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- W2901827774 abstract "We took an experimental database mining analysis to determine the expression of 28 co-signaling receptors in 32 human tissues in physiological/pathological conditions. We made the following significant findings: 1) co-signaling receptors are differentially expressed in tissues; 2) heart, trachea, kidney, mammary gland and muscle express co-signaling receptors that mediate CD4+T cell functions such as priming, differentiation, effector, and memory; 3) urinary tumor, germ cell tumor, leukemia and chondrosarcoma express high levels of co-signaling receptors for T cell activation; 4) expression of inflammasome components are correlated with the expression of co-signaling receptors; 5) CD40, SLAM, CD80 are differentially expressed in leukocytes from patients with trauma, bacterial infections, polarized macrophages and in activated endothelial cells; 6) forward and reverse signaling of 50% co-inhibition receptors are upregulated in endothelial cells during inflammation; and 7) STAT1 deficiency in T cells upregulates MHC class II and co-stimulation receptors. Our results have provided novel insights into co-signaling receptors as physiological regulators and potentiate identification of new therapeutic targets for the treatment of sterile inflammatory disorders." @default.
- W2901827774 created "2018-11-29" @default.
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- W2901827774 date "2019-01-01" @default.
- W2901827774 modified "2023-09-22" @default.
- W2901827774 title "Co-signaling receptors regulate T-cell plasticity and immune tolerance" @default.
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- W2901827774 doi "https://doi.org/10.2741/4710" @default.
- W2901827774 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/6309335" @default.
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- W2901827774 hasPublicationYear "2019" @default.
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