Transient gene therapy to treat cutaneous radiation syndrome: development in a 
minipig model

Riccobono, D.; Forcheron, F.; Agay, D.; Scherthan, H.; Meineke, V.; Drouet, M.

doi:10.1097/HP.0000000000000099

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Transient gene therapy to treat cutaneous radiation syndrome: development in a minipig model

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Scherthan, H.
Dept. of Human Molecular Genetics (Head: Hans-Hilger Ropers), Max Planck Institute for Molecular Genetics, Max Planck Society;
Institut für Radiobiologie der Bundeswehr, Neuherbergstraße 11, 80937 München, Germany;

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http://www.ncbi.nlm.nih.gov/pubmed/24776904
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引用

Riccobono, D., Forcheron, F., Agay, D., Scherthan, H., Meineke, V., & Drouet, M. (2014). Transient gene therapy to treat cutaneous radiation syndrome: development in a minipig model. Health Physics, 106(6), 713-719. doi:10.1097/HP.0000000000000099.

引用: https://hdl.handle.net/11858/00-001M-0000-0025-C0D6-E

要旨

Cutaneous radiation syndrome is the delayed consequence of localized skin exposure to high doses of ionizing radiation. Adipocyte derived stem cells injection may improve tissue regeneration through secreted factors. Thus mesenchymal stem cells secretome optimization, using transient transfection, may represent a new strategy to treat this syndrome. Sonic hedgehog, a secreted protein involved in cell proliferation and angiogenesis, has been chosen as a first candidate. Here preliminary results are reported of the therapeutic potential of transient gene therapy to cure cutaneous radiation syndrome in a minipig model. Adipocyte derived stem cells were transiently transfected by electroporation with a plasmid coding for Sonic Hedgehog. Gottingen minipigs were locally irradiated using a (60)Co gamma source at the dose of 50 Gy and received Phosphate Buffer Salin (controls: n = 8), stem cells (50 x 10(6) each time, n = 5) or transfected stem cells (25+/-7 x 10(6) each time, n = 1). All controls exhibited a homogeneous clinical evolution of cutaneous radiation syndrome with final necrosis (day 91). In stem cell injected minipigs, an ultimate wound healing was observed in four out of five grafted animals (day 130 +/- 28, complete in two of them) (historical results). The Sonic hedgehog animal, albeit injected with a lower number of transfected stem cells, presented a very similar evolution of skin healing without necrosis or uncontrolble pain. Globally this preliminary report suggests that local injection of Sonic Hedgehog transfected adipocyte derived stem cells may improve wound healing. Thus work is ongoing to evaluate this therapeutic strategy on a larger number of animals.