MicroRNA-155 and antiviral immune responses
•miR-155 is expressed by immune cells and infected cells during viral infections.•miR-155 strongly affects both anti-virus innate and adaptive immune responses.•Irregular miR-155 expression supports virus persistence and pathologic reactions.•miR-155 may be a possible therapeutic target for treatmen...
Gespeichert in:
Veröffentlicht in: | International immunopharmacology 2021-12, Vol.101 (Pt A), p.108188-108188, Article 108188 |
---|---|
Hauptverfasser: | , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | •miR-155 is expressed by immune cells and infected cells during viral infections.•miR-155 strongly affects both anti-virus innate and adaptive immune responses.•Irregular miR-155 expression supports virus persistence and pathologic reactions.•miR-155 may be a possible therapeutic target for treatment of viral diseases.
The microRNA, miR-155 regulates both adaptive and innate immune responses. In viral infections, miR-155 can affect both innate immunity (interferon response, natural killer cell activity, and macrophage polarization) and adaptive immunity (including generation of anti-viral antibodies, CD8+ cytotoxic T lymphocytes, Th17, Th2, Th1, Tfh and Treg cells). In many viral infections, the proper and timely regulation of miR-155 expression is critical for the induction of an effective anti-virus immune response and viral clearance without any harmful immunopathologic consequences. MiR-155 may also exert pro-viral effects, mainly through the inhibition of the anti-viral interferon response. Thus, dysregulated expression of miR-155 can result in virus persistence and disruption of the normal response to viral infections. This review provides a thorough discussion of the role of miR-155 in immune responses and immunopathologic reactions during viral infections, and highlights its potential as a therapeutic target. |
---|---|
ISSN: | 1567-5769 1878-1705 |
DOI: | 10.1016/j.intimp.2021.108188 |