Evidence map›Paper›PMID 42317352›Full record

ArticleFrontiers in immunology2026

Cannabinoid receptor expression profiling in lymphocyte subsets reveals clinically relevant immune patterns in SLE.

Angie M Rosero, Lady J Rios-Serna, Carlos A Cañas

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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

What it found

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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

3 authors.

Angie M RoseroCIRAT: Centro de Investigación en Reumatología, Autoinmunidad y Medicina Traslacional, Universidad Icesi, Cali, Colombia.
Lady J Rios-SernaCIRAT: Centro de Investigación en Reumatología, Autoinmunidad y Medicina Traslacional, Universidad Icesi, Cali, Colombia.
Carlos A CañasCIRAT: Centro de Investigación en Reumatología, Autoinmunidad y Medicina Traslacional, Universidad Icesi, Cali, Colombia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: This study aimed to determine the expression of cannabinoid receptors in lymphocytes from patients with systemic lupus erythematosus (SLE) compared with healthy controls, and to evaluate whether receptor expression is associated with disease activity. Methods: Using peripheral blood mononuclear cells from 35 SLE patients and 35 healthy controls, we employed multiparametric flow cytometry to characterize T-cell and B-cell subpopulations and their expression of cannabinoid receptors 1 (CB1R) and 2 (CB2R). Results: Our results reveal a significant imbalance in receptor expression: SLE patients exhibited higher CB2R and lower CB1R levels compared with controls across multiple subsets. Notably, CB1R expression strongly correlated with disease activity, while patients in remission showed expression patterns more similar to healthy individuals. Furthermore, CB2R expression in specific B-cell subsets correlated with clinical manifestations, and its distribution pattern demonstrated a significant ability to distinguish between active disease and remission in ROC analysis. Discussion: These findings indicate that SLE is characterized by altered cannabinoid receptor profiles in lymphocytes, suggesting that CB1R and CB2R modulation could serve as both a clinical biomarker and a potential therapeutic target for managing the disease.

Indexed as

Lupus Erythematosus, SystemicLymphocyte SubsetsReceptor, Cannabinoid, CB1Receptor, Cannabinoid, CB2AdultBiomarkersFemaleFlow CytometryGene Expression ProfilingHumansMaleMiddle AgedYoung AdultBiomarkersCNR2 protein, humanReceptor, Cannabinoid, CB1Receptor, Cannabinoid, CB2cannabinoid receptorCB1 receptorCB2 receptorendocannabinoid systemlymphocytessystemic lupus erythematosus

Identifiers

PMID42317352
PMCPMC13272394

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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.