Review Article

The Role of Extracellular Adenosine Generation in the Development of Autoimmune Diseases

Table 1

Scheme of principal findings regarding the role of ADO and adenosinergic ectoenzymes in autoimmune diseases.

DiseaseMolecule(s) involvedPrincipal finding

Multiple sclerosisCD73, CD39Upregulation of CD73 following IFN-β treatment (14, 15)
Loss of regulatory function of CD39+ Tregs (16)

EAECD73, CD39Increase in CD73 expression during disease progression (17)
Resistance to EAE in CD73 KO mice (18, 19)
Increased enzymatic activity of CD39 and CD73 in EAE mice (20)

CIACD73Upregulation of CD73 and ADORA2A on cells from synovial fluid (21)
Increased susceptibility to CIA in CD73 KO mice (22)

Rheumatoid arthritisCD39Increased frequency of CD39+ Treg in PB of patients (23)
Increased frequency of CD39+ Treg in PB of patients responsive to MTX (24)

JIACD38, CD73Decreased expression and function of CD38 and CD73 on synovial CD56brightCD16 NK cells from patients (6)
Lower expression of CD73 in cells from synovial fluid (25)

DiabetesCD39Expression of CD39 is related to development of disease in mice (26)
Lack of ADO receptors A2A and A2B increase susceptibility to the disease (27, 28)

UveitisCD73CD73 mediates the therapeutic effect of MSC in experimental uveitis (31)
Lack of CD73 expression on γδ T cells correlated to high Th17 response (32)