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Updated: Jul 5, 2026

Lentiviral Vector Preparation for Efficient Gene and MicroRNA Modulation of Peritoneal Cavity Tissue-Resident Macrophages In Vivo in Mice
Published on: February 16, 2024
Liposome vectors for in vivo gene delivery
1University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
Abstract:
Gene therapy with nonviral, cationic liposome-based vectors has demonstrated promising results in a variety of in vivo models and some clinical trials. In contrast to viral vectors, cationic liposome-based vectors usually induce just mild inflammatory reactions, making them suitable for repeated injections in animals. This unit describes the preparation and delivery of two liposome-based vectors Gene therapy with nonviral, cationic liposome-based vectors has demonstrated promising results in a variety of in vivo models.
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