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


Journal

Journal of translational medicine
ISSN: 1479-5876
Titre abrégé: J Transl Med
Pays: England
ID NLM: 101190741

Informations de publication

Date de publication:
30 Sep 2024
Historique:
received: 22 06 2024
accepted: 23 09 2024
medline: 1 10 2024
pubmed: 1 10 2024
entrez: 1 10 2024
Statut: epublish

Résumé

To 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. Patients 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. In 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 This study demonstrates that GluR3B antibody may influence the progression of epilepsy through altering the proportion of CD4

Identifiants

pubmed: 39350251
doi: 10.1186/s12967-024-05699-2
pii: 10.1186/s12967-024-05699-2
doi:

Substances chimiques

glutamate receptor ionotropic, AMPA 3 0
Cytokines 0
Receptors, AMPA 0
Inflammation Mediators 0
Autoantibodies 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

877

Subventions

Organisme : Jiangsu Key Laboratory of New Drug Research and Clinical Pharmacy
ID : KF-XY201904
Organisme : Natural Science Foundation of Jiangsu Province
ID : BK20221221
Organisme : Fundamental Research Funds for the Central Universities
ID : 2020QN84
Organisme : Xuzhou Science and Technology Program
ID : XWKYHT20210582

Informations de copyright

© 2024. The Author(s).

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Auteurs

Qingwei Lai (Q)

Jiangsu Key Laboratory of New Drug Research and Clinical Pharmacy, Xuzhou Medical University, Xuzhou, China. lqw8696@163.com.
Department of Neurology, Affiliated Hospital of Xuzhou Medical University, 99 West Huaihai Road, Xuzhou, Jiangsu, 221002, China. lqw8696@163.com.

Nuan Wang (N)

China University of Mining and Technology, Xuzhou, China.
Department of Neurology, First People's Hospital of Xuzhou, Xuzhou, China.

Binbin Wang (B)

Department of Neurology, People's Hospital of Suining, Xuzhou, China.

Yue Chen (Y)

Department of Neurology, Affiliated Hospital of Xuzhou Medical University, 99 West Huaihai Road, Xuzhou, Jiangsu, 221002, China.

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