Related Experiment Video

Updated: Sep 21, 2026

Rescue of Recombinant Newcastle Disease Virus from cDNA
10:55

Rescue of Recombinant Newcastle Disease Virus from cDNA

Published on: October 11, 2013

Characteristics of antiviral and anticellular activities of human recombinant interferon-gamma

K Gomi, M Morimoto, N Nakamizo

    Japanese Journal of Cancer Research : Gann
    |March 1, 1985
    PubMed

    The antiviral and anticellular activities of recombinant human interferon-gamma (Re-IFN-gamma) were compared with those of natural human interferon-gamma (IFN-gamma), natural human interferon-alpha (IFN-alpha), and recombinant human interferon-beta (ReIFN-beta). ReIFN-gamma and IFN-gamma induced the antiviral state in FL cells against Sindbis virus more rapidly than IFN-alpha or ReIFN-beta. The antiviral state induced by a short exposure time to IFN-gamma declined rapidly after the removal of IFN-gamma and the incubation of FL cells in fresh medium, whereas that induced by ReIFN-gamma was persistent. However, other characteristics of the antiviral activity of ReIFN-gamma were shown to be very similar to those of IFN-gamma (e.g., stability at 56 degrees or pH 2.0, and neutralization by anti-IFN serum). The anticellular spectrum of ReIFN-gamma or IFN-gamma against 26 human cell lines differed in some respects from that of IFN-alpha or ReIFN-beta, since ReIFN-gamma and IFN-gamma were more effective at inhibiting the growth of human carcinoma or sarcoma cell lines. The IC50 (IFN concentration required for 50% growth inhibition) values of ReIFN-gamma were several times smaller than those of IFN-gamma in all cell lines sensitive to both IFNs. ReIFN-gamma and IFN-gamma, but not IFN-alpha or ReIFN-beta, were cytotoxic against HeLa S3 cells. These cytotoxicities of both IFNs were inactivated by treatment at 56 degrees or pH 2.0 and by anti-ReIFN-gamma serum. These results indicate that the characteristics of antiviral and anticellular activities of ReIFN-gamma are somewhat different from those of other IFNs including IFN-gamma.

    More Related Videos

    Dissecting Innate Immune Signaling in Viral Evasion of Cytokine Production08:32

    Dissecting Innate Immune Signaling in Viral Evasion of Cytokine Production

    Published on: March 2, 2014

    High-throughput Quantitative Real-time RT-PCR Assay for Determining Expression Profiles of Types I and III Interferon Subtypes10:00

    High-throughput Quantitative Real-time RT-PCR Assay for Determining Expression Profiles of Types I and III Interferon Subtypes

    Published on: March 24, 2015

    Related Concept Videos

    Antimicrobial Proteins01:23

    Antimicrobial Proteins

    Antimicrobial proteins are important components of the immune system. They aid the body in combating pathogens by either killing them directly or hindering their replication processes. Four main types of antimicrobial substances are interferons, the complement system, iron-binding proteins, and antimicrobial proteins.
    Interferons
    Interferons (IFNs) are proteins produced by lymphocytes, macrophages, and fibroblasts infected with viruses. While IFNs cannot prevent viruses from entering and...
    Immune Response Against Viral Pathogens01:29

    Immune Response Against Viral Pathogens

    The immune system's response to viral infections is a complex and coordinated process involving natural killer (NK) cells, T cell-mediated responses, and antibody-mediated responses.
    NK Cells
    NK cells are a crucial part of our innate immune system, acting as the first line of defense against viral infections. These cells can recognize and kill infected cells without prior exposure to the virus, effectively slowing down the spread of infection. Additionally, NK cells produce proinflammatory...
    Inhibitors of Viral Protein Synthesis01:30

    Inhibitors of Viral Protein Synthesis

    Protein synthesis is indispensable for viral replication, as viruses lack the cellular machinery required for this process and must hijack the host's translational apparatus. In response, host cells deploy a critical innate immune defense involving interferons, specialized cytokines that play a central role in inhibiting viral propagation.Upon viral detection, infected cells release interferons that bind to receptors on adjacent uninfected cells, activating the JAK-STAT signaling pathway and...
    Inhibitors Of Virion Release01:25

    Inhibitors Of Virion Release

    Viral replication and dissemination rely on efficient mechanisms for host cell entry, genome replication, assembly, and release. Influenza viruses, such as types A and B, are negative-sense single-stranded RNA viruses with a segmented genome, that depend on two critical surface glycoproteins to carry out these processes: hemagglutinin (HA) and neuraminidase (NA). HA initiates infection by binding to sialic acid residues on the surface of host epithelial cells, facilitating receptor-mediated...
    Antiviral Nucleoside Inhibitors01:22

    Antiviral Nucleoside Inhibitors

    Antiviral Nucleoside InhibitorsAntiviral nucleoside inhibitors are structural analogs of natural nucleosides that interfere with viral DNA or RNA synthesis. These compounds selectively target viral polymerases due to their resemblance to host nucleosides, thereby disrupting viral genome replication.Mechanism of Acyclovir ActionAcyclovir is a guanosine analog with a three-carbon acyclic side chain. It selectively targets herpes simplex virus type 1 (HSV-1), herpes simplex virus type 2 (HSV-2),...
    Inhibitors of Virion Maturation and Assembly01:19

    Inhibitors of Virion Maturation and Assembly

    As part of their replication cycle, certain viruses synthesize long precursor proteins called polyproteins within infected host cells. In human immunodeficiency virus (HIV), two major polyproteins are produced: Gag and Gag-Pol. The Gag polyprotein supplies the structural components of the virus, while Gag-Pol includes essential viral enzymes such as reverse transcriptase, integrase, and protease. After synthesis, these polyproteins move to the host cell membrane, where they assemble into an...