Epigenetic and metabolic programming of innate immunity in sepsis

Sepsis, the 10th leading cause of death, is the most expensive condition in the United States. The immune response in sepsis transitions from hyperinflammatory to a hypoinflammatory and immunosuppressive phase; individual variations regarding timing and overlap between hyper- and hypoinflammation ex...

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Main Authors: Vidula Vachharajani, Charles E McCall
Format: Article
Language:English
Published: SAGE Publishing 2019-07-01
Series:Innate Immunity
Online Access:https://doi.org/10.1177/1753425919842320
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author Vidula Vachharajani
Charles E McCall
author_facet Vidula Vachharajani
Charles E McCall
author_sort Vidula Vachharajani
collection DOAJ
description Sepsis, the 10th leading cause of death, is the most expensive condition in the United States. The immune response in sepsis transitions from hyperinflammatory to a hypoinflammatory and immunosuppressive phase; individual variations regarding timing and overlap between hyper- and hypoinflammation exist in a number of patients. While one third of the sepsis-related deaths occur during hyperinflammation, majority of the sepsis-mortality occurs during the hypoinflammatory phase. Currently, no phase-specific molecular-based therapies exist to treat sepsis. Coordinated epigenetic and metabolic perturbations orchestrate this shift from hyper- to hypoinflammation in innate immune cells during sepsis. These epigenetic and metabolic changes during sepsis progression and therapeutic opportunities they pose are described in this review.
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spelling doaj.art-5efaf494a43b4fe89c79cff9a03969732022-12-22T03:00:06ZengSAGE PublishingInnate Immunity1753-42591753-42672019-07-012510.1177/1753425919842320Epigenetic and metabolic programming of innate immunity in sepsisVidula VachharajaniCharles E McCallSepsis, the 10th leading cause of death, is the most expensive condition in the United States. The immune response in sepsis transitions from hyperinflammatory to a hypoinflammatory and immunosuppressive phase; individual variations regarding timing and overlap between hyper- and hypoinflammation exist in a number of patients. While one third of the sepsis-related deaths occur during hyperinflammation, majority of the sepsis-mortality occurs during the hypoinflammatory phase. Currently, no phase-specific molecular-based therapies exist to treat sepsis. Coordinated epigenetic and metabolic perturbations orchestrate this shift from hyper- to hypoinflammation in innate immune cells during sepsis. These epigenetic and metabolic changes during sepsis progression and therapeutic opportunities they pose are described in this review.https://doi.org/10.1177/1753425919842320
spellingShingle Vidula Vachharajani
Charles E McCall
Epigenetic and metabolic programming of innate immunity in sepsis
Innate Immunity
title Epigenetic and metabolic programming of innate immunity in sepsis
title_full Epigenetic and metabolic programming of innate immunity in sepsis
title_fullStr Epigenetic and metabolic programming of innate immunity in sepsis
title_full_unstemmed Epigenetic and metabolic programming of innate immunity in sepsis
title_short Epigenetic and metabolic programming of innate immunity in sepsis
title_sort epigenetic and metabolic programming of innate immunity in sepsis
url https://doi.org/10.1177/1753425919842320
work_keys_str_mv AT vidulavachharajani epigeneticandmetabolicprogrammingofinnateimmunityinsepsis
AT charlesemccall epigeneticandmetabolicprogrammingofinnateimmunityinsepsis