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用于肠道递送人白细胞介素10的基因工程乳酸乳球菌的生物遏制

Biological containment of genetically modified Lactococcus lactis for intestinal delivery of human interleukin 10.

作者信息

Steidler Lothar, Neirynck Sabine, Huyghebaert Nathalie, Snoeck Veerle, Vermeire An, Goddeeris Bruno, Cox Eric, Remon Jean Paul, Remaut Erik

机构信息

Department of Molecular Biomedical Research, Vlaams Interuniversitair instituut voor Biotechnologie, Ghent University, KL. Ledeganckstraat 35, B-9000 Ghent, Belgium.

出版信息

Nat Biotechnol. 2003 Jul;21(7):785-9. doi: 10.1038/nbt840. Epub 2003 Jun 15.

Abstract

Genetically modified Lactococcus lactis secreting interleukin 10 provides a therapeutic approach for inflammatory bowel disease. However, the release of such genetically modified organisms through clinical use raises safety concerns. In an effort to address this problem, we replaced the thymidylate synthase gene thyA of L. lactis with a synthetic human IL10 gene. This thyA- hIL10+ L. lactis strain produced human IL-10 (hIL-10), and when deprived of thymidine or thymine, its viability dropped by several orders of magnitude, essentially preventing its accumulation in the environment. The biological containment system and the bacterium's capacity to secrete hIL-10 were validated in vivo in pigs. Our approach is a promising one for transgene containment because, in the unlikely event that the engineered L. lactis strain acquired an intact thyA gene from a donor such as L. lactis subsp. cremoris, the transgene would be eliminated from the genome.

摘要

分泌白细胞介素10的转基因乳酸乳球菌为炎症性肠病提供了一种治疗方法。然而,通过临床使用释放此类转基因生物引发了安全担忧。为了解决这个问题,我们用合成的人IL10基因取代了乳酸乳球菌的胸苷酸合成酶基因thyA。这种thyA - hIL10 +乳酸乳球菌菌株产生人IL - 10(hIL - 10),当缺乏胸苷或胸腺嘧啶时,其活力下降几个数量级,基本上阻止了其在环境中的积累。这种生物遏制系统以及该细菌分泌hIL - 10的能力在猪体内得到了验证。我们的方法对于转基因遏制来说是一种很有前景的方法,因为在不太可能发生的情况下,即工程化的乳酸乳球菌菌株从诸如乳酸乳球菌亚种cremoris这样的供体获得完整的thyA基因时,转基因将从基因组中消除。

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