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Fatal thrombotic microangiopathy case following adeno-associated viral SMN gene therapy.

Julia GuillouAlice de PellegarsFlorence PorcheretVéronique Frémeaux- BacchiEmma Allain-LaunayCamille DebordManon DenisYann PéréonChristine BarnériasIsabelle DesguerreGwenaëlle RousseySandra Mercier
Published in: Blood advances (2022)
Adeno-associated virus (AAV) gene therapies are highly promising, such as the onasemnogene abeparvovec (Zolgensma) in spinal muscle atrophy (SMA). We report the first case of fatal systemic thrombotic microangiopathy (TMA) following onasemnogene abeparvovec in a 6-month-old child with SMA type 1, carrying a potential genetic predisposition in the complement factor I gene. Other cases of TMA have recently been reported after onasemnogene abeparvovec and after AAV9 minidystrophin therapy in Duchenne muscular dystrophy. The risk-benefit ratio of this therapy must therefore be assessed. Early recognition of TMA and targeted immunotherapy are fundamental to ensure the safety of patients treated with AAV gene therapies.
Keyphrases
  • gene therapy
  • duchenne muscular dystrophy
  • genome wide
  • copy number
  • genome wide identification
  • mental health
  • sars cov
  • dna methylation
  • stem cells
  • transcription factor
  • climate change