The Potential of STING Modulation as Broad-spectrum Host Antiviral Therapeutics for RNA Viruses

The type I interferon (IFN-I) response is a crucial antiviral defense mechanism that is primarily activated by the detection of cytoplasmic DNA via the cGAS-STING pathway or cytoplasmic viral RNA via the RLR-MAVS pathway. While STING was initially recognized for its role in DNA virus immunity, emerging evidence suggests that it also plays a key role in defense against RNA viruses, by acting as a convergence point downstream of cGAS and RLR-MAVS signaling, prior to interferon gene transcription. In accordance, STING is shown to be necessary for inducing antiviral interferons and conferring resistance to RNA virus infections. However, abnormal STING signaling is suggested as the driver behind the dysregulated or delayed IFN-I responses linked to impaired viral clearance and excessive inflammation, as observed in severe cases of RNA virus diseases such as COVID-19 and dengue. This is of utmost importance as high-priority pathogens for viral outbreaks, as indicated by the WHO, are mostly RNA viruses. Despite its significance, STING has yet to be explored as a broad-spectrum host-directed strategic target (HDST). Given the increasing need for host-targeted therapeutic approaches in pandemic preparedness, STING represents a promising candidate due to its central role in antiviral immunity and IFN-I response disruption in severe viral diseases. Therefore, this article will first consider STING as a potential broad-spectrum HDST by considering, 1) how do RNA viruses on the WHO Priority Pathogen List disrupt STING signaling for immune evasion? Following, the article will explore, 2) what are current potential strategies and challenges in leveraging STING modulation as broad-spectrum host-directed therapeutics? Exploring the relevance of STING in immunity against RNA viruses and the strategic modulations within its pathway could offer novel insights into enhancing viral clearance, reducing inflammation, and improving disease outcomes across a broad spectrum of RNA viruses. This, in turn, could strengthen global health security by improving protection, preparedness, and response to emerging and re-emerging viral threats.

Authors

Institutions

Publication Details

Journal
Open Collections
Published
2026-10-15
DOI
https://doi.org/10.14288/ujemip.v9.203802
Primary Topic
interferon and immune responses
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

The Potential of STING Modulation as Broad-spectrum Host Antiviral Therapeutics for RNA Viruses

Wan Yi Liang
Open Collections
interferon and immune responses
article

The Potential of STING Modulation as Broad-spectrum Host Antiviral Therapeutics for RNA Viruses

Wan Yi Liang
article en

Abstract

The type I interferon (IFN-I) response is a crucial antiviral defense mechanism that is primarily activated by the detection of cytoplasmic DNA via the cGAS-STING pathway or cytoplasmic viral RNA via the RLR-MAVS pathway. While STING was initially recognized for its role in DNA virus immunity, emerging evidence suggests that it also plays a key role in defense against RNA viruses, by acting as a convergence point downstream of cGAS and RLR-MAVS signaling, prior to interferon gene transcription. In accordance, STING is shown to be necessary for inducing antiviral interferons and conferring resistance to RNA virus infections. However, abnormal STING signaling is suggested as the driver behind the dysregulated or delayed IFN-I responses linked to impaired viral clearance and excessive inflammation, as observed in severe cases of RNA virus diseases such as COVID-19 and dengue. This is of utmost importance as high-priority pathogens for viral outbreaks, as indicated by the WHO, are mostly RNA viruses. Despite its significance, STING has yet to be explored as a broad-spectrum host-directed strategic target (HDST). Given the increasing need for host-targeted therapeutic approaches in pandemic preparedness, STING represents a promising candidate due to its central role in antiviral immunity and IFN-I response disruption in severe viral diseases. Therefore, this article will first consider STING as a potential broad-spectrum HDST by considering, 1) how do RNA viruses on the WHO Priority Pathogen List disrupt STING signaling for immune evasion? Following, the article will explore, 2) what are current potential strategies and challenges in leveraging STING modulation as broad-spectrum host-directed therapeutics? Exploring the relevance of STING in immunity against RNA viruses and the strategic modulations within its pathway could offer novel insights into enhancing viral clearance, reducing inflammation, and improving disease outcomes across a broad spectrum of RNA viruses. This, in turn, could strengthen global health security by improving protection, preparedness, and response to emerging and re-emerging viral threats.

Open Collections
University of British Columbia (CA)
Good health and well-being
Openalex Percentile: Top 20%
interferon and immune responses
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.