| Literature DB >> 31703913 |
Scott N Ashley1, Suryanarayan Somanathan1, April R Giles1, James M Wilson2.
Abstract
An ongoing concern of in vivo gene therapy is adaptive immune responses against the protein product of a transgene, particularly for recessive diseases in which antigens are not presented to lymphocytes during central tolerance induction. Here we show that Toll-like receptor 9 (TLR9) signaling activates T cells against an epitope tagged mitochondria-targeted ornithine transcarbamylase (OTC) following the administration of a systemic adeno-associated virus (AAV) vector. Using a transgenic mouse model system, we demonstrate that TLR9 signaling extrinsic to T cells induces a robust cytotoxic T-cell response against the transgene and results in transgene expression loss. Overall, our results suggest that inflammation mediated by TLR9 signaling and the presence of high affinity transgene-specific T cells is important for the development of adaptive immune responses to transgene products following AAV gene therapy.Entities:
Keywords: AAV; Adaptive immunity; CD8(+) T cell; Gene therapy; Hepatocyte; TLR9
Mesh:
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Year: 2019 PMID: 31703913 PMCID: PMC6903695 DOI: 10.1016/j.cellimm.2019.103997
Source DB: PubMed Journal: Cell Immunol ISSN: 0008-8749 Impact factor: 4.868