Neonatal Fc receptor inhibition enables adeno-associated virus gene therapy despite pre-existing humoral immunity
Advances in adeno-associated virus-based gene therapy are transforming our ability to treat rare genetic disorders and address other unmet medical needs. However, the natural prevalence of anti-adeno-associated virus neutralizing antibodies in humans currently limits the population who can benefit f...
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Veröffentlicht in: | Human gene therapy 2023-10, Vol.34 (ja), p.1022-1032 |
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Hauptverfasser: | , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
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