Mannose-Binding Lectin: Biologic Characteristics and Role in the Susceptibility to Infections and Ischemia-Reperfusion Related Injury in Critically Ill Neonates

J Immunol Res. 2017:2017:7045630. doi: 10.1155/2017/7045630. Epub 2017 Jan 26.

Abstract

The mannose-binding lectin (MBL) is a member of the collectin family, belonging to the innate immunity system. Genetic, biologic, and clinical properties of MBL have been widely investigated throughout the last decades, although some interesting aspects of its potential clinical relevance are still poorly understood. Low circulating concentrations of MBL have been associated with increased risk of infection and poor neurologic outcome in neonates. On the other hand, an excessive and uncontrolled inflammatory response by the neonatal intestine after the exposure to luminal bacteria, leading to an increased production of MBL, may be involved in the onset of necrotizing enterocolitis. The purpose of the present review is to summarize the current knowledge about genetic and biologic characteristics of MBL and its role in the susceptibility to infections and to ischemia-reperfusion related tissue injuries to better explore its clinical relevance during the perinatal period and the possible future therapeutic applications.

Publication types

  • Review

MeSH terms

  • Critical Illness
  • Disease Susceptibility*
  • Enterocolitis, Necrotizing / immunology
  • Enterocolitis, Necrotizing / microbiology
  • Humans
  • Immunity, Innate
  • Infant, Newborn
  • Infant, Premature
  • Mannose-Binding Lectin / blood*
  • Mannose-Binding Lectin / genetics
  • Mannose-Binding Lectin / physiology*
  • Mannose-Binding Lectin / therapeutic use
  • Polymorphism, Genetic
  • Reperfusion Injury / etiology*
  • Reperfusion Injury / immunology

Substances

  • Mannose-Binding Lectin