Sepsis, Cytokine Storms, and Immunopathology: The Divide between Neonates and Adults
Open Access
- 28 June 2021
- journal article
- research article
- Published by Oxford University Press (OUP) in ImmunoHorizons
- Vol. 5 (6) , 512-522
Abstract
Sepsis can result from a variety of pathogens, originating from a range of sources. A vast range of presenting symptoms is included in the catch-all term of “bacteremia,” making diagnosis and prognosis particularly troublesome. One underexplored factor contributing to disparate outcomes is the age of the patient. Neonatal sepsis in very-low-birth-weight infants can result in vastly different immunological outcomes unique from sepsis in adults. It is also becoming increasingly clear, both from preclinical experimental models and clinical observations, that the age and history of previous microbial exposures can significantly influence the course of infection from sepsis and cytokine storms to immunopathology. In this study, we will explore key differences between neonatal and adult sepsis, experimental models used to study sepsis, and how responses to the surrounding microbial universe shape development of the immune system and impact, positively or negatively, the course of disease.Keywords
This publication has 150 references indexed in Scilit:
- Postoperative Sepsis in the United StatesAnnals of Surgery, 2010
- Interleukin-12 as an adjuvant for induction of protective antibody responsesCytokine, 2010
- The Harmful Role of C5a on Innate Immunity in SepsisJournal of Innate Immunity, 2010
- Pathophysiology and Treatment of Septic Shock in NeonatesClinics in Perinatology, 2010
- Murine neonatal recent thymic emigrants are phenotypically and functionally distinct from adult recent thymic emigrantsBlood, 2009
- The effects of IL-6 on CD4 T cell responsesClinical Immunology, 2009
- Antibiotic-Induced Perturbations of the Intestinal Microbiota Alter Host Susceptibility to Enteric InfectionInfection and Immunity, 2008
- Defective innate immunity predisposes murine neonates to poor sepsis outcome but is reversed by TLR agonistsBlood, 2008
- Cytomegalovirus Reactivation in Critically Ill Immunocompetent PatientsJAMA, 2008
- Hyper innate responses in neonates lead to increased morbidity and mortality after infectionProceedings of the National Academy of Sciences, 2008