The role of complement in brain injury following intracerebral hemorrhage: A review

Exp Neurol. 2021 Jun:340:113654. doi: 10.1016/j.expneurol.2021.113654. Epub 2021 Feb 20.

Abstract

Intracerebral hemorrhage (ICH) is a significant cause of death and disability and current treatment is limited to supportive measures to reduce brain edema and secondary hematoma expansion. Current evidence suggests that the complement cascade is activated early after hemorrhage and contributes to brain edema/injury in multiple ways. The aim of this review is to summarize the most recent literature about the role of the complement cascade after ICH. Primary literature demonstrating complement mediated brain edema and neurologic injury through the membrane attack complex (MAC) as well as C3a and C5a are reviewed. Further, attenuation of brain edema and improved functional outcomes are demonstrated after inhibition of specific components of the complement cascade. Conversely, complement also plays a significant role in neurologic recovery after ICH and in other neurologic disorders. We conclude that the role of complement after ICH is complex. Understanding the role of complement after ICH is essential and may elucidate possible interventions to reduce brain edema and injury.

Keywords: Brain injury; Complement; Intervention; Intracerebral hemorrhage.

Publication types

  • Research Support, N.I.H., Extramural
  • Review

MeSH terms

  • Animals
  • Aurintricarboxylic Acid / administration & dosage
  • Brain / drug effects
  • Brain / metabolism*
  • Brain / pathology
  • Brain Injuries / drug therapy
  • Brain Injuries / metabolism*
  • Brain Injuries / pathology
  • Cerebral Hemorrhage / drug therapy
  • Cerebral Hemorrhage / metabolism*
  • Cerebral Hemorrhage / pathology
  • Complement Activation / drug effects
  • Complement Activation / physiology*
  • Complement Inactivator Proteins / administration & dosage
  • Complement System Proteins / agonists
  • Complement System Proteins / metabolism*
  • Humans

Substances

  • Complement Inactivator Proteins
  • Aurintricarboxylic Acid
  • Complement System Proteins