Transient and intensive pharmacological immunosuppression fails to improve AAV-based liver gene transfer in non-human primates
<p><b>Abstract</b></p> <p><b>Background</b></p> <p>Adeno-associated vectors (rAAV) have been used to attain long-term liver gene expression. In humans, the cellular immune response poses a serious obstacle for transgene persistence while neutrali...
Main Authors: | , , , , , , , , , , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
BMC
2012-06-01
|
Series: | Journal of Translational Medicine |
Subjects: | |
Online Access: | http://www.translational-medicine.com/content/10/1/122 |