TY - JOUR
T1 - AAV vectors trigger DNA damage response-dependent pro-inflammatory signalling in human iPSC-derived CNS models and mouse brain
AU - Costa-Verdera, Helena
AU - Meneghini, Vasco
AU - Fitzpatrick, Zachary
AU - Abou Alezz, Monah
AU - Fabyanic, Emily
AU - Huang, Xin
AU - Dzhashiashvili, Yulia
AU - Ahiya, Avantika
AU - Mangiameli, Elisabeth
AU - Valeri, Erika
AU - Crivicich, Giovanni
AU - Piccolo, Silvia
AU - Cuccovillo, Ivan
AU - Caccia, Roberta
AU - Chan, Ying Kai
AU - Bertin, Bérangère
AU - Ronzitti, Giuseppe
AU - Engel, Esteban A.
AU - Merelli, Ivan
AU - Mingozzi, Federico
AU - Gritti, Angela
AU - Kuranda, Klaudia
AU - Kajaste-Rudnitski, Anna
N1 - Publisher Copyright:
© The Author(s) 2025.
PY - 2025/12
Y1 - 2025/12
N2 - Adeno-associated viral (AAV) vector-based gene therapy is gaining foothold as treatment for genetic neurological diseases with encouraging clinical results. Nonetheless, dose-dependent adverse events have emerged in recent clinical trials through mechanisms that remain unclear. We have modelled here the impact of AAV transduction in cell models of the human central nervous system (CNS), taking advantage of induced pluripotent stem cells. Our work uncovers vector-induced innate immune mechanisms that contribute to cell death. While empty AAV capsids were well tolerated, the AAV genome triggered p53-dependent DNA damage responses across CNS cell types followed by the induction of inflammatory responses. In addition, transgene expression led to MAVS-dependent activation of type I interferon responses. Formation of DNA damage foci in neurons and gliosis were confirmed in murine striatum upon intraparenchymal AAV injection. Transduction-induced cell death and gliosis could be prevented by inhibiting p53 or by acting downstream on STING- or IL-1R-mediated responses. Together, our work identifies innate immune mechanisms of vector sensing in the CNS that can potentially contribute to AAV-associated neurotoxicity.
AB - Adeno-associated viral (AAV) vector-based gene therapy is gaining foothold as treatment for genetic neurological diseases with encouraging clinical results. Nonetheless, dose-dependent adverse events have emerged in recent clinical trials through mechanisms that remain unclear. We have modelled here the impact of AAV transduction in cell models of the human central nervous system (CNS), taking advantage of induced pluripotent stem cells. Our work uncovers vector-induced innate immune mechanisms that contribute to cell death. While empty AAV capsids were well tolerated, the AAV genome triggered p53-dependent DNA damage responses across CNS cell types followed by the induction of inflammatory responses. In addition, transgene expression led to MAVS-dependent activation of type I interferon responses. Formation of DNA damage foci in neurons and gliosis were confirmed in murine striatum upon intraparenchymal AAV injection. Transduction-induced cell death and gliosis could be prevented by inhibiting p53 or by acting downstream on STING- or IL-1R-mediated responses. Together, our work identifies innate immune mechanisms of vector sensing in the CNS that can potentially contribute to AAV-associated neurotoxicity.
UR - https://www.scopus.com/pages/publications/105003197177
U2 - 10.1038/s41467-025-58778-3
DO - 10.1038/s41467-025-58778-3
M3 - Article
C2 - 40251179
AN - SCOPUS:105003197177
SN - 2041-1723
VL - 16
JO - Nature Communications
JF - Nature Communications
IS - 1
M1 - 3694
ER -