Evidence map›Paper›PMID 42582076›Full record

ArticleFrontiers in immunology2026

Sex differences in ex vivo cytokine production and their association with outcome following ischemic stroke.

Marcin Piechota, Michal Korostynski, Kazimierz Weglarczyk, Maciej Siedlar, Tomasz Dziedzic

Abstract read
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Article 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.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Marcin PiechotaLaboratory of Pharmacogenomics, Maj Institute of Pharmacology, Polish Academy of Sciences, Krakow, Poland.
Michal KorostynskiLaboratory of Pharmacogenomics, Maj Institute of Pharmacology, Polish Academy of Sciences, Krakow, Poland.
Kazimierz WeglarczykDepartment of Clinical Immunology, Institute of Pediatrics, Jagiellonian University Medical College, Krakow, Poland.
Maciej SiedlarDepartment of Clinical Immunology, Institute of Pediatrics, Jagiellonian University Medical College, Krakow, Poland.
Tomasz DziedzicDepartment of Neurology, Jagiellonian University Medical College, Krakow, Poland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Animal studies suggest that post-stroke inflammatory responses are sexually dimorphic and may influence recovery. We examined whether men and women with acute ischemic stroke differ in ex vivo cytokine synthesis and whether such differences relate to functional outcome. Methods: We included 279 patients with acute ischemic stroke (mean age: 68.5 ± 12.8; 41.2% women). Blood samples collected on day 3 after stroke were stimulated with lipopolysaccharide (LPS). Ex vivo production of TNFα, IP-10, IL-1β, IL-6, IL-8, IL-10, and IL-12p70 was measured using enzyme-linked immunoassay or cytometric methods, and expression of LPS-induced cytokine and chemokine genes was assessed by RNA sequencing. Results: Greater stroke severity, lower monocyte counts, and the use of angiotensin receptor blockers were associated with decreased production of pro-inflammatory cytokines. Compared with females, males showed higher ex vivo synthesis of TNFα (mean: 2814.2 vs 2302.7 pg/mL, P = 0.003), IL-1β (1851.9 vs 1461.3 pg/mL, P = 0.002), IL-6 (14345.3 vs 11846.5 pg/mL, P = 0.004), IL-12 (7.1 vs 4.2 pg/mL, P = 0.002), and IP-10 (557.9 vs 435.1 pg/mL, P = 0.038), with correspondingly higher gene expression levels of TNFα, IL-1β, IL-6, and IL-12. In multivariable quantile regression models adjusted for cytokine-specific covariates, male sex remained significantly associated with higher levels of TNFα, IL-1β, and IL-6. Despite this sex-related difference in inflammatory response, three-month functional outcomes were similar in men and women. Conclusion: Males exhibited greater ex vivo pro-inflammatory cytokine production after ischemic stroke, but this sexual dimorphism did not translate into differences in functional recovery.

Indexed as

CytokinesIschemic StrokeAgedFemaleHumansMaleMiddle AgedSex CharacteristicsSex FactorsCytokinesangiotensin receptor blockerscytokinesgene expressionoutcomesexstroke

Identifiers

PMID42582076
PMCPMC13457051

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