Mingozzi Federico, Maus Marcela V, Hui Daniel J, Sabatino Denise E, Murphy Samuel L, Rasko John E J, Ragni Margaret V, Manno Catherine S, Sommer Jurg, Jiang Haiyan, Pierce Glenn F, Ertl Hildegund C J, High Katherine A
The Children's Hospital of Philadelphia, 3615 Civic Center Boulevard, Philadelphia, Pennsylvania 19104, USA.
Nat Med. 2007 Apr;13(4):419-22. doi: 10.1038/nm1549. Epub 2007 Mar 18.
Hepatic adeno-associated virus (AAV)-serotype 2 mediated gene transfer results in transgene product expression that is sustained in experimental animals but not in human subjects. We hypothesize that this is caused by rejection of transduced hepatocytes by AAV capsid-specific memory CD8(+) T cells reactivated by AAV vectors. Here we show that healthy subjects carry AAV capsid-specific CD8(+) T cells and that AAV-mediated gene transfer results in their expansion. No such expansion occurs in mice after AAV-mediated gene transfer. In addition, we show that AAV-2 induced human T cells proliferate upon exposure to alternate AAV serotypes, indicating that other serotypes are unlikely to evade capsid-specific immune responses.
肝相关腺病毒(AAV)2型介导的基因转移导致转基因产物表达,这种表达在实验动物中能够持续,但在人类受试者中却不能。我们推测,这是由AAV载体重新激活的AAV衣壳特异性记忆CD8(+) T细胞对转导的肝细胞的排斥所导致的。在此我们表明,健康受试者携带AAV衣壳特异性CD8(+) T细胞,并且AAV介导的基因转移会导致这些细胞扩增。在AAV介导的基因转移后,小鼠中不会发生这种扩增。此外,我们表明,AAV-2诱导的人类T细胞在暴露于其他AAV血清型时会增殖,这表明其他血清型不太可能逃避衣壳特异性免疫反应。