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Immunity in Stroke: The Next Frontier

Journal

THROMBOSIS AND HAEMOSTASIS
Volume 122, Issue 9, Pages 1454-1460

Publisher

GEORG THIEME VERLAG KG
DOI: 10.1055/s-0042-1748890

Keywords

stroke; inflammation; immunomodulatory drugs

Funding

  1. European Research Council [ERC-StGs 802305]
  2. National Natural Science Foundation of China [31600831, 81771324]
  3. German Research Foundation (DFG) [390857198]

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Inflammation plays a crucial role in ischemic stroke, both locally in the brain and systemically. New therapeutic strategies targeting inflammation are needed.
Translational stroke research has long been focusing on neuroprotective strategies to prevent secondary tissue injury and promote recovery after acute ischemic brain injury. The inflammatory response to stroke has more recently emerged as a key pathophysiological pathway contributing to stroke outcome. It is now accepted that the inflammatory response is functionally involved in all phases of the ischemic stroke pathophysiology. The immune response is therefore considered a breakthrough target for ischemic stroke treatment. On one side, stroke induces a local neuroinflammatory response, in which the inflammatory activation of glial, endothelial and brain-invading cells contributes to lesion progression after stroke. On the other side, ischemic brain injury perturbs systemic immune homeostasis and results in long-lasting changes of systemic immunity. Here, we briefly summarize current concepts in local neuroinflammation and the systemic immune responses after stroke, and highlight two promising therapeutic strategies for poststroke inflammation.

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