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本文引用的文献

1
High-level expression of human lactoferrin in the milk of goats by using replication-defective adenoviral vectors.利用复制缺陷型腺病毒载体在山羊乳汁中高效表达人乳铁蛋白。
Protein Expr Purif. 2007 May;53(1):225-31. doi: 10.1016/j.pep.2006.11.019. Epub 2006 Dec 8.
2
Chick embryo lethal orphan virus can be polymer-coated and retargeted to infect mammalian cells.鸡胚致死孤儿病毒可以进行聚合物包被并重新靶向以感染哺乳动物细胞。
Gene Ther. 2006 Feb;13(4):356-68. doi: 10.1038/sj.gt.3302655.
3
Engineering conditionally replication-competent adenoviral vectors carrying the cytosine deaminase gene increases the infectivity and therapeutic effect for breast cancer gene therapy.携带胞嘧啶脱氨酶基因的工程化条件性复制腺病毒载体可提高乳腺癌基因治疗的感染性和治疗效果。
Cancer Gene Ther. 2006 Apr;13(4):346-56. doi: 10.1038/sj.cgt.7700906.
4
Deletion of penton RGD motifs affects the efficiency of both the internalization and the endosome escape of viral particles containing adenovirus serotype 5 or 35 fiber knobs.删除五邻体RGD基序会影响含有5型或35型腺病毒纤维钮的病毒颗粒的内化效率和从内体逃逸的效率。
J Virol. 2005 Jan;79(2):1053-61. doi: 10.1128/JVI.79.2.1053-1061.2005.
5
High-level expression of the coxsackievirus and adenovirus receptor messenger RNA in osteosarcoma, Ewing's sarcoma, and benign neurogenic tumors among musculoskeletal tumors.柯萨奇病毒和腺病毒受体信使核糖核酸在骨肉瘤、尤因肉瘤及肌肉骨骼肿瘤中的良性神经源性肿瘤中的高表达。
Clin Cancer Res. 2004 Jun 1;10(11):3831-8. doi: 10.1158/1078-0432.CCR-03-0345.
6
Avian adenovirus CELO recombinants expressing VP2 of infectious bursal disease virus induce protection against bursal disease in chickens.表达传染性法氏囊病病毒VP2的禽腺病毒CELO重组体可诱导鸡对法氏囊病产生保护作用。
Vaccine. 2004 Jun 2;22(17-18):2351-60. doi: 10.1016/j.vaccine.2003.10.039.
7
Recombinant avian adenovirus CELO expressing the human interleukin-2: characterization in vitro, in ovo and in vivo.表达人白细胞介素-2的重组禽腺病毒CELO:体外、卵内和体内特性研究
Virus Res. 2004 Mar 15;100(2):257-61. doi: 10.1016/j.virusres.2003.11.018.
8
Restoration of p53 tumor-suppressor activity in human tumor cells in vitro and in their xenografts in vivo by recombinant avian adenovirus CELO-p53.通过重组禽腺病毒CELO-p53在体外人肿瘤细胞及其体内异种移植瘤中恢复p53肿瘤抑制活性。
Gene Ther. 2004 Jan;11(1):79-84. doi: 10.1038/sj.gt.3302146.
9
Adenoviral gene therapy for cancer: from vectors to targeted and replication competent agents (review).用于癌症治疗的腺病毒基因疗法:从载体到靶向性及具有复制能力的药物(综述)
Int J Oncol. 2002 Dec;21(6):1161-74.
10
Treatment of ovarian cancer with a tropism modified oncolytic adenovirus.用嗜性修饰的溶瘤腺病毒治疗卵巢癌。
Cancer Res. 2002 Mar 1;62(5):1266-70.

鉴定CELO腺病毒纤维中类似HI的环以纳入受体结合基序。

Identification of HI-like loop in CELO adenovirus fiber for incorporation of receptor binding motifs.

作者信息

Logunov Denis Y, Zubkova Olga V, Karyagina-Zhulina Anna S, Shuvalova Eugenia A, Karpov Andrei P, Shmarov Maxim M, Tutykhina Irina L, Alyapkina Yulia S, Grezina Natalia M, Zinovieva Natalia A, Ernst Lev K, Gintsburg Alexsandr L, Naroditsky Boris S

机构信息

Gamaleya Research Institute for Epidemiology and Microbiology (GIEM), 123098, Gamaleya Street 18, Moscow, Russia.

出版信息

J Virol. 2007 Sep;81(18):9641-52. doi: 10.1128/JVI.00534-07. Epub 2007 Jun 27.

DOI:10.1128/JVI.00534-07
PMID:17596306
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2045437/
Abstract

Vectors based on the chicken embryo lethal orphan (CELO) avian adenovirus (Ad) have two attractive properties for gene transfer applications: resistance to preformed immune responses to human Ads and the ability to grow in chicken embryos, allowing low-cost production of recombinant viruses. However, a major limitation of this technology is that CELO vectors demonstrate decreased efficiency of gene transfer into cells expressing low levels of the coxsackie-Ad receptor (CAR). In order to improve the efficacy of gene transfer into CAR-deficient cells, we modified viral tropism via genetic alteration of the CELO fiber 1 protein. The alphav integrin-binding motif (RGD) was incorporated at two different sites of the fiber 1 knob domain, within an HI-like loop that we identified and at the C terminus. Recombinant fiber-modified CELO viruses were constructed containing secreted alkaline phosphatase (SEAP) and enhanced green fluorescent protein genes as reporter genes. Our data show that insertion of the RGD motif within the HI-like loop of the fiber resulted in significant enhancement of gene transfer into CAR-negative and CAR-deficient cells. In contrast, CELO vectors containing the RGD motif at the fiber 1 C terminus showed reduced transduction of all cell lines. CELO viruses modified with RGD at the HI-like loop transduced the SEAP reporter gene into rabbit mammary gland cells in vivo with an efficiency significantly greater than that of unmodified CELO vector and similar to that of Ad type 5 vector. These results illustrate the potential for efficient CELO-mediated gene transfer into a broad range of cell types through modification of the identified HI-like loop of the fiber 1 protein.

摘要

基于鸡胚致死孤儿(CELO)禽腺病毒(Ad)的载体在基因转移应用方面具有两个吸引人的特性:对人腺病毒的预先形成的免疫反应具有抗性,以及能够在鸡胚中生长,从而实现重组病毒的低成本生产。然而,该技术的一个主要局限性是,CELO载体在将基因转移到表达低水平柯萨奇腺病毒受体(CAR)的细胞中时,效率会降低。为了提高基因转移到CAR缺陷细胞中的效率,我们通过对CELO纤维1蛋白进行基因改造来改变病毒嗜性。αv整合素结合基序(RGD)被引入到纤维1球状结构域的两个不同位点,一个在我们鉴定出的类似HI的环内,另一个在C末端。构建了含有分泌碱性磷酸酶(SEAP)和增强型绿色荧光蛋白基因作为报告基因的重组纤维修饰CELO病毒。我们的数据表明,在纤维的类似HI的环内插入RGD基序可显著提高基因转移到CAR阴性和CAR缺陷细胞中的效率。相比之下,在纤维1 C末端含有RGD基序的CELO载体对所有细胞系的转导效率都降低。在类似HI的环处用RGD修饰的CELO病毒在体内将SEAP报告基因转导到兔乳腺细胞中的效率明显高于未修饰的CELO载体,且与5型腺病毒载体相似。这些结果说明了通过修饰鉴定出的纤维1蛋白的类似HI的环,CELO介导的基因高效转移到广泛细胞类型中的潜力。