Regulatory T cell profiles in patients with

Brain inflammation CCR6 receptors Regulatory T cells Suppressor T cells

Journal

Encephalitis (Seoul, Korea)
ISSN: 2734-1461
Titre abrégé: Encephalitis
Pays: Korea (South)
ID NLM: 9918592381006676

Informations de publication

Date de publication:
Jan 2023
Historique:
received: 02 08 2022
revised: 24 09 2022
accepted: 30 09 2022
medline: 20 7 2023
pubmed: 20 7 2023
entrez: 20 7 2023
Statut: ppublish

Résumé

Purpose Regulatory T cells (Tregs) have been implicated in the pathogenesis of several autoimmune disorders and used in adoptive cell transfer therapies. Neither have been explored in patients with autoimmune encephalitis where treated patient outcomes remain suboptimal with frequent relapses. Here, to identify new treatment strategies for autoimmune encephalitis, we sought to evaluate the proportion of circulating Tregs and Treg subpopulations in peripheral blood of patients with We compared the phenotype of peripheral blood Tregs in four adult NMDAR-Ab-E patients and four age- and sex-matched healthy controls using an 11-color flow cytometry assay panel for characterization of Tregs (CD4+ CD25+ FoxP3+) cells into naïve (chemokine receptor [CCR] 7+ CD45RA+), central memory (CCR7+ CD45RA-), and effector memory (CCR7- CD45RA-) cells. We also examined and compared the expression of the CCR6 by circulating Tregs and the respective Treg subpopulations between the study groups. The proportion of circulating Tregs was similar between patients with NMDAR-Ab-E and healthy controls but the proportion of naïve Tregs was lower in NMDAR-Ab-E patients (p = 0.0026). Additionally, the frequency of circulating effector memory Tregs was higher, and the proportion of circulating effector memory Tregs expressing CCR6 was lower, in NMDAR-Ab-E patients compared with healthy controls (p = 0.0026). Altered Treg homeostasis may be a feature of patients with NMDAR-Ab-E. Future studies with larger samples are warranted to validate these findings.

Identifiants

pubmed: 37469716
doi: 10.47936/encephalitis.2022.00052
pii: encephalitis-2022-00052
pmc: PMC10295821
doi:

Types de publication

Journal Article

Langues

eng

Pagination

15-23

Subventions

Organisme : Medical Research Council
ID : MR/V007173/1
Pays : United Kingdom

Informations de copyright

Copyright © 2023 Korean Encephalitis and Neuroinflammation Society.

Déclaration de conflit d'intérêts

Conflicts of Interest Irani SR is an inventor of ‘Diagnostic Strategy to improve specificity of CASPR2 antibody detection (PCT/G82019/051257)' and receives royalties on a licensed patent application for LGI1/CASPR2 testing as co-applicant (PCT/GB2009/051441) entitled “Neurological Autoimmune Disorders.” Irani SR has received honoraria and/or research support from UCB, Immunovant, MedImmun, Roche, Janssen, Cerebral therapeutics, CSL Behring, and ONO Pharma. Iro MA is funded by Health Education England (HEE) / NIHR for this research project. No other potential conflict of interest relevant to this article was reported.

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Auteurs

Mildred A Iro (MA)

Faculty of Medicine and Institute of Life Sciences, University of Southampton, United Kingdom.
Department of Paediatric Infectious Diseases, Southampton Children's Hospital, University Hospital Southampton NHS Foundation Trust, Southampton, United Kingdom.

Christine S Rollier (CS)

Oxford Vaccine Group, Department of Paediatrics, University of Oxford, and the NIHR Oxford Biomedical Research Centre, Oxford, United Kingdom.
School of Biosciences, Faculty of Health and Medical Sciences, University of Surrey, Guildford, United Kingdom.

Sarosh R Irani (SR)

Oxford Autoimmune Neurology Group, Nuffield Department of Clinical Neurosciences, University of Oxford, Oxford, United Kingdom.
Department of Neurology, John Radcliffe Hospital, Oxford University Hospitals NHS Foundation, Trust, Oxford, United Kingdom.

Manish Sadarangani (M)

Vaccine Evaluation Center, BC Children's Hospital Research Institute, Vancouver, BC, Canada.
Department of Pediatrics, University of British Columbia, Vancouver, BC, Canada.

Adam Al-Diwani (A)

Oxford Autoimmune Neurology Group, Nuffield Department of Clinical Neurosciences, University of Oxford, Oxford, United Kingdom.
University Department of Psychiatry, University of Oxford, Oxford, United Kingdom.

Andrew J Pollard (AJ)

Oxford Vaccine Group, Department of Paediatrics, University of Oxford, and the NIHR Oxford Biomedical Research Centre, Oxford, United Kingdom.

Elizabeth A Clutterbuck (EA)

Oxford Vaccine Group, Department of Paediatrics, University of Oxford, and the NIHR Oxford Biomedical Research Centre, Oxford, United Kingdom.

Classifications MeSH