Abstract

Neonatal sepsis remains a major health issue worldwide, especially for low-birth weight and premature infants, with a high risk of death and devastating sequelae. Apart from antibiotics and supportive care, there is an unmet need for adjunctive treatments to improve the outcomes of neonatal sepsis. Strong and long-standing research on adult patients has shown that vascular endothelium is a key player in the pathophysiology of sepsis and sepsis-associated organ failure, through a direct interaction with pathogens, leukocytes, platelets, and the effect of soluble circulating mediators, in part produced by endothelial cells themselves. Despite abundant evidence that the neonatal immune response to sepsis is distinct from that of adults, comparable knowledge on neonatal vascular endothelium is much more limited. Neonatal endothelial cells express lower amounts of adhesion molecules compared to adult ones, and present a reduced capacity to neutralize reactive oxygen species. Conversely, available evidence on biomarkers of endothelial damage in neonates is not as robust as in adult patients, and endothelium-targeted therapeutic opportunities for neonatal sepsis are almost unexplored. Here, we summarize current knowledge on the structure of neonatal vascular endothelium, its interactions with neonatal immune system and possible endothelium-targeted diagnostic and therapeutic tools for neonatal sepsis. Furthermore, we outline areas of basic and translational research worthy of further study, to shed light on the role of vascular endothelium in the context of neonatal sepsis.

Highlights

  • Our knowledge of the anatomy and function of the immune system in early life have greatly improved over the past few decades

  • Differences between adults and neonates exist for what concerns endothelium metabolism: for example, human umbilical vein ECs (HUVECs), as compared to human microvascular endothelial cells (ECs) (HMVEC) derived from adults, express higher levels of hydrogen peroxide and lower amounts of reactive oxygen species (ROS)-neutralizing enzymes, such as superoxide dismutase 2 (SOD2) and catalase, in response to hyperglycemia [76]: this study suggests a potential epigeneticmediated difference between neonatal and adult ECs in the capacity to neutralize ROS

  • Robust evidence concerning the role of glycocalyx degradation in shaping the pathophysiology of neonatal sepsis is still lacking; its importance can be reasonably presumed when considering that the clinical course of severe neonatal sepsis and septic shock is characterized by systemic hypotension, hypoalbuminemia, diffuse edema, disseminated intravascular coagulation and, multi-organ damage and failure [67, 87]

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Summary

Introduction

Our knowledge of the anatomy and function of the immune system in early life have greatly improved over the past few decades. Clinical and experimental studies highlight the complexity of systemic inflammatory response in neonates: notwithstanding neonatal cells show a distinct and often impaired production of cytokines and chemokines (especially for some classical proinflammatory cytokines) compared to adult cells, the impaired ability in vivo to contain locally the invading pathogen(s) leads to high bacterial loads in the blood stream and distant organs.

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