Related Experiment Video
Updated: Jun 20, 2026

An Optimized Hemagglutination Inhibition (HI) Assay to Quantify Influenza-specific Antibody Titers
Published on: December 1, 2017
Potential targets and their relevant inhibitors in anti-influenza fields
Jianzhi Gong1, Hao Fang, Minyong Li
1Department of Medicinal Chemistry, School of Pharmaceutical Sciences, Shandong University, Jinan, Shandong, China. drgongjianzhi@yahoo.com.cn
Abstract:
Influenza is a disease for deeply affecting millions of people every year. Recently, there has been considerable concern regarding the highly pathogenic H5N1 avian influenza virus, and its human pandemic potential. With developments in viral biology, there are more novel antiviral strategies targeting these viruses. In this review, we will discuss several proven and potential anti-influenza targets, including viral factors (such as hemagglutinin (HA), M2 ion channel protein, RNA-dependent RNA polymerase (RdRp), nucleoprotein (NP), non-structural protein (NS) and neuraminidase (NA)) and host factors (such as v-ATPase, protease, inosine monophosphate dehydrogenase (IMPDH) and intracellular signalling cascades), and their relevant inhibitors.
Insights
This review explores antiviral strategies against influenza, focusing on novel targets within viral factors like hemagglutinin (HA) and host factors such as v-ATPase. It discusses inhibitors for these key targets to combat influenza infections.
Area of Science:
- Virology and Molecular Biology
- Infectious Diseases
- Drug Discovery
Background:
- Influenza affects millions annually, with significant concern over highly pathogenic H5N1 avian influenza and its pandemic potential.
- Advancements in viral biology have spurred the development of novel antiviral strategies.
- Understanding viral and host factors is crucial for effective influenza treatment.
Purpose of the Study:
- To review established and potential anti-influenza therapeutic targets.
- To discuss inhibitors targeting both viral and host factors involved in influenza replication.
- To provide an overview of current and emerging antiviral strategies against influenza viruses.
Main Methods:
- Literature review of scientific publications on influenza virology and antiviral drug development.
- Analysis of viral factors including hemagglutinin (HA), M2 ion channel protein, RNA-dependent RNA polymerase (RdRp), nucleoprotein (NP), non-structural protein (NS), and neuraminidase (NA).
- Examination of host factors such as v-ATPase, protease, inosine monophosphate dehydrogenase (IMPDH), and intracellular signaling cascades.
Main Results:
- Identified multiple viral proteins (HA, M2, RdRp, NP, NS, NA) as key targets for antiviral intervention.
- Highlighted host cellular machinery (v-ATPase, proteases, IMPDH, signaling pathways) as potential targets to disrupt viral replication.
- Summarized various inhibitors developed against these viral and host targets.
Conclusions:
- A diverse range of viral and host targets offer promising avenues for novel anti-influenza therapies.
- Targeting host factors presents a strategy to overcome viral resistance.
- Continued research into these targets and their inhibitors is essential for pandemic preparedness.
More Related Videos
04:47A Method to Assess Fc-mediated Effector Functions Induced by Influenza Hemagglutinin Specific Antibodies
Published on: February 23, 2018
09:31Fluorescence-based Neuraminidase Inhibition Assay to Assess the Susceptibility of Influenza Viruses to The Neuraminidase Inhibitor Class of Antivirals
Published on: April 15, 2017
Related Concept Videos
Inhibitors Of Virion Release
Inhibitors of Viral Protein Synthesis
Influenza
Targets for Drug Action: Overview
Receptors are either membrane-spanning or intracellular proteins, which upon binding a ligand, get activated and transmit the signal downstream to elicit a response. Drugs bind receptors, either mimicking the action of endogenous ligands or blocking the receptor activity to bring about a modified response. Nearly 35% of approved drugs target the G...
Inhibitors of Virion Maturation and Assembly