Recombinant adeno-associated virus (rAAV) vectors appear, more than ever, to be efficient viral vectors for gene transfer as illustrated by the approvals of 7 drugs across Europe and the United States. Nevertheless, preexisting immunity to AAV capsid in humans remains one of the major limits for a successful clinical translation. Whereas a preexisting humoral response to AAV capsid is well documented, the prevalence of preexisting capsid-specific T cell responses still needs to be studied and characterized.
View Article and Find Full Text PDF