Published August 30, 2021 | Version v1
Publication

Peripheral CD39-expressing T regulatory cells are increased and associated with relapsing-remitting multiple sclerosis in relapsing patients

Description

CD39, an ectonucleotidase that hydrolyses pro-infammatory ATP, is a marker of highly active and suppressive T regulatory cells (Tregs). Although CD39 has a role in Treg suppression and might be important in the control of neuroinfammation in relapsing-remitting multiple sclerosis (RR-MS), to date, there are contradictory reports concerning the Tregs expression of CD39 in RR-MS patients. Thus, our objectives were to assess the activity and expression of CD39, especially in Tregs from peripheral blood mononuclear cells (PBMCs) of relapsing RR-MS patients compared with control subjects and to evaluate the association of CD39+ Tregs with disability and the odds of RR-MS. The activity and expression of CD39 and the CD39+ Treg frequency were measured in PBMCs from 55 relapsing RR-MS patients (19 untreated and 36 receiving immunomodulatory treatment) and 55 age- and sex-paired controls. Moreover, the association between CD39+ Tregs and RR-MS was assessed by multivariate logistic regression. CD39 activity and the frequency of CD39-expressing Tregs were elevated in relapsing RR-MS patients. Moreover, CD39+ Tregs were signifcantly correlated with the EDSS score and were independently associated with the odds of RR-MS. Our results highlight the relevance of CD39+ Treg subset in the clinical outcomes of RR-MS.

Abstract

Andalusian Government Ministry of Health (PI-0209-2010 PI-0485-2014, PC0019-2017)

Abstract

PAIDI Program from the Andalusian Government (CTS160)

Abstract

National Net RETICEF for Aging Studies

Abstract

Red Temática de Investigación Cooperativa en Envejecimiento y Fragilidad

Abstract

RD12/0043/0012 from the Instituto de Salud Carlos III

Abstract

Spanish Ministerio de Ciencia e Innovación

Abstract

Spanish Ministerio de Educación, Cultura y Deporte (FPU13/01210)

Additional details

Created:
March 27, 2023
Modified:
November 30, 2023