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In Utero Transfer of Adeno-Associated Viral Vectors Produces Long-Term Factor IX Levels in a Cynomolgus Macaque Model.
Mattar, Citra N Z; Gil-Farina, Irene; Rosales, Cecilia; Johana, Nuryanti; Tan, Yvonne Yi Wan; McIntosh, Jenny; Kaeppel, Christine; Waddington, Simon N; Biswas, Arijit; Choolani, Mahesh; Schmidt, Manfred; Nathwani, Amit C; Chan, Jerry K Y.
Afiliación
  • Mattar CNZ; Obstetrics & Gynaecology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore 119077, Singapore. Electronic address: citramattar@nus.edu.sgp.
  • Gil-Farina I; Department of Translational Oncology, German Cancer Research Center and National Center for Tumor Diseases, 69120 Heidelberg, Germany.
  • Rosales C; UCL Cancer Institute, University College London, London WC1E 6BT, United Kingdom.
  • Johana N; Reproductive Medicine, K.K. Women's and Children's Hospital, Singapore 229899, Singapore.
  • Tan YYW; Reproductive Medicine, K.K. Women's and Children's Hospital, Singapore 229899, Singapore.
  • McIntosh J; UCL Cancer Institute, University College London, London WC1E 6BT, United Kingdom.
  • Kaeppel C; Department of Translational Oncology, German Cancer Research Center and National Center for Tumor Diseases, 69120 Heidelberg, Germany.
  • Waddington SN; Institute for Women's Health, University College London, London WC1E 6BT, United Kingdom; MRC Antiviral Gene Therapy Research Unit, Faculty of Health Sciences, University of the Witwatersrand, Johannesburg 2000, South Africa.
  • Biswas A; Obstetrics & Gynaecology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore 119077, Singapore.
  • Choolani M; Obstetrics & Gynaecology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore 119077, Singapore.
  • Schmidt M; Department of Translational Oncology, German Cancer Research Center and National Center for Tumor Diseases, 69120 Heidelberg, Germany.
  • Nathwani AC; UCL Cancer Institute, University College London, London WC1E 6BT, United Kingdom.
  • Chan JKY; Reproductive Medicine, K.K. Women's and Children's Hospital, Singapore 229899, Singapore; Duke-NUS Medical School, Singapore 169857, Singapore. Electronic address: jerrychan@nus.edu.sg.
Mol Ther ; 25(8): 1843-1853, 2017 08 02.
Article en En | MEDLINE | ID: mdl-28462816
The safe correction of an inherited bleeding disorder in utero prior to the onset of organ damage is highly desirable. Here, we report long-term transgene expression over more than 6 years without toxicity following a single intrauterine gene transfer (IUGT) at 0.9G using recombinant adeno-associated vector (AAV)-human factor IX (hFIX) in the non-human primate model we have previously described. Four of six treated animals monitored for around 74 months expressed hFIX at therapeutic levels (3.9%-120.0%). Long-term expression was 6-fold higher in males and with AAV8 compared to AAV5, mediated almost completely at this stage by random genome-wide hepatic proviral integrations, with no evidence of hotspots. Post-natal AAV challenge without immunosuppression was evaluated in two animals exhibiting chronic low transgene expression. The brief neutralizing immune reaction elicited had no adverse effect and, although expression was not improved at the dose administered, no clinical toxicity was observed. This long-term surveillance thus confirms the safety of late-gestation AAV-hFIX transfer and demonstrates that postnatal re-administration can be performed without immunosuppression, although it requires dose optimization for the desired expression. Nevertheless, eventual vector genotoxicity and the possibility of germline transmission will require lifelong monitoring and further evaluation of the reproductive function of treated animals.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Factor IX / Expresión Génica / Hemofilia B / Técnicas de Transferencia de Gen / Dependovirus / Vectores Genéticos Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Animals / Female / Humans / Male / Pregnancy Idioma: En Revista: Mol Ther Asunto de la revista: BIOLOGIA MOLECULAR / TERAPEUTICA Año: 2017 Tipo del documento: Article Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Factor IX / Expresión Génica / Hemofilia B / Técnicas de Transferencia de Gen / Dependovirus / Vectores Genéticos Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Animals / Female / Humans / Male / Pregnancy Idioma: En Revista: Mol Ther Asunto de la revista: BIOLOGIA MOLECULAR / TERAPEUTICA Año: 2017 Tipo del documento: Article Pais de publicación: Estados Unidos