ArticleCell reports2026
SFPQ prevents MDA5-mediated activation of innate immunity and preserves cell viability.
Article in Cell reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
1 citing paper in PubMed.
- VRK3 promotes KSHV infection by suppressing the antiviral type I interferon response.PLoS pathogens · 2026Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
6 authors.
Funding
Abstract
The melanoma differentiation-associated gene 5 (MDA5) sensor recognizes double-stranded RNA (dsRNA) produced during viral infections, leading to type I interferon (IFN) production. Host proteins can shield endogenous dsRNA from MDA5 through RNA modifications, such as A-to-I editing of dsRNA by adenosine deaminase acting on RNA 1 (ADAR1). The splicing factor proline- and glutamine-rich (SFPQ) is an RNA-binding protein that regulates RNA biogenesis. However, its role in innate immunity has not been previously explored. We report that SFPQ can promote viral replication of Kaposi's sarcoma-associated herpesvirus (KSHV) and demonstrate that SFPQ can prevent IFN production not only in the context of viral replication but also in uninfected cells. Furthermore, SFPQ associates with ADAR1 and modulates A-to-I editing of cellular RNA transcripts. Moreover, SFPQ depletion in uninfected cells induced IFN response genes, including MDA5 and ZBP1, and impaired cell growth. In summary, SFPQ binds ADAR1 and modulates its editing function, thereby preventing cellular RNAs from activating MDA5-mediated innate immune responses.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.