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Neutrophil Extracellular Traps Block Fibrinolysis in Ischemic Stroke

November 2026

M. Solo Nomenjanahary M, Desilles JP, Zemali F, Perrot A, Di Meglio L, Zalghout S, Fasille J, Neel J, Loyau S, Labreuche J, Bourrienne MC, Faille D, Delvoye F, Ollivier V, Dupont S, Rogozarski J, Brikci-Nigassa N, Medcalf RL, Ajzenberg N, Mazighi M, Ho-Tin-Noé B; compoCLOT Study Group

Abstract

Objectives: Intravenous thrombolysis (IVT) failure in acute ischemic stroke (AIS) is frequent, but its causes remain elusive. We investigated whether biologically relevant intrathrombus concentrations of tissue plasminogen activator (tPA) were achieved in failed IVT and whether neutrophil extracellular traps (NETs) contributed to this therapeutic failure.

Methods: In this monocenter cohort study, 205 thrombi from AIS patients were analyzed. A total of 83 of these thrombi were compared for tPA content and 53 for their susceptibility to ex vivo thrombolysis according to IVT status. An additional subset of 69 AIS thrombi was used to decipher if and how NETs interfere with intrathrombus fibrinolysis.

Results: Thrombi from IVT patients contained twice as much tPA than those from no-IVT patients (p < 0.0001). Plasminogen and tPA in AIS thrombi were associated with fibrin, leukocytes, and NETs. Although ex vivo addition of plasminogen did not cause lysis of either no-IVT or IVT thrombi, combining plasminogen with deoxyribonuclease 1 (DNase 1) helped translate the increased tPA content of IVT thrombi into increased thrombolysis. We further show that DNase 1 enables tPA- and plasmin-mediated thrombolysis by eliminating fibrinolysis inhibitors from AIS thrombi.

 

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