Sustained and therapeutic delivery of factor IX in nude haemophilia B mice by encapsulated C2C12 myoblasts: concurrent tumourigenesis

• Published in: Haemophilia : the official journal of the World Federation of Hemophilia 2001-03, Vol.7 (2), p.207-214
• Main Authors: Hortelano, G., Wang, L., Xu, N., Ofosu, F. A.
• Format: Article
• Language: English
• Subjects: Animals; C2C12 myoblast; Capsules; factor IX; Factor IX - administration & dosage; Factor IX - genetics; Factor IX - secretion; gene therapy; Genetic Therapy - methods; haemophilia B; Hemophilia B - drug therapy; Mice; Mice, Mutant Strains; Mice, Nude; microcapsules; Partial Thromboplastin Time; Time Factors; Transfection; Tumor Cells, Cultured - secretion
• ISSN: 1351-8216; 1365-2516
• DOI: 10.1046/j.1365-2516.2001.00492.x

This study reports the generation of an immunodeficient murine model for haemophilia B, obtained by breeding factor IX‐deficient mice with an immunodeficient mouse strain, and use of this mouse model to evaluate the long‐term efficacy and safety of a gene therapy strategy for treating haemophilia B. Nude haemophilic mice were implanted with biocompatible microcapsules enclosing recombinant myoblasts secreting human factor IX. The activated partial thromboplastin time (APTT) of plasma of mice thus treated was invariably shortened 3 weeks after microcapsule implantation, and remained shortened for at least 77 days. Shortening of the APTT of the haemophilia mice coincided with the appearance of human factor IX in mice plasmas (up to 600 ng mL−1 on day 77), and normalization of the tail‐bleeding time. Thus, the microencapsulated myoblasts reversed the clinical phenotype of haemophilia B. In contrast, plasmas of immunocompetent haemophilic mice similarly implanted with microcapsules only showed a transient shortening of APTT, and coincident transient delivery of human factor IX antigen. Rapid disappearance of human factor IX from plasmas of immunocompetent mice also coincided with production of antibodies to the human transgene. Significantly, 86% of the nude haemophilia mice developed tumours of myoblast origin. Thus, while this study revealed the feasibility of this gene therapy approach to treat severe haemophilia B, it also highlights the importance of using safer cell lines to prevent tumour development.