Evidence map›Paper›PMID 41126194›Full record

ArticleRespiratory research2025

Impact of clinical factors and season on inflammatory cytokines in biologic-treated and untreated asthma.

Tanawin Nopsopon, Javier Cabrera-Perez, Pui Y Lee, Kailey E Brodeur, Njira L Lugogo, Evan E Hsu, Courtney LeSon, Georg Hahn, Steven A Carr, Scott T Weiss and 1 more

Abstract read
In one paragraph

Article in Respiratory research, 2025. 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

11 authors.

Tanawin NopsoponDivision of Allergy and Clinical Immunology, Department of Medicine, Brigham & Women's Hospital, 75 Francis St, Boston, MA, USA.
Javier Cabrera-PerezDivision of Allergy and Clinical Immunology, Department of Medicine, Brigham & Women's Hospital, 75 Francis St, Boston, MA, USA.
Pui Y LeeHarvard Medical School, Boston, MA, USA.
Kailey E BrodeurDivision of Immunology, Boston Children's Hospital, Boston, MA, USA.
Njira L LugogoDivision of Pulmonary and Critical Care Medicine, University of Michigan, Michigan, USA.
Evan E HsuDivision of Immunology, Boston Children's Hospital, Boston, MA, USA.
Courtney LeSonDivision of Immunology, Boston Children's Hospital, Boston, MA, USA.
Georg HahnDivision of Pharmacoepidemiology and Pharmacoeconomics, Department of Medicine, Brigham & Women's Hospital, Boston, MA, USA.
Steven A CarrBroad Institute of MIT and Harvard, Cambridge, MA, USA.
Scott T WeissHarvard Medical School, Boston, MA, USA.
Ayobami AkenroyeDivision of Allergy and Clinical Immunology, Department of Medicine, Brigham & Women's Hospital, 75 Francis St, Boston, MA, USA. aakenroye@bwh.harvard.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundClinical features influence cytokine profiles and can inform biomarker studies.

objectivesWe assessed the impact of 13 preselected patient characteristics on the circulating levels of 15 Th-1/2/17 cytokines in moderate-to-severe asthma patients on omalizumab, anti-IL-5 (mepolizumab, benralizumab), or dupilumab (n = 76) versus controls (n = 162) not yet on biologics but meeting eligibility criteria for a T2-biologic.

methodsPlasma cytokines (Olink) were analyzed for associations with these clinical/lifestyle factors using LASSO regression and observed variance explained estimated using generalized linear models. Differential expression analysis was conducted using limma.

resultsIn controls, IL-6 had the highest variance explained by clinical/lifestyle factors (50% in non-allergic rhinitis patients, 22% in allergic rhinitis), with BMI and exacerbations contributing most to this. In T2-biologics users, eotaxin-1 had the highest explained variance (26.0%) and smoking was the most linked to Th1/17 cytokines. In omalizumab users: IFN-γ (51%) was most explained (exacerbations, smoking, age). In anti-IL-5 users, eotaxin-1 (58%; BMI, sex) and in dupilumab users, IL-4 (83%) was most explained (exacerbations, sex, BMI). The association between patient characteristics and cytokine levels differed by the season of sample collection. In non-biologic users, IL-6 was the cytokine with the most explained variance in the Winter (asthma admissions accounted for most of this variance) and IL-18 in the Spring/Summer/Fall. In T2-biologic users, TNF-α was the top cytokine in the Winter (smoking accounted for most of this variance); IL-4 (allergic rhinitis), IL-33 (IgE and eosinophil), and CXCL10 (allergic rhinitis and IgE) were the top cytokines in the Spring/Summer/Fall. In differential expression analyses, IL-1β was lower in biologics users than non-biologics users.

conclusionsIn moderate-to-severe asthma, multiple clinical features and season are associated with cytokine levels and might impact inference from proteomics studies. Smoking and BMI are the key proinflammatory factors in biologics-treated and untreated patients.

Indexed as

Anti-Asthmatic AgentsAsthmaBiological ProductsCytokinesInflammation MediatorsSeasonsAdultAgedAntibodies, Monoclonal, HumanizedBiomarkersFemaleHumansMaleMiddle AgedAnti-Asthmatic AgentsAntibodies, Monoclonal, HumanizedBiological ProductsBiomarkersCytokinesInflammation MediatorsAsthmaBiomarkersBody mass indexClinical featuresCytokinesIL-1betaMonoclonal antibodyProteomicsSmokingTh1Th17Th2

Identifiers

PMID41126194
PMCPMC12542395

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.