Evidence map›Paper›PMID 40120088›Full record

ReviewClinical and translational allergy2025

Eosinophils and COVID-19: Insights into immune complexity and vaccine safety.

Wided Sahli, Joana Vitte, Benoit Desnues

Erratum issuedAbstract readReview
In one paragraph

Review in Clinical and translational allergy, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. 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. COVID-19, the disease that changed the world.Medicine and pharmacy reports · 2026
    Review
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  3. Review
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  5. Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors.

Wided SahliAix Marseille University, MEPHI, Marseille, France.
Joana VitteLaboratory of Immunology, University Hospital of Reims, Reims, France.ORCID https://orcid.org/0000-0002-3344-9408
Benoit DesnuesAix Marseille University, MEPHI, Marseille, France.ORCID https://orcid.org/0000-0003-1422-4294

Funding

Agence Nationale de la Recherche 10-IAHU-03Ministère de l'Enseignement Supérieur, de la Recherche et de l'InnovationMinistère des Solidarités et de la Santé
6 · The paper itself

Abstract

backgroundCOVID-19 exhibits a variety of symptoms and may lead to multi-organ failure and death. This clinical complexity is exacerbated by significant immune dysregulation affecting nearly all cells of the innate and adaptive immune system. Granulocytes, including eosinophils, are affected by SARS-CoV-2.

objectivesEosinophil responses remain poorly understood despite early recognition of eosinopenia as a hallmark feature of COVID-19 severity.

resultsThe heterogeneous nature of eosinophil responses categorizes them as dual-function cells with contradictory effects. Eosinophil activation can suppress virus-induced inflammation by releasing type 2 cytokines like IL-13 and granular proteins with antiviral action such as eosinophil-derived neurotoxins and eosinophil cationic protein, and also by acting as antigen-presenting cells. In contrast, eosinophil accumulation in the lungs can induce tissue damage triggered by cytokines or hormones like IFN-γ and leptin. Additionally, they can affect adaptive immune functions by interacting with T cells through direct formation of membrane complexes or soluble mediator action. Individuals with allergic disorders who have elevated levels of eosinophils in tissues and blood, such as asthma, do not appear to be at an increased risk of developing severe COVID-19 following SARS-CoV-2 infection. However, the SARS-CoV-2 vaccine appears to be associated with complications and eosinophilic infiltrate-induced immunopathogenicity, which can be mitigated by corticosteroid, anti-histamines and anti-IL-5 therapy and avoided by modifying adjuvants or excipients.

conclusionThis review highlights the importance of eosinophils in COVID-19 and contributes to a better understanding of their role during natural infection and vaccination.

Indexed as

COVID‐19eosinophilsinflammationribonucleasestissue infiltrationvaccination

Identifiers

PMID40120088
PMCPMC11929522

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Registered trials

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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.