Innate Immune Response to Viral Infection
- PMID: 40622544
- DOI: 10.1007/978-3-031-85340-1_8
Innate Immune Response to Viral Infection
Abstract
The innate immune system serves as the body's primary defence against all pathogen infections, including viruses. It rapidly detects and responds to viral components, enabling an effective reaction at each stage of the viral replication cycle. This chapter explores how the innate immune system utilises pattern recognition receptors, such as Toll-like receptors and RIG-I-like receptors, to identify viral structures like capsid proteins and viral nucleic acids. The activation of these receptors triggers the release of type I interferons, particularly IFN-α and IFN-β, as well as other cytokines and chemokines. These molecules are crucial in inhibiting viral replication and inducing an antiviral state in neighbouring cells. Furthermore, the cytokines and chemokines facilitate the recruitment of key innate immune cells such as macrophages, dendritic cells, and natural killer cells, which enhance the overall immune response and directly eliminate infected cells. This chapter provides a comprehensive understanding of the complex interplay between viral pathogens and the host immune system. It also examines the antiviral role of the complement system and the transition from innate to adaptive immunity, a shift often necessitated by prolonged viral replication or sophisticated immune evasion strategies employed by viruses. By detailing these interactions and emphasising the crucial roles of interferons and immune evasion strategies, this chapter highlights the importance of early innate immune responses in controlling infections.
© 2025. The Author(s), under exclusive license to Springer Nature Switzerland AG.
Similar articles
-
RNA Viruses, Toll-Like Receptors, and Cytokines: The Perfect Storm?J Innate Immun. 2025;17(1):126-153. doi: 10.1159/000543608. Epub 2025 Jan 16. J Innate Immun. 2025. PMID: 39820070 Free PMC article. Review.
-
A MicroRNA Screen Identifies the Wnt Signaling Pathway as a Regulator of the Interferon Response during Flavivirus Infection.J Virol. 2017 Mar 29;91(8):e02388-16. doi: 10.1128/JVI.02388-16. Print 2017 Apr 15. J Virol. 2017. PMID: 28148804 Free PMC article.
-
Chasing Virus Replication and Infection: PAMP-PRR Interaction Drives Type I Interferon Production, Which in Turn Activates ISG Expression and ISGylation.Viruses. 2025 Apr 4;17(4):528. doi: 10.3390/v17040528. Viruses. 2025. PMID: 40284971 Free PMC article. Review.
-
Interactions Between the Innate and Adaptive Immune Responses.Adv Exp Med Biol. 2025;1476:297-308. doi: 10.1007/978-3-031-85340-1_12. Adv Exp Med Biol. 2025. PMID: 40622548 Review.
-
Innate immune responses to SARS-CoV-2.Prog Mol Biol Transl Sci. 2024;202:127-154. doi: 10.1016/bs.pmbts.2023.11.003. Epub 2023 Dec 15. Prog Mol Biol Transl Sci. 2024. PMID: 38237984
References
-
- Afshar, M., & Gallo, R. L. (2013). Innate immune defense system of the skin. Veterinary Dermatology, 24(1), 32-e9. - DOI
-
- Al-Ahdal, M. N., Murugaiah, V., Varghese, P. M., Abozaid, S. M., Saba, I., Al-Qahtani, A. A., et al. (2018). Entry inhibition and modulation of pro-inflammatory immune response against influenza A virus by a recombinant truncated surfactant protein D. Frontiers in Immunology, 9, 1586. - PubMed - PMC - DOI
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources
Medical