# Decoding miRNA-Mediated Immunoregulation in SARS-CoV-2, HBV, HIV, and HSV Infections

**Authors:** Suleyman Arziman, Sevim Aydemir, Vildan Bozok

PMC · DOI: 10.1038/s41435-026-00376-4 · 2026-01-20

## TL;DR

This paper reviews how microRNAs regulate immune responses in four major viral infections, highlighting their roles in disease progression and potential as therapeutic targets.

## Contribution

The paper provides a comprehensive synthesis of recent findings on miRNA-mediated immunoregulation in SARS-CoV-2, HBV, HIV, and HSV infections.

## Key findings

- miRNAs like miR-21, miR-146a, miR-150, and miR-155 modulate key immune signaling pathways during viral infections.
- Virus-encoded miRNAs and ceRNA interactions add regulatory layers specific to each virus.
- miRNAs influence macrophage polarization, T/NK cell activity, and cytokine production, impacting antiviral immunity.

## Abstract

Eukaryotic cells regulate gene expression through multiple checkpoints, including post-transcriptional mechanisms mediated by microRNAs (miRNAs). These small non-coding RNAs inhibit translation by binding to target mRNAs, often within a complex regulatory network involving other RNA species such as circular RNAs and long non-coding RNAs. miRNAs are now recognised as central players in the pathogenesis, immune modulation, and progression of infectious diseases. In this review, we thoroughly examine studies published over the past five years, focusing on miRNAs involved in immune regulation during four major viral infections: severe acute respiratory syndrome coronavirus 2, hepatitis B virus, human immunodeficiency virus, and herpes simplex virus. Our analysis centres on the core signalling pathways most frequently targeted by miRNAs: NF-κB, MAPK, JAK-STAT, TGF-β/Smad, and pattern-recognition receptor-associated cascades. Among the miRNAs most prominently implicated are miR-21, miR-146a, miR-150, and miR-155. These miRNAs modulate key signalling pathways, thereby influencing macrophage polarisation, T- and natural killer cell activity, antigen presentation, and inflammatory cytokine production. In addition, virus-encoded miRNAs and ceRNA or extracellular vesicle-mediated interactions are discussed where mechanistically validated, illustrating virus-specific regulatory layers. Collectively, this integrative synthesis underscores the pivotal roles of miRNAs in orchestrating antiviral immunity and highlights their potential as biomarkers and therapeutic targets in viral infections. A better understanding of miRNA-mediated immunoregulation may pave the way for precision interventions aimed at improving immune control and patient outcomes.

## Linked entities

- **Diseases:** severe acute respiratory syndrome coronavirus 2 (MONDO:0100096)

## Full-text entities

- **Genes:** MIR21 (microRNA 21) [NCBI Gene 406991] {aka MIRN21, hsa-mir-21, miR-21, miRNA21}, TGFB1 (transforming growth factor beta 1) [NCBI Gene 7040] {aka CAEND1, CED, DPD1, IBDIMDE, LAP, TGF-beta1}, MIR150 (microRNA 150) [NCBI Gene 406942] {aka MIRN150, miRNA150, mir-150}, MIR146A (microRNA 146a) [NCBI Gene 406938] {aka MIRN146, MIRN146A, miR-146a, miRNA146A}, MIR155 (microRNA 155) [NCBI Gene 406947] {aka MIRN155, miRNA155, mir-155}, NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790] {aka CVID12, EBP-1, KBF1, NF-kB, NF-kB1, NF-kappa-B1}
- **Diseases:** infectious diseases (MESH:D003141), HBV, HIV, and HSV Infections (MESH:C536395), inflammatory (MESH:D007249), viral infections (MESH:D014777), SARS-CoV-2 (MESH:D000086382)
- **Species:** Human immunodeficiency virus (species) [taxon 12721], Homo sapiens (human, species) [taxon 9606], Hepatitis B virus (no rank) [taxon 10407], Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049]

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12923359/full.md

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Source: https://tomesphere.com/paper/PMC12923359