Table 1

 Immunoregulatory effects of administration of galectins (therapeutic and preventive) in experimental models of chronic inflammation, autoimmunity, and cancer

Experimental modelsStrategies usedClinical outcomeImmunological outcome
IFN, interferon; IL, interleukin; TNF, tumour necrosis factor.
Exogenous galectins
Experimental autoimmune myasthenia gravisElectrolectin administrationClinical recoveryNo changes in circulating autoantibodies or modifications at the muscular level
Experimental autoimmune encephalo-myelitis (multiple sclerosis)Prophylactic administration of galectin-1Prevention of clinical and histopathological manifestationsBlockade of sensitisation of pathogenic T cells
Collagen induced arthritis (rheumatoid arthritis)Galectin-1 gene therapy and protein administrationSuppression of clinical and histopathological manifestationsIncreased IL-5 and decreased IFNγ production Increased T cell susceptibility to activation induced cell death
Concanavalin A induced hepatitis (autoimmune hepatitis)Prophylactic administration of galectin-1Prevention of liver injury and T helper cell liver infiltrationSuppressed TNFα and IFNγ production Increased apoptosis of activated T cells
Inflammatory bowel disease (experimental colitis)Prophylactic and therapeutic administration of galectin-1Suppression of clinical and histopathological manifestationsReduced ability of mucosal T cells to produce IFNγ Reduced proliferation of antigen specific T cells Increased number of apoptotic T cells within mucosal tissue
Nephrotoxic nephritisGalectin-1, galectin-3, and galectin-9 administrationClinical recoveryGalectin-9 induces apoptosis of activated CD8+ cells Galectin-1 and galectin-3 block the accumulation of macrophages in the renal glomeruli
Graft v host diseaseGalectin-1 administrationIncreased host survival following allogeneic haematopoietic stem cell transplantationReduced production of IFNγ and IL-2 Reduced alloreactivity
Endogenous galectins
B16 melanomaBlockade of galectin-1 expression in the tumour microenvironment (galectin-1 knockdown clones)Increased T cell mediated tumour rejectionIncreased tumour specific IFNγ and IL-2 production Decreased number of infiltrating apoptotic T cells