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Tetrafunctional Block Copolymers Promote Lung Gene Transfer in Newborn Piglets
- Source :
- Molecular Therapy-Nucleic Acids, Molecular Therapy-Nucleic Acids, Elsevier, 2019, 16, pp.186-193. ⟨10.1016/j.omtn.2019.02.016⟩, Molecular Therapy-Nucleic Acids, 2019, 16, pp.186-193. ⟨10.1016/j.omtn.2019.02.016⟩, Molecular Therapy-Nucleic Acids, Nature Publishing Group, 2019, 16, pp.186-193. ⟨10.1016/j.omtn.2019.02.016⟩, Molecular Therapy: Nucleic Acids, Vol 16, Iss, Pp 186-193 (2019), Molecular Therapy. Nucleic Acids, Molecular Therapy. Nucleic Acids (16), 186-193. (2019)
- Publication Year :
- 2019
- Publisher :
- HAL CCSD, 2019.
-
Abstract
- Tetrafunctional block copolymers are molecules capable of complexing DNA. Although ineffective in vitro, studies in mice have shown that the tetrafunctional block copolymer 704 is a more efficient lung gene transfer agent than the cationic liposome GL67A, previously used in a phase II clinical trial in cystic fibrosis patients. In the present study, we compared the gene transfer capacity of the 704-DNA formulation and a cationic liposome-DNA formulation equivalent to GL67A in a larger-animal model, the newborn piglet. Our results indicate an efficacy of the 704-DNA formulation well above one order of magnitude higher than that of the cationic liposome-DNA formulation, with no elevated levels of interleukin-6 (IL-6), taken as a marker of inflammation. Transgene expression was heterogeneous within lung lobes, with expression levels that were below the detection threshold in some samples, while high in other samples. This heterogeneity is likely to be due to the bolus injection procedure as well as to the small volume of injection. The present study highlights the potential of tetrafunctional block copolymers as non-viral vectors for lung gene therapy.<br />Graphical Abstract
- Subjects :
- 0301 basic medicine
copolymère
animal nouveau né
Genetic enhancement
Transgene
newborn pigs
[SDV.CAN]Life Sciences [q-bio]/Cancer
Cystic fibrosis
Article
non-viral vector
03 medical and health sciences
chemistry.chemical_compound
0302 clinical medicine
[SDV.CAN] Life Sciences [q-bio]/Cancer
Drug Discovery
Biologie animale
medicine
Cationic liposome
lungs
Animal biology
Lung
tetrafunctional block copolymers
Chemistry
lcsh:RM1-950
Cationic polymerization
medicine.disease
gene therapy
Gene transfer agent
3. Good health
thérapie génique
030104 developmental biology
medicine.anatomical_structure
transfert de gène
lcsh:Therapeutics. Pharmacology
030220 oncology & carcinogenesis
poumon
Biophysics
Molecular Medicine
porcelet
DNA
Subjects
Details
- Language :
- English
- ISSN :
- 21622531
- Database :
- OpenAIRE
- Journal :
- Molecular Therapy-Nucleic Acids, Molecular Therapy-Nucleic Acids, Elsevier, 2019, 16, pp.186-193. ⟨10.1016/j.omtn.2019.02.016⟩, Molecular Therapy-Nucleic Acids, 2019, 16, pp.186-193. ⟨10.1016/j.omtn.2019.02.016⟩, Molecular Therapy-Nucleic Acids, Nature Publishing Group, 2019, 16, pp.186-193. ⟨10.1016/j.omtn.2019.02.016⟩, Molecular Therapy: Nucleic Acids, Vol 16, Iss, Pp 186-193 (2019), Molecular Therapy. Nucleic Acids, Molecular Therapy. Nucleic Acids (16), 186-193. (2019)
- Accession number :
- edsair.doi.dedup.....b91f894ca5e4145c1a99620c1d9a4255
- Full Text :
- https://doi.org/10.1016/j.omtn.2019.02.016⟩