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
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
15-23Subventions
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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