Evidence map›Paper›PMID 40622544›Full record

ReviewAdvances in experimental medicine and biology2025

Innate Immune Response to Viral Infection.

Nazar Beirag, Praveen M Varghese, Uday Kishore

Abstract readReview
PubMed Publisher
In one paragraph

Review in Advances in experimental medicine and biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Role of autophagy in antiviral innate immunity.Cellular & molecular biology letters · 2026
    Review
  5. Review
  6. Review
  7. PulmonaromFrontiers in cellular and infection microbiology · 2026
    Article
  8. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Nazar BeiragDepartment of Clinical Microbiology, Umea University, Umea, Sweden.
Praveen M VargheseDepartment of Clinical Microbiology, Umeå University, Umeå, Sweden.
Uday KishoreDepartment of Veterinary Medicine (CAVM), United Arab Emirates University, Al Ain, United Arab Emirates. uday.kishore@uaeu.ac.ae.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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.

Indexed as

Immunity, InnateVirus DiseasesVirusesAnimalsHost-Pathogen InteractionsHumansVirus Replication

Identifiers

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.