Evidence map›Paper›PMID 42666554›Full record

ReviewFrontiers in immunology2026

New perspectives in the treatment of chronic eosinophilic pneumonia in the era of targeted therapies.

Chiara Scelfo, Anna Simonazzi, Patrizia Ruggiero, Maria Rosaria Pellegrino, Nicola Facciolongo

Abstract readReview
In one paragraph

Review in Frontiers in immunology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

5 authors.

Chiara ScelfoPulmonology Unit, Arcispedale Santa Maria Nuova, Azienda USL - IRCCS di Reggio Emilia, Reggio Emilia, Italy.
Anna SimonazziPulmonology Unit, Arcispedale Santa Maria Nuova, Azienda USL - IRCCS di Reggio Emilia, Reggio Emilia, Italy.
Patrizia RuggieroPulmonology Unit, Arcispedale Santa Maria Nuova, Azienda USL - IRCCS di Reggio Emilia, Reggio Emilia, Italy.
Maria Rosaria PellegrinoPulmonology Unit, Arcispedale Santa Maria Nuova, Azienda USL - IRCCS di Reggio Emilia, Reggio Emilia, Italy.
Nicola FacciolongoPulmonology Unit, Arcispedale Santa Maria Nuova, Azienda USL - IRCCS di Reggio Emilia, Reggio Emilia, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Chronic eosinophilic pneumonia (CEP) is a rare, idiopathic inflammatory lung disease characterized by subacute symptoms such as cough, dyspnea, and fever; abnormal chest imaging findings; peripheral eosinophilia; and eosinophilic infiltration of the pulmonary interstitium and alveoli. Eosinophils interact with multiple T helper 2 (Th2) cellular pathways; however, eosinophil recruitment to the lung is primarily mediated by interleukin (IL)-5 and the eotaxin subfamily of chemokines. Standard treatment consists of systemic corticosteroids; however, relapse is frequent after tapering the corticosteroid dose, leading to long-term steroid therapy and its associated adverse effects, including diabetes mellitus, infections, glaucoma, and osteoporosis. Objective: This narrative review aims to summarize the available evidence on the effectiveness and safety of anti-IL-5 biologic therapies (mepolizumab, reslizumab, and benralizumab) in the management of CEP and as steroid-sparing strategies, with particular focus on their role in relapse prevention, which occurs in nearly 50% of cases during systemic corticosteroid tapering. Methods: A narrative review was conducted to identify the real-world advances of anti-IL-5 treatments in CEP. Most of the available literature consists of case series, case reports and observational studies, owing to the lack of controlled clinical trials and guidelines involving this disease and anti-IL-5 therapies. Results: The available evidence suggests that anti-IL-5 therapies are effective in controlling disease activity, reducing relapse rates, and enabling corticosteroid tapering or discontinuation. Conclusions: All the treatments considered were safe and well tolerated, and their use provided significant benefits in terms of symptom control, despite the limited impact on pulmonary function. Owing to their steroid-sparing effects, these agents are useful in reducing the adverse effects associated with long-term corticosteroid use. Anti-IL-5 biologics represent a promising therapeutic option for patients with relapsing or corticosteroid-dependent CEP. Despite encouraging results, larger prospective studies are needed to better define their role in the long-term management of this disease.

Indexed as

Anti-Asthmatic AgentsAntibodies, Monoclonal, HumanizedInterleukin-5Molecular Targeted TherapyPulmonary EosinophiliaAdrenal Cortex HormonesAnimalsBiological ProductsChronic DiseaseHumansSecondary PreventionTreatment OutcomeAdrenal Cortex HormonesAnti-Asthmatic AgentsAntibodies, Monoclonal, HumanizedbenralizumabBiological ProductsInterleukin-5mepolizumabreslizumabbiologic therapieschronic eosinophiiic pneumoniaeosino philsIL5steroid sparing drugs

Identifiers

PMID42666554
PMCPMC13522943

What Socratic 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 Socratic graph.