Enhanced Transduction of Macaca fascicularis Hematopoietic Cells with Chimeric Lentiviral Vectors

• Published in: Human gene therapy Vol. 30; no. 10; p. 1306
• Main Authors: Sii-Felice, Karine, Castillo Padilla, Javier, Relouzat, Francis, Cheuzeville, Joëlle, Tantawet, Siriporn, Maouche, Leïla, Le Grand, Roger, Leboulch, Philippe, Payen, Emmanuel
• Format: Journal Article
• Language: English
• Published: United States 01.10.2019
• Subjects: Animals; Antigens, CD34 - genetics; Antigens, CD34 - immunology; Biomarkers - metabolism; Capsid - chemistry; Capsid - immunology; Female; Gene Expression; Genetic Vectors - immunology; Genetic Vectors - metabolism; Hematopoietic Stem Cell Transplantation; Hematopoietic Stem Cells - immunology; Hematopoietic Stem Cells - virology; HIV-1 - genetics; HIV-1 - immunology; Macaca fascicularis - immunology; Male; Mice; Mice, Inbred NOD; T-Lymphocytes - immunology; T-Lymphocytes - transplantation; T-Lymphocytes - virology; Transduction, Genetic - methods; Transplantation, Heterologous; Tripartite Motif Proteins - genetics; Tripartite Motif Proteins - immunology; Ubiquitin-Protein Ligases - genetics; Ubiquitin-Protein Ligases - immunology; Macaca fascicularis; nonhuman primate model; TRIM5α; lentiviral capsid; gene transfer
• ISSN: 1557-7422
• DOI: 10.1089/hum.2018.179

Recent marketing approval for genetically engineered hematopoietic stem and T cells bears witness to the substantial improvements in lentiviral vectors over the last two decades, but evaluations of the long-term efficacy and toxicity of gene and cell therapy products will, nevertheless, require further studies in nonhuman primate models. monkeys from Mauritius have a low genetic diversity and are particularly useful for reproducible drug testing. In particular, they have a genetically homogeneous class I major histocompatibility complex system that probably mitigates the variability of the response to simian immunodeficiency virus infection. However, the transduction of simian cells with human immunodeficiency virus type 1 (HIV-1)-derived vectors is inefficient due to capsid-specific restriction factors, such as the tripartite motif-containing protein tripartite motif 5α, which prevent infection with non-host-adapted retroviruses. This study introduced the modified capsid of the macaque-trophic HIV-1 clone MN4/LSQD into the packaging system and compared transduction efficiencies between hematopoietic cells transduced with this construct and cells transduced with HIV-1 NL4-3-derived packaging constructs. Capsid modification increased transduction efficiency in all hematopoietic cells tested (by factors of up to 10), including hematopoietic progenitor cells, repopulating cells, and T cells from Mauritian , regardless of vector structure or purification method. The study also established culture conditions similar to those used in clinical practice for the efficient transduction of hematopoietic stem and progenitor CD34 cells. These results suggest that the procedure is suitable for use in Mauritian , which can therefore be used as a model in preclinical studies for hematopoietic gene and cell therapy.