Therapeutic Modulation of the Complement Cascade in Stroke

Stroke is a leading cause of death and disability worldwide and an increasing number of ischemic stroke patients are undergoing pharmacological and mechanical reperfusion. Both human and experimental models of reperfused ischemic stroke have implicated the complement cascade in secondary tissue inju...

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Main Authors: Alison R. Clarke, Brandon R. Christophe, Anadjeet Khahera, Justin L. Sim, E. Sander Connolly
Format: Article
Language:English
Published: Frontiers Media S.A. 2019-07-01
Series:Frontiers in Immunology
Subjects:
Online Access:https://www.frontiersin.org/article/10.3389/fimmu.2019.01723/full
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spelling doaj-9728c9fc6b5c4d48a152b9beeba736de2020-11-25T01:09:21ZengFrontiers Media S.A.Frontiers in Immunology1664-32242019-07-011010.3389/fimmu.2019.01723471964Therapeutic Modulation of the Complement Cascade in StrokeAlison R. ClarkeBrandon R. ChristopheAnadjeet KhaheraJustin L. SimE. Sander ConnollyStroke is a leading cause of death and disability worldwide and an increasing number of ischemic stroke patients are undergoing pharmacological and mechanical reperfusion. Both human and experimental models of reperfused ischemic stroke have implicated the complement cascade in secondary tissue injury. Most data point to the lectin and alternative pathways as key to activation, and C3a and C5a binding of their receptors as critical effectors of injury. During periods of thrombolysis use to treat stroke, acute experimental complement cascade blockade has been found to rescue tissue and improves functional outcome. Blockade of the complement cascade during the period of tissue reorganization, repair, and recovery is by contrast not helpful and in fact is likely to be deleterious with emerging data suggesting downstream upregulation of the cascade might even facilitate recovery. Successful clinical translation will require the right clinical setting and pharmacologic strategies that are capable of targeting the key effectors early while not inhibiting delayed repair. Early reports in a variety of disease states suggest that such pharmacologic strategies appear to have a favorable risk profile and offer substantial hope for patients.https://www.frontiersin.org/article/10.3389/fimmu.2019.01723/fullcomplementvascular disorderscomplement activationcerebral blood flowcomplement cascadestroke therapy
collection DOAJ
language English
format Article
sources DOAJ
author Alison R. Clarke
Brandon R. Christophe
Anadjeet Khahera
Justin L. Sim
E. Sander Connolly
spellingShingle Alison R. Clarke
Brandon R. Christophe
Anadjeet Khahera
Justin L. Sim
E. Sander Connolly
Therapeutic Modulation of the Complement Cascade in Stroke
Frontiers in Immunology
complement
vascular disorders
complement activation
cerebral blood flow
complement cascade
stroke therapy
author_facet Alison R. Clarke
Brandon R. Christophe
Anadjeet Khahera
Justin L. Sim
E. Sander Connolly
author_sort Alison R. Clarke
title Therapeutic Modulation of the Complement Cascade in Stroke
title_short Therapeutic Modulation of the Complement Cascade in Stroke
title_full Therapeutic Modulation of the Complement Cascade in Stroke
title_fullStr Therapeutic Modulation of the Complement Cascade in Stroke
title_full_unstemmed Therapeutic Modulation of the Complement Cascade in Stroke
title_sort therapeutic modulation of the complement cascade in stroke
publisher Frontiers Media S.A.
series Frontiers in Immunology
issn 1664-3224
publishDate 2019-07-01
description Stroke is a leading cause of death and disability worldwide and an increasing number of ischemic stroke patients are undergoing pharmacological and mechanical reperfusion. Both human and experimental models of reperfused ischemic stroke have implicated the complement cascade in secondary tissue injury. Most data point to the lectin and alternative pathways as key to activation, and C3a and C5a binding of their receptors as critical effectors of injury. During periods of thrombolysis use to treat stroke, acute experimental complement cascade blockade has been found to rescue tissue and improves functional outcome. Blockade of the complement cascade during the period of tissue reorganization, repair, and recovery is by contrast not helpful and in fact is likely to be deleterious with emerging data suggesting downstream upregulation of the cascade might even facilitate recovery. Successful clinical translation will require the right clinical setting and pharmacologic strategies that are capable of targeting the key effectors early while not inhibiting delayed repair. Early reports in a variety of disease states suggest that such pharmacologic strategies appear to have a favorable risk profile and offer substantial hope for patients.
topic complement
vascular disorders
complement activation
cerebral blood flow
complement cascade
stroke therapy
url https://www.frontiersin.org/article/10.3389/fimmu.2019.01723/full
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AT anadjeetkhahera therapeuticmodulationofthecomplementcascadeinstroke
AT justinlsim therapeuticmodulationofthecomplementcascadeinstroke
AT esanderconnolly therapeuticmodulationofthecomplementcascadeinstroke
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