Antiviral activity of adenoviral vector expressing human interferon lambda-4 against influenza virus.
Dong-Hwi KimJae-Hyeong KimKyu-Beom LimJoong-Bok LeeSeung-Yong ParkChang-Seon SongSang-Won LeeDong-Hun LeeIn-Soo ChoiPublished in: Journal of medical virology (2024)
Interferon lambda (IFNλ), classified as a type III IFN, is a representative cytokine that plays an important role in innate immunity along with type I IFN. IFNλ can elicit antiviral states by inducing peculiar sets of IFN-stimulated genes (ISGs). In this study, an adenoviral vector expression system with a tetracycline operator system was used to express human IFNλ4 in cells and mice. The formation of recombinant adenovirus (rAd-huIFNλ4) was confirmed using immunohistochemistry assays and transmission electron microscopy. Its purity was verified by quantifying host cell DNA and host cell proteins, as well as by confirming the absence of the replication-competent adenovirus. The transduction of rAd-huIFNλ4 induced ISGs and inhibited four subtypes of the influenza virus in both mouse-derived (LA-4) and human-derived cells (A549). The antiviral state was confirmed in BALB/c mice following intranasal inoculation with 10 9 PFU of rAd-huIFNλ4, which led to the inhibition of four subtypes of the influenza virus in mouse lungs, with reduced inflammatory lesions. These results imply that human IFNλ4 could induce antiviral status by modulating ISG expression in mice.
Keyphrases
- dendritic cells
- endothelial cells
- immune response
- induced pluripotent stem cells
- induced apoptosis
- dna damage
- pluripotent stem cells
- poor prognosis
- high glucose
- dna repair
- single cell
- signaling pathway
- type diabetes
- high fat diet induced
- genome wide
- gene expression
- cell death
- metabolic syndrome
- skeletal muscle
- transcription factor
- wild type
- circulating tumor
- stress induced