免疫系统
转基因
生物
遗传增强
免疫学
埃利斯波特
T细胞
基因
遗传学
作者
Julie Vendomèle,Gaëlle Anne Chauveau,Deniz Dalkara,Anne Galy,Sylvain Fisson
出处
期刊:Human Gene Therapy
[Mary Ann Liebert, Inc.]
日期:2024-06-15
卷期号:35 (13-14): 464-476
被引量:2
摘要
After more than two decades of basic research and preclinical studies, adeno-associated virus (AAV)-mediated gene transfer has been tested successfully in clinical trials to treat inherited retinal diseases. Despite the eye's immune-privileged status, some patients display inflammatory events requiring the use of corticoids as an adjunct treatment which led us to question the immune consequences of a subretinal AAV administration. We first characterized anti-transgene immune responses induced in the periphery by injecting increasing doses of AAV8 encoding reporter proteins fused with the HY male antigen into the subretinal space of female C57BL/6 and rd10 mice. Transgene expression was monitored over time with bioluminescence imaging, and T cell immune responses in the spleen were analyzed by IFNγ ELISpot and cytokine multiplex assays. Our data show that AAV8 injections cause pro-inflammatory T cell immune response against the transgene product correlated with the transgene expression level at 2.10
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