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2-Arachidonoylglycerol Reduces the Production of Interferon-Gamma in T Lymphocytes from Patients with Systemic Lupus Erythematosus.

Authors :
Navarini, Luca
Vomero, Marta
Di Donato, Stefano
Currado, Damiano
Berardicurti, Onorina
Marino, Annalisa
Bearzi, Pietro
Biaggi, Alice
Ferrito, Matteo
Ruscitti, Piero
Fava, Marina
Leuti, Alessandro
Cipriani, Paola
Maccarrone, Mauro
Giacomelli, Roberto
Source :
Biomedicines; Jul2022, Vol. 10 Issue 7, pN.PAG-N.PAG, 12p
Publication Year :
2022

Abstract

Background: the endocannabinoid 2-arachidonoylglycerol (2-AG) plays a pivotal role in immune cells regulation. The plasma levels of 2-AG are increased in patients with systemic lupus erythematosus (SLE) and correlate with disease activity. Moreover, in plasmacytoid dendritic cells from SLE patients, 2-AG is able to control the production of type 1 interferon (IFN) through CB<subscript>2</subscript> activation. The aim of this study was to evaluate the potential role of 2-AG on T lymphocytes from SLE patients. Methods: peripheral blood mononuclear cells (PBMCs) from SLE participants and age- and sex-matched healthy donors (HD) were isolated by Ficoll–Hypaque density-gradient centrifugation. The PBMCs were treated with increasing concentrations of 2-AG, and AM251 and AM630 were used to antagonize CB<subscript>1</subscript> and CB<subscript>2,</subscript> respectively. Flow cytometry was used to assess the expression of CD3, CD4, CD8, CD25, IFN-ɣ, IL-4, and IL-17A. Results: 2-AG (1 μM) decreased IFN-ɣ expression (p = 0.0005) in the Th1 lymphocytes of SLE patients. 2-AG did not modulate the cytokine expression of any other T lymphocyte population from either SLE or HD. Treatment with both 2-AG and AM630 increased the IFN-ɣ expression in Th1 lymphocytes of SLE patients (p = 0.03). Discussion: 2-AG is able to modulate type 2 IFN production from CD4+ T lymphocytes from SLE patients through CB<subscript>2</subscript> activation. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
22279059
Volume :
10
Issue :
7
Database :
Complementary Index
Journal :
Biomedicines
Publication Type :
Academic Journal
Accession number :
158212345
Full Text :
https://doi.org/10.3390/biomedicines10071675