Evidence map›Paper›PMID 39350251›Full record

ArticleJournal of translational medicine2024

The correlation of GluR3B antibody with T lymphocyte subsets and inflammatory factors and their role in the progression of epilepsy.

Qingwei Lai, Nuan Wang, Binbin Wang, Yue Chen

Abstract read
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Article in Journal of translational medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

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2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Qingwei Lai *Jiangsu Key Laboratory of New Drug Research and Clinical Pharmacy, Xuzhou Medical University, Xuzhou, China. lqw8696@163.com.ORCID 0000-0001-9805-6894
Nuan Wang *China University of Mining and Technology, Xuzhou, China.
Binbin WangDepartment of Neurology, People's Hospital of Suining, Xuzhou, China.
Yue ChenDepartment of Neurology, Affiliated Hospital of Xuzhou Medical University, 99 West Huaihai Road, Xuzhou, Jiangsu, 221002, China.

Funding

Fundamental Research Funds for the Central Universities 2020QN84Jiangsu Key Laboratory of New Drug Research and Clinical Pharmacy KF-XY201904Natural Science Foundation of Jiangsu Province BK20221221Xuzhou Science and Technology Program XWKYHT20210582
6 · The paper itself

Abstract

objectiveTo investigate changes in proportions of peripheral blood lymphocyte subsets, the correlation between the lymphocyte subsets and cytokine levels in patients with GluR3B antibody-positive epilepsy, analyze the role of GluR3B antibodies and cytokines in the progression of epilepsy. In addition, the immunotherapeutic effect in patients with GluR3B antibody-positive epilepsy will be evaluated.

methodsPatients with epilepsy hospitalized in the Department of Neurology of the affiliated Hospital of Xuzhou Medical University from December 2016 to May 2023 were recruited. GluR3B antibody levels were measured by enzyme-linked immunosorbent assay (ELISA). Lymphocyte subset proportions were determined using flow cytometry, and serum concentrations of 12 cytokines were measured using cytometric beads array. Differences in T lymphocyte subsets and inflammatory factors were analysed between GluR3B antibody positive and negative patients. Structural equation modeling (SEM) was used to analyse the role of GluR3B antibodies and inflammatory factors in drug-resistant epilepsy (DRE). Finally, the therapeutic effect of immunotherapy on epilepsy patients with GluR3B antibodies was assessed.

resultsIn this study, sixty-four cases of DRE, sixty-six cases of drug-naïve epilepsy (DNE), and forty-one cases of drug-responsive epilepsy were recruited. (1) DRE patients with positive GluR3B antibody were characterized by a significant increase in the proportion of cluster of differentiation (CD)4

conclusionsThis study demonstrates that GluR3B antibody may influence the progression of epilepsy through altering the proportion of CD4

Indexed as

CytokinesDisease ProgressionEpilepsyT-Lymphocyte SubsetsAdolescentAdultAutoantibodiesFemaleHumansInflammationInflammation MediatorsMaleMiddle AgedReceptors, AMPAYoung AdultAutoantibodiesCytokinesglutamate receptor ionotropic, AMPA 3Inflammation MediatorsReceptors, AMPAEpilepsyGluR3B antibodyImmunotherapyLymphocyte subsetsProinflammatory cytokinesStructural equation modeling

Identifiers

PMID39350251
PMCPMC11440680

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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.