutics agents for the treatment of HIV infection. |
Persistent Identifier | http://hdl.handle.net/10722/321723 |
PubMed Central ID | |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Wang, Xu | - |
dc.contributor.author | Wang, He | - |
dc.contributor.author | Liu, Man Qing | - |
dc.contributor.author | Li, Jie Liang | - |
dc.contributor.author | Zhou, Run Hong | - |
dc.contributor.author | Zhou, Yu | - |
dc.contributor.author | Wang, Yi Zhong | - |
dc.contributor.author | Zhou, Wang | - |
dc.contributor.author | Ho, Wen Zhe | - |
dc.date.accessioned | 2022-11-03T02:21:01Z | - |
dc.date.available | 2022-11-03T02:21:01Z | - |
dc.date.issued | 2017 | - |
dc.identifier.citation | Frontiers in Immunology, 2017, v. 8, n. MAR, article no. 210 | - |
dc.identifier.uri | http://hdl.handle.net/10722/321723 | - |
dc.description.abstract | Type III interferons (IFN-λs) have been demonstrated to inhibit a number of viruses, including HIV. Here, we further examined the anti-HIV effect of IFN-λs in macrophages. We found that IFN-λs synergistically enhanced anti-HIV activity of antiretrovirals [azidothymidine (AZT), efavirenz, indinavir, and enfuvirtide] in infected macrophages. Importantly, IFN-λs could suppress HIV infection of macrophages with the drug-resistant strains, including AZT-resistant virus (A012) and reverse transcriptase inhibitor-resistant virus (TC49). Mechanistically, IFN-λs were able to induce the expression of several important anti-HIV cellular factors, including myxovirus resistance 2 (Mx2), a newly identified HIV post-entry inhibitor and tetherin, a restriction factor that blocks HIV release from infected cells. These observations provide additional evidence to support the potential use of IFN-λs as therapeutics agents for the treatment of HIV infection. | - |
dc.language | eng | - |
dc.relation.ispartof | Frontiers in Immunology | - |
dc.rights | This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. | - |
dc.subject | Antiretrovirals | - |
dc.subject | Drug-resistant HIV | - |
dc.subject | IFN-λ | - |
dc.subject | Mx2 | - |
dc.subject | Tetherin | - |
dc.title | IFN-λ inhibits drug-resistant HIV infection of macrophages | - |
dc.type | Article | - |
dc.description.nature | published_or_final_version | - |
dc.identifier.doi | 10.3389/fimmu.2017.00210 | - |
dc.identifier.pmid | 28321215 | - |
dc.identifier.pmcid | PMC5337814 | - |
dc.identifier.scopus | eid_2-s2.0-85017204325 | - |
dc.identifier.volume | 8 | - |
dc.identifier.issue | MAR | - |
dc.identifier.spage | article no. 210 | - |
dc.identifier.epage | article no. 210 | - |
dc.identifier.eissn | 1664-3224 | - |
dc.identifier.isi | WOS:000395545200001 | - |