Taenia solium excretory secretory proteins (ESPs) suppresses TLR4/AKT mediated ROS formation in human macrophages via hsa-miR-125.
Naina AroraAnand K KeshriRimanpreet KaurSuraj S RawatRajiv KumarAmit MishraAmit PrasadPublished in: PLoS neglected tropical diseases (2023)
We found that T. solium cyst ESPs treatment to human macrophages leads to activation of Th2 immune response. A complex cytokine expression by macrophages was also observed with both Th1 and Th2 cytokines in milieu. But, at the same time ESPs modulated the macrophage function by altering the host miR expression as seen with altered ROS activity, apoptosis and phagocytosis. This leads to activated yet compromised functional macrophages, which provides a niche to support parasite survival. Thus T. solium secretome induces Th2 phenomenon in macrophages which may promote parasite's survival and delay their recognition by host immune system.
Keyphrases
- immune response
- cell proliferation
- endothelial cells
- poor prognosis
- long non coding rna
- cell death
- dna damage
- signaling pathway
- inflammatory response
- long noncoding rna
- oxidative stress
- toll like receptor
- induced pluripotent stem cells
- binding protein
- pluripotent stem cells
- endoplasmic reticulum stress
- toxoplasma gondii
- dendritic cells