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IFN-λ inhibits drug-resistant HIV infection of macrophages

  • Xu Wang
  • , He Wang
  • , Man Qing Liu
  • , Jie Liang Li
  • , Run Hong Zhou
  • , Yu Zhou
  • , Yi Zhong Wang
  • , Wang Zhou
  • , Wen Zhe Ho
  • Temple University
  • Wuhan Center for Disease Prevention and Control
  • Wuhan University

Research output: Contribution to journalArticlepeer-review

11 Scopus citations

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.

Original languageEnglish
Article number210
JournalFrontiers in Immunology
Volume8
Issue numberMAR
DOIs
StatePublished - Mar 6 2017

Keywords

  • Antiretrovirals
  • Drug-resistant HIV
  • IFN-λ
  • Mx2
  • Tetherin

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