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Updated: Jan 30, 2026

Assays for the Identification of Novel Antivirals against Bluetongue Virus
Published on: October 11, 2013
Antiviral Protection by IFITM3 In Vivo
1Department of Microbial Infection and Immunity, Infectious, Diseases Institute, The Ohio State University, 460 W 12th Ave, Biomedical Research Tower 790, Columbus, OH 43210, USA.
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.
Insights
Interferon-induced transmembrane protein 3 (IFITM3) protects against diverse viral infections. Studies show IFITM3 knockout mice exhibit increased disease severity, and specific human IFITM3 gene variants are linked to severe influenza outcomes.
Area of Science:
- Virology
- Immunology
- Genetics
Background:
- Interferon-induced transmembrane protein 3 (IFITM3) acts as a cellular restriction factor, inhibiting virus-host membrane fusion.
- Understanding IFITM3's antiviral mechanisms and genetic regulation is crucial for combating viral diseases.
Purpose of the Study:
- To introduce IFITM3 and its biochemical regulation.
- To analyze IFITM3 knockout mouse phenotypes during viral infections.
- To discuss the association between IFITM3 genetic variations and severe human virus infections.
Main Methods:
- Literature review of IFITM3 function and regulation.
- Analysis of published data on IFITM3 knockout mouse models.
- Examination of genetic association studies on human IFITM3 single nucleotide polymorphisms (SNPs).
Main Results:
- IFITM3 knockout mice display heightened susceptibility and pathology across various viral infections (e.g., influenza, West Nile virus).
- The IFITM3 SNP rs12252-C is associated with severe influenza in human populations of Chinese ancestry but not typically in Europeans.
- A second SNP, rs34481144-A, in the IFITM3 promoter region is also identified as a risk factor for severe influenza.
Conclusions:
- IFITM3 plays a significant protective role against viral infections in both mice and humans.
- Further research is needed to delineate the full spectrum of viruses restricted by IFITM3.
- Investigating the precise mechanisms by which human IFITM3 SNPs influence protein levels or function is essential.
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