| Literature DB >> 12893754 |
David-Alexandre Gross1, Marylene Leboeuf, Bernard Gjata, Olivier Danos, Jean Davoust.
Abstract
Like cellular transplantation, gene therapy is often limited by immune rejection of the newly expressed antigen. In a model of gene transfer in muscle, delivery of the influenza hemagglutinin (HA) membrane protein by adeno-associated virus (AAV) is impaired by a strong immune response that leads to a rapid rejection of the transduced fibers. We show here that injection of HA-specific CD4+CD25+ T cells from T-cell receptor (TCR)-transgenic animals, concomitant with gene transfer, down-regulates the anti-HA cytotoxic and B-lymphocyte responses and enables persistent HA expression in muscle. This demonstrates for the first time that adoptive transfer of antigen-specific CD4+CD25+ regulatory T cells can be used to induce sustained transgene engraftment in solid tissues.Entities:
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Year: 2003 PMID: 12893754 DOI: 10.1182/blood-2003-05-1454
Source DB: PubMed Journal: Blood ISSN: 0006-4971 Impact factor: 22.113