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IFN‐λ4 inhibits HIV infection of macrophages through signalling of IFN‐λR1/IL‐10R2 receptor complex
The recently discovered IFN‐λ4 has been found to have antiviral activity against several viruses. However, it's unknown whether IFN‐λ4 can inhibit HIV infection. Here, we show that IFN‐λ4 could suppress HIV infection of macrophages. This IFN‐λ4‐mediated HIV inhibition was compromised by the ant...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6286684/ https://www.ncbi.nlm.nih.gov/pubmed/30247785 http://dx.doi.org/10.1111/sji.12717 |
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author | Su, Qi‐Jian Wang, Xu Zhou, Run‐Hong Guo, Le Liu, Hang Li, Jie‐Liang Ho, Wen‐Zhe |
author_facet | Su, Qi‐Jian Wang, Xu Zhou, Run‐Hong Guo, Le Liu, Hang Li, Jie‐Liang Ho, Wen‐Zhe |
author_sort | Su, Qi‐Jian |
collection | PubMed |
description | The recently discovered IFN‐λ4 has been found to have antiviral activity against several viruses. However, it's unknown whether IFN‐λ4 can inhibit HIV infection. Here, we show that IFN‐λ4 could suppress HIV infection of macrophages. This IFN‐λ4‐mediated HIV inhibition was compromised by the antibodies against IFN‐λ receptor complex, IFN‐λR1/IL‐10R2. IFN‐λ4 enhanced the phosphorylation of STAT1, and induced antiviral interferon‐stimulated genes. These findings indicated that IFN‐λ4 can inhibit HIV via JAK/STAT signalling pathway. |
format | Online Article Text |
id | pubmed-6286684 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-62866842019-11-01 IFN‐λ4 inhibits HIV infection of macrophages through signalling of IFN‐λR1/IL‐10R2 receptor complex Su, Qi‐Jian Wang, Xu Zhou, Run‐Hong Guo, Le Liu, Hang Li, Jie‐Liang Ho, Wen‐Zhe Scand J Immunol Experimental Immunology The recently discovered IFN‐λ4 has been found to have antiviral activity against several viruses. However, it's unknown whether IFN‐λ4 can inhibit HIV infection. Here, we show that IFN‐λ4 could suppress HIV infection of macrophages. This IFN‐λ4‐mediated HIV inhibition was compromised by the antibodies against IFN‐λ receptor complex, IFN‐λR1/IL‐10R2. IFN‐λ4 enhanced the phosphorylation of STAT1, and induced antiviral interferon‐stimulated genes. These findings indicated that IFN‐λ4 can inhibit HIV via JAK/STAT signalling pathway. John Wiley and Sons Inc. 2018-10-10 2018-11 /pmc/articles/PMC6286684/ /pubmed/30247785 http://dx.doi.org/10.1111/sji.12717 Text en © 2018 The Foundation for the Scandinavian Journal of Immunology This article is being made freely available through PubMed Central as part of the COVID-19 public health emergency response. It can be used for unrestricted research re-use and analysis in any form or by any means with acknowledgement of the original source, for the duration of the public health emergency. |
spellingShingle | Experimental Immunology Su, Qi‐Jian Wang, Xu Zhou, Run‐Hong Guo, Le Liu, Hang Li, Jie‐Liang Ho, Wen‐Zhe IFN‐λ4 inhibits HIV infection of macrophages through signalling of IFN‐λR1/IL‐10R2 receptor complex |
title |
IFN‐λ4 inhibits HIV infection of macrophages through signalling of IFN‐λR1/IL‐10R2 receptor complex |
title_full |
IFN‐λ4 inhibits HIV infection of macrophages through signalling of IFN‐λR1/IL‐10R2 receptor complex |
title_fullStr |
IFN‐λ4 inhibits HIV infection of macrophages through signalling of IFN‐λR1/IL‐10R2 receptor complex |
title_full_unstemmed |
IFN‐λ4 inhibits HIV infection of macrophages through signalling of IFN‐λR1/IL‐10R2 receptor complex |
title_short |
IFN‐λ4 inhibits HIV infection of macrophages through signalling of IFN‐λR1/IL‐10R2 receptor complex |
title_sort | ifn‐λ4 inhibits hiv infection of macrophages through signalling of ifn‐λr1/il‐10r2 receptor complex |
topic | Experimental Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6286684/ https://www.ncbi.nlm.nih.gov/pubmed/30247785 http://dx.doi.org/10.1111/sji.12717 |
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