Life sciences · Journal article
Rna Biology · September 11, 2026
No summary has been generated for this record yet. What follows is drawn from its source metadata only.
Journal article.
No findings were extractable from the material analysed.
Safety was not reported in the material analysed. Check the source before drawing any conclusion about harm.
The source did not state who this applies to in practice.
Graded across the dimensions that decide whether you should act, each from what the source actually supports. There is no single score, and where a dimension was not assessed it says so.
This record has not been graded across any dimension yet. Treat the label above as provisional and read the source.
What is missing. This record has no bottom line, key findings, reported figures, evidence dimensions. That is a gap in the analysis, not a judgement about the study.
Circular RNAs (circRNAs) are covalently closed RNA molecules with increasingly recognized roles in post-transcriptional gene regulation, immune signalling, and host-pathogen interactions. Although circRNAs have been characterized across diverse biological contexts, their roles in viral infection, particularly HIV-1, remain an underexplored area of RNA biology. Here, we review current knowledge of circRNA function in HIV-1 infection, organized into three major themes. First, we examine host-derived circRNAs, which are broadly dysregulated during infection and correlate with viral load, immune status, and antiretroviral therapy response. Second, we discuss viral-derived circRNAs, highlighting emerging evidence that HIV-1 encodes functional circRNA isoforms capable of modulating viral replication and transcription. Finally, we review synthetic circRNA-based approaches that exploit key viral RNA-protein interactions as potential antiviral tools. Collectively, these findings underscore the expanding functional roles of circRNAs in HIV-1 infection and highlight their potential as both therapeutic targets and molecular tools for future research.