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Anagrafe della Ricerca dell'Università degli Studi di Perugia.
EnglishImmunotherapy through immune checkpoint blockers (ICBs) is quickly transforming cancer treatment by improving patients’ outcomes. However, innate and acquired resistance to ICBs remain a major challenge in clinical settings. Indoleamine 2,3-dioxygenases (IDOs) are enzymes involved in tryptophan catabolism with a central immunosuppressive function within the tumor microenvironment. IDOs are over-expressed in cancer patients and have increasingly been associated with worse outcomes and a poor prognosis. Preclinical data have shown that combining IDO and checkpoint inhibition might be a valuable strategy to improve the efficacy of immunotherapy. Currently, several IDO inhibitors have been evaluated in clinical trials, showing favorable pharmacokinetic profiles and promising efficacy. This review describes the mechanisms involved in IDO-mediated immune suppression and its role in cancer immune escape, focusing on the potential clinical application of IDO inhibitors as an immunotherapy strategy for cancer treatment.
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| Titolo: | Targeting indoleamine-2,3-dioxygenase in cancer: Scientific rationale and clinical evidence | |
| Autori: | PIRRO, Matteo (Corresponding) | |
| Data di pubblicazione: | 2019 | |
| Rivista: | ||
| Abstract: | Immunotherapy through immune checkpoint blockers (ICBs) is quickly transforming cancer treatment ...by improving patients’ outcomes. However, innate and acquired resistance to ICBs remain a major challenge in clinical settings. Indoleamine 2,3-dioxygenases (IDOs) are enzymes involved in tryptophan catabolism with a central immunosuppressive function within the tumor microenvironment. IDOs are over-expressed in cancer patients and have increasingly been associated with worse outcomes and a poor prognosis. Preclinical data have shown that combining IDO and checkpoint inhibition might be a valuable strategy to improve the efficacy of immunotherapy. Currently, several IDO inhibitors have been evaluated in clinical trials, showing favorable pharmacokinetic profiles and promising efficacy. This review describes the mechanisms involved in IDO-mediated immune suppression and its role in cancer immune escape, focusing on the potential clinical application of IDO inhibitors as an immunotherapy strategy for cancer treatment. | |
| Handle: | http://hdl.handle.net/11391/1461574 | |
| Appare nelle tipologie: | 1.1 Articolo in rivista |
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