Literature DB >> 12893754

CD4+CD25+ regulatory T cells inhibit immune-mediated transgene rejection.

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:  

Mesh:

Substances:

Year:  2003        PMID: 12893754     DOI: 10.1182/blood-2003-05-1454

Source DB:  PubMed          Journal:  Blood        ISSN: 0006-4971            Impact factor:   22.113


  18 in total

1.  Induction and role of regulatory CD4+CD25+ T cells in tolerance to the transgene product following hepatic in vivo gene transfer.

Authors:  Ou Cao; Eric Dobrzynski; Lixin Wang; Sushrusha Nayak; Bethany Mingle; Cox Terhorst; Roland W Herzog
Journal:  Blood       Date:  2007-04-16       Impact factor: 22.113

2.  Recombinant adeno-associated virus vectors induce functionally impaired transgene product-specific CD8+ T cells in mice.

Authors:  Shih-Wen Lin; Scott E Hensley; Nia Tatsis; Marcio O Lasaro; Hildegund C J Ertl
Journal:  J Clin Invest       Date:  2007-12       Impact factor: 14.808

Review 3.  The companions: regulatory T cells and gene therapy.

Authors:  Saman Eghtesad; Penelope A Morel; Paula R Clemens
Journal:  Immunology       Date:  2009-05       Impact factor: 7.397

Review 4.  Tolerance induction by viral in vivo gene transfer.

Authors:  Eric Dobrzynski; Roland W Herzog
Journal:  Clin Med Res       Date:  2005-11

5.  Intrinsic transgene immunogenicity gears CD8(+) T-cell priming after rAAV-mediated muscle gene transfer.

Authors:  Maxime Carpentier; Stéphanie Lorain; Pascal Chappert; Mélanie Lalfer; Romain Hardet; Dominique Urbain; Cécile Peccate; Sahil Adriouch; Luis Garcia; Jean Davoust; David-Alexandre Gross
Journal:  Mol Ther       Date:  2014-12-10       Impact factor: 11.454

6.  Tracking mesenchymal stem cell contributions to regeneration in an immunocompetent cartilage regeneration model.

Authors:  Daniela Zwolanek; María Satué; Verena Proell; José R Godoy; Kathrin I Odörfer; Magdalena Flicker; Sigrid C Hoffmann; Thomas Rülicke; Reinhold G Erben
Journal:  JCI Insight       Date:  2017-10-19

7.  Foxp3+ CD25+ regulatory T cells specific for a neo-self-antigen develop at the double-positive thymic stage.

Authors:  Julie Cabarrocas; Cécile Cassan; Fay Magnusson; Eliane Piaggio; Lennart Mars; Jens Derbinski; Bruno Kyewski; David-Alexandre Gross; Benoit L Salomon; Khashayarsha Khazaie; Abdelhadi Saoudi; Roland S Liblau
Journal:  Proc Natl Acad Sci U S A       Date:  2006-05-18       Impact factor: 11.205

8.  AAV's anatomy: roadmap for optimizing vectors for translational success.

Authors:  Angela M Mitchell; Sarah C Nicolson; Jayme K Warischalk; R Jude Samulski
Journal:  Curr Gene Ther       Date:  2010-10       Impact factor: 4.391

Review 9.  Evading the immune response upon in vivo gene therapy with viral vectors.

Authors:  Brandon K Sack; Roland W Herzog
Journal:  Curr Opin Mol Ther       Date:  2009-10

Review 10.  The Skeletal Muscle Environment and Its Role in Immunity and Tolerance to AAV Vector-Mediated Gene Transfer.

Authors:  Florence Boisgerault; Federico Mingozzi
Journal:  Curr Gene Ther       Date:  2015       Impact factor: 4.391

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.