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- W2296555766 abstract "Haem-oxygenase-1 (HO-1) is an enzyme responsible for the degradation of haem that can suppress inflammation, through the production of carbon monoxide (CO). It has been shown in several experimental models that genetic and pharmacological induction of HO-1, as well as non-toxic administration of CO, can reduce inflammatory diseases, such as endotoxic shock, type 1 diabetes and graft rejection. Recently, it was shown that the HO-1/CO system can alter the function of antigen-presenting cells (APCs) and reduce T-cell priming, which can be beneficial during immune-driven inflammatory diseases. The molecular mechanisms by which the HO-1 and CO reduce both APC- and T-cell-driven immunity are just beginning to be elucidated. In this article we discuss recent findings related to the immune regulatory capacity of HO-1 and CO at the level of recognition of pathogen-associated molecular patterns and T-cell priming by APCs. Finally, we propose a possible regulatory role for HO-1 and CO over the recently described mitochondria-dependent immunity. These concepts could contribute to the design of new therapeutic tools for inflammation-based diseases." @default.
- W2296555766 created "2016-06-24" @default.
- W2296555766 creator A5009860045 @default.
- W2296555766 creator A5020218730 @default.
- W2296555766 creator A5030575789 @default.
- W2296555766 creator A5043348844 @default.
- W2296555766 creator A5045446127 @default.
- W2296555766 creator A5049617348 @default.
- W2296555766 creator A5051672609 @default.
- W2296555766 creator A5065657680 @default.
- W2296555766 date "2016-04-01" @default.
- W2296555766 modified "2023-10-18" @default.
- W2296555766 title "Modulation of antigen processing by haem-oxygenase 1. Implications on inflammation and tolerance" @default.
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