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Erschienen in: Archivum Immunologiae et Therapiae Experimentalis 4/2011

01.08.2011 | ORIGINAL ARTICLE

Soluble TNF-α Receptor I Encoded on Plasmid Vector and Its Application in Experimental Gene Therapy of Radiation-Induced Lung Fibrosis

verfasst von: Małgorzata Przybyszewska, Joanna Miłoszewska, Sylwia Rzońca, Halina Trembacz, Kazimiera Pyśniak, Agnieszka Kotlarz, Paweł Swoboda, Marta Zalewska, Maciej Małecki

Erschienen in: Archivum Immunologiae et Therapiae Experimentalis | Ausgabe 4/2011

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Abstract

Post-radiation inflammatory reaction leads to an irreversible pulmonary fibrosis which may cause lethal respiratory insufficiency. Pathological inflammatory and fibrotic changes might be attenuated by inhibiting tumour necrosis factor (TNF)-α activity using TNF-α soluble receptors. Thus, an experimental antifibrotic gene therapy with the plasmid vector encoding a mouse soluble receptor I for TNF-α (psTNFR-I) was assessed. Soluble TNFR-I encoding gene was cloned into pcDNA3.1 plasmid. The ability of psTNFR-I expressing vector to transfect cells, and its biological activity in vitro and in vivo were examined by PCR, RT-PCR, MTT assay and ELISA. The C57Bl/6J mice received single intramuscular injection of psTNFR-I, conjugated with polyetylenimine (PEI) 25 kDa, equally divided to both hind legs, 3 days before irradiation (20 Gy, Co60), and either a single injection or ten injections once a week after irradiation. The data proved the effectiveness of psTNFR-I product to neutralise TNF-α activity in vitro. The in vivo plasmid incorporation and maintenance was confirmed. Measurements of plasma soluble TNFR-I levels showed that the in vivo gene transfer was effective. PEI was found to enhance transfection efficiency in vivo. The psTNFR-I/PEI complexes caused no toxicity in the transfected mice. C57Bl/6J mice that received prolonged psTNFR-I/PEI injections developed lethal fibrotic syndrome and died 8 weeks later than the mice treated with a double plasmid injection and the control mice treated with a control plasmid. Sequential administration of soluble TNFR-I by a nonviral, intramuscular gene transduction in the early and late post-radiation inflammatory phase prolonged survival of irradiated mice and attenuated the symptoms of lung fibrosis. The psTNFR-I gene transduction may provide a safe and simple method to partially neutralise TNF-α activity and prevent radiation-induced lung injury.
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Metadaten
Titel
Soluble TNF-α Receptor I Encoded on Plasmid Vector and Its Application in Experimental Gene Therapy of Radiation-Induced Lung Fibrosis
verfasst von
Małgorzata Przybyszewska
Joanna Miłoszewska
Sylwia Rzońca
Halina Trembacz
Kazimiera Pyśniak
Agnieszka Kotlarz
Paweł Swoboda
Marta Zalewska
Maciej Małecki
Publikationsdatum
01.08.2011
Verlag
SP Birkhäuser Verlag Basel
Erschienen in
Archivum Immunologiae et Therapiae Experimentalis / Ausgabe 4/2011
Print ISSN: 0004-069X
Elektronische ISSN: 1661-4917
DOI
https://doi.org/10.1007/s00005-011-0133-2