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. 2024 Jul 19;17(7):963. doi: 10.3390/ph17070963

Table 3.

GAL’s immunomodulatory mechanisms.

Condition/Cell Type Mechanism of Action Key Findings Reference
Experimental Autoimmune Encephalomyelitis (EAE) Model Inhibits mononuclear cell infiltration, reduces T cell proliferation and differentiation (Th1 and Th17 cells), and impairs dendritic cell function Alleviated autoimmune encephalomyelitis [87]
LPS-stimulated RAW 264.7 Macrophage Cells Downregulates COX-2, reduces NO and proinflammatory cytokines (TNF-α, IL-1β, IL-6), and inhibits IRAK-1, JAK/STAT pathway, MAPK (p38 and ERK), and NF-κB Reduced inflammation [94]
Atopic Dermatitis (AD) Model Reduces infiltration of inflammatory cells (eosinophils, mast cells), decreases histamine levels, inhibits Th1 and Th2 cytokines, and reduces serum IgE and IgG2a Reduced inflammation [154]
Ovalbumin-(OVA-) Induced Airway Inflammation Model Reduced total leukocytes (eosinophils, neutrophils, and lymphocytes) and downregulated the production of IgE Alleviate induced airway hyperresponsiveness and inflammation [158]
Neutrophils Inhibits FcγRs and CRs activation, and reduces myeloperoxidase and horseradish peroxidase activity Decreased ROS production, reduced tissue damage [176]
Human Mast Cells (HMC)-1 Downregulates JNK, p38, and NF-κB pathways, suppresses histamine release and reduces activation of Caspase-1 Reduced inflammation [177]
Concanavalin A (ConA)-induced Hepatitis (CIH) Model Suppresses infiltration of inflammatory cells (neutrophils, macrophages, T cells), inhibits T cell activation via STAT1 pathway, and reduces proinflammatory cytokines and chemokines Reduced inflammation [178]
Bleomycin-Induced Pulmonary Fibrosis Model Reduced the number of CD4+ and CD8+ T cells and dendritic cells Alleviate pulmonary fibrosis [179]
Dendritic Cells (DCs) Promotes tolerogenic DCs (tolDCs) and stimulates regulatory T cells (Tregs) Skews DCs towards tolerogenic phenotype and suppresses inflammatory T cell responses [180]
Myocardial Ischemia-Reperfusion Injury Induces autophagic flux via PI3K/AKT/mTOR pathway, increases anti-inflammatory M2 macrophages, and decreases proinflammatory M1 macrophages Reduced inflammation [181]