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Immunosuppression by FK506 markedly prolongs expression of adenovirus-delivered transgene in skeletal muscles of adult dystrophic [mdx] mice.

作者信息

Lochmüller H, Petrof B J, Allen C, Prescott S, Massie B, Karpati G

机构信息

Montreal Neurological Institute, McGill University, Quebec, Canada.

出版信息

Biochem Biophys Res Commun. 1995 Aug 15;213(2):569-74. doi: 10.1006/bbrc.1995.2169.

DOI:10.1006/bbrc.1995.2169
PMID:7544122
Abstract

Adenovirus-mediated gene transfer into skeletal muscles of adult immune competent animals has been limited by the fact that a cellular immune attack of the host against transduced muscle fibers prevented long-term transgene expression. In this study we treated adult dystrophic [mdx] mice with daily subcutaneous injections of the immunosuppressive drug FK506 (tacrolimus) over 10 and 30 days after adenovirus-mediated reporter gene transfer and compared the transduction level to saline-injected controls. After 30 days, transgene expression was no longer demonstrable in the control group, whereas it remained at about 70% of the 10-day transduction value in the FK506 treated group. In addition, we demonstrated a reduction in the number of CD3 and CD8 positive T-lymphocytes in the muscles of the immunosuppressed group compared to controls.

摘要

相似文献

1
Immunosuppression by FK506 markedly prolongs expression of adenovirus-delivered transgene in skeletal muscles of adult dystrophic [mdx] mice.
Biochem Biophys Res Commun. 1995 Aug 15;213(2):569-74. doi: 10.1006/bbrc.1995.2169.
2
Transient immunosuppression by FK506 permits a sustained high-level dystrophin expression after adenovirus-mediated dystrophin minigene transfer to skeletal muscles of adult dystrophic (mdx) mice.通过FK506进行的短暂免疫抑制,在腺病毒介导的肌营养不良蛋白小基因转移至成年营养不良(mdx)小鼠的骨骼肌后,可使肌营养不良蛋白持续高水平表达。
Gene Ther. 1996 Aug;3(8):706-16.
3
Adeno-associated virus vector-mediated gene transfer into dystrophin-deficient skeletal muscles evokes enhanced immune response against the transgene product.腺相关病毒载体介导的基因转移至缺乏抗肌萎缩蛋白的骨骼肌中会引发针对转基因产物的免疫反应增强。
Gene Ther. 2002 Dec;9(23):1576-88. doi: 10.1038/sj.gt.3301829.
4
Ex vivo gene transfer using adenovirus-mediated full-length dystrophin delivery to dystrophic muscles.使用腺病毒介导的全长抗肌萎缩蛋白递送至营养不良肌肉的体外基因转移。
Gene Ther. 1998 Jan;5(1):19-30. doi: 10.1038/sj.gt.3300549.
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Adenovirus-mediated dystrophin minigene transfer improves muscle strength in adult dystrophic (MDX) mice.腺病毒介导的肌营养不良蛋白小基因转移可改善成年营养不良(MDX)小鼠的肌肉力量。
Gene Ther. 1998 Mar;5(3):369-79. doi: 10.1038/sj.gt.3300600.
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Immune evasion by muscle-specific gene expression in dystrophic muscle.营养不良性肌肉中通过肌肉特异性基因表达实现免疫逃逸。
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Very efficient myoblast allotransplantation in mice under FK506 immunosuppression.在FK506免疫抑制下,小鼠体内成肌细胞同种异体移植效率极高。
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FK506 immunosuppression to control the immune reactions triggered by first-generation adenovirus-mediated gene transfer.使用FK506免疫抑制来控制第一代腺病毒介导的基因转移引发的免疫反应。
Hum Gene Ther. 1995 Nov;6(11):1391-401. doi: 10.1089/hum.1995.6.11-1391.
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The short MCK1350 promoter/enhancer allows for sufficient dystrophin expression in skeletal muscles of mdx mice.
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Long-term reversal of hypercholesterolemia in low density lipoprotein receptor (LDLR)-deficient mice by adenovirus-mediated LDLR gene transfer combined with CD154 blockade.通过腺病毒介导的低密度脂蛋白受体(LDLR)基因转移联合CD154阻断,使低密度脂蛋白受体(LDLR)缺陷小鼠的高胆固醇血症长期逆转。
J Gene Med. 2000 Jan-Feb;2(1):41-51. doi: 10.1002/(SICI)1521-2254(200001/02)2:1<41::AID-JGM79>3.0.CO;2-P.

引用本文的文献

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Four decades of adenovirus gene transfer vectors: History and current use.腺病毒基因转移载体四十年:历史与当前应用
Mol Ther. 2025 May 7;33(5):2192-2204. doi: 10.1016/j.ymthe.2025.03.062. Epub 2025 Apr 2.
2
Progress in gene therapy for Duchenne muscular dystrophy.
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3
Application of a Fas ligand encoding a recombinant adenovirus vector for prolongation of transgene expression.应用编码Fas配体的重组腺病毒载体延长转基因表达。
J Virol. 1998 Mar;72(3):2483-90. doi: 10.1128/JVI.72.3.2483-2490.1998.
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Persistence in muscle of an adenoviral vector that lacks all viral genes.一种缺乏所有病毒基因的腺病毒载体在肌肉中的持久性。
Proc Natl Acad Sci U S A. 1997 Mar 4;94(5):1645-50. doi: 10.1073/pnas.94.5.1645.