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Antiviral Protection by IFITM3 In Vivo

PURPOSE OF REVIEW: Interferon-induced transmembrane protein 3 (IFITM3) is a cellular restriction factor that blocks fusion between virus and host membranes. Here, we provide an introduction to IFITM3 and the biochemical regulation underlying its antiviral activity. Further, we analyze and summarize...

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Autores principales: Zani, Ashley, Yount, Jacob S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6334760/
https://www.ncbi.nlm.nih.gov/pubmed/30662816
http://dx.doi.org/10.1007/s40588-018-0103-0
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author Zani, Ashley
Yount, Jacob S.
author_facet Zani, Ashley
Yount, Jacob S.
author_sort Zani, Ashley
collection PubMed
description PURPOSE OF REVIEW: Interferon-induced transmembrane protein 3 (IFITM3) is a cellular restriction factor that blocks fusion between virus and host membranes. Here, we provide an introduction to IFITM3 and the biochemical regulation underlying its antiviral activity. Further, we analyze and summarize the published literature examining phenotypes of IFITM3 knockout mice upon infections with viral pathogens and discuss the controversial association between single nucleotide polymorphisms (SNPs) in the human IFITM3 gene and severe virus infections. RECENT FINDINGS: Recent publications show that IFITM3 knockout mice experience more severe pathologies than wild-type mice in diverse virus infections, including infections with influenza A virus, West Nile virus, Chikungunya virus, Venezuelan equine encephalitis virus, respiratory syncytial virus, and cytomegalovirus. Likewise, numerous studies of humans of Chinese ancestry have associated the IFITM3 SNP rs12252-C with severe influenza virus infections, though examinations of other populations, such as Europeans, in which this SNP is rare, have largely failed to identify an association with severe infections. A second SNP, rs34481144-A, found in the human IFITM3 promoter has also recently been reported to be a risk allele for severe influenza virus infections. SUMMARY: There is significant evidence for a protective role of IFITM3 against virus infections in both mice and humans, though additional work is required to identify the range of pathogens restricted by IFITM3 and the mechanisms by which human SNPs affect IFITM3 levels or functionality.
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spelling pubmed-63347602019-01-16 Antiviral Protection by IFITM3 In Vivo Zani, Ashley Yount, Jacob S. Curr Clin Microbiol Rep Article PURPOSE OF REVIEW: Interferon-induced transmembrane protein 3 (IFITM3) is a cellular restriction factor that blocks fusion between virus and host membranes. Here, we provide an introduction to IFITM3 and the biochemical regulation underlying its antiviral activity. Further, we analyze and summarize the published literature examining phenotypes of IFITM3 knockout mice upon infections with viral pathogens and discuss the controversial association between single nucleotide polymorphisms (SNPs) in the human IFITM3 gene and severe virus infections. RECENT FINDINGS: Recent publications show that IFITM3 knockout mice experience more severe pathologies than wild-type mice in diverse virus infections, including infections with influenza A virus, West Nile virus, Chikungunya virus, Venezuelan equine encephalitis virus, respiratory syncytial virus, and cytomegalovirus. Likewise, numerous studies of humans of Chinese ancestry have associated the IFITM3 SNP rs12252-C with severe influenza virus infections, though examinations of other populations, such as Europeans, in which this SNP is rare, have largely failed to identify an association with severe infections. A second SNP, rs34481144-A, found in the human IFITM3 promoter has also recently been reported to be a risk allele for severe influenza virus infections. SUMMARY: There is significant evidence for a protective role of IFITM3 against virus infections in both mice and humans, though additional work is required to identify the range of pathogens restricted by IFITM3 and the mechanisms by which human SNPs affect IFITM3 levels or functionality. 2018-08-03 2018-12 /pmc/articles/PMC6334760/ /pubmed/30662816 http://dx.doi.org/10.1007/s40588-018-0103-0 Text en Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Article
Zani, Ashley
Yount, Jacob S.
Antiviral Protection by IFITM3 In Vivo
title Antiviral Protection by IFITM3 In Vivo
title_full Antiviral Protection by IFITM3 In Vivo
title_fullStr Antiviral Protection by IFITM3 In Vivo
title_full_unstemmed Antiviral Protection by IFITM3 In Vivo
title_short Antiviral Protection by IFITM3 In Vivo
title_sort antiviral protection by ifitm3 in vivo
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6334760/
https://www.ncbi.nlm.nih.gov/pubmed/30662816
http://dx.doi.org/10.1007/s40588-018-0103-0
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