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囊性纤维化痰液对培养上皮细胞中腺病毒介导的基因转移的抑制作用。

Inhibitory effect of cystic fibrosis sputum on adenovirus-mediated gene transfer in cultured epithelial cells.

作者信息

Perricone M A, Rees D D, Sacks C R, Smith K A, Kaplan J M, St George J A

机构信息

Genzyme, Framingham, MA 01701, USA.

出版信息

Hum Gene Ther. 2000 Sep 20;11(14):1997-2008. doi: 10.1089/10430340050143426.

Abstract

Effective gene transfer to the airway epithelial cells of individuals with cystic fibrosis (CF) requires gene therapy vectors to effectively penetrate the mucous lining of the airways of these patients. In this study, we examined the effects of the aqueous sol fraction of sputum recovered from CF patients (CF sol) on adenovirus (Ad)-mediated gene transfer to cultured epithelial cells. Sputum collected from patients with CF was separated into aqueous sol and gel fractions by ultracentrifugation and the sol fraction from different individuals was pooled. To determine if CF sol affects Ad-mediated transfection, Fisher rat thyroid (FRT) epithelial cells or normal human bronchial epithelial (NHBE) cells were infected with an Ad encoding beta-galactosidase (Ad2/betagal-2) in the presence or absence of the pooled CF sol. Transfection efficiency was determined by measuring beta-Gal activity. CF sol significantly inhibited Ad2-mediated gene transfer in a dose-dependent manner when the vector was incubated with CF sol prior to exposure to the cells. In contrast, preincubation of the cells with the sol was without effect. The inhibition of Ad-mediated gene transfer by CF sol was not related to its low pH, was abrogated by preadsorption with an Ad2 serotype vector, and was neutralized by heat treatment, but was not affected by treatment with protease inhibitors. Analysis of CF sol fractions from seven different individuals with CF showed inhibition of Ad-mediated gene transfer in four of the seven samples tested and, further, the inhibitory effect was correlated with the presence of Ad-specific antibodies. We conclude that preexisting adenovirus-specific antibodies present in some of the patient samples were the predominant factor inhibiting Ad-mediated gene transfer.

摘要

将基因有效转移至囊性纤维化(CF)患者的气道上皮细胞,需要基因治疗载体有效穿透这些患者气道的黏液层。在本研究中,我们检测了从CF患者咳出的痰液的水溶性组分(CF溶胶)对腺病毒(Ad)介导的基因转移至培养的上皮细胞的影响。通过超速离心将CF患者咳出的痰液分离为水溶性组分和凝胶组分,并将来自不同个体的水溶性组分合并。为了确定CF溶胶是否影响Ad介导的转染,在存在或不存在合并的CF溶胶的情况下,用编码β-半乳糖苷酶的Ad(Ad2/βgal-2)感染Fisher大鼠甲状腺(FRT)上皮细胞或正常人支气管上皮(NHBE)细胞。通过测量β-半乳糖苷酶活性来确定转染效率。当载体在暴露于细胞之前与CF溶胶孵育时,CF溶胶以剂量依赖性方式显著抑制Ad2介导的基因转移。相反,细胞与该溶胶预孵育则没有效果。CF溶胶对Ad介导的基因转移的抑制作用与其低pH无关,通过用Ad2血清型载体预吸附可消除,通过热处理可中和,但不受蛋白酶抑制剂处理的影响。对来自7名不同CF患者的CF溶胶组分进行分析,结果显示在7个测试样本中有4个样本存在Ad介导的基因转移抑制,此外,抑制作用与Ad特异性抗体的存在相关。我们得出结论,一些患者样本中预先存在的腺病毒特异性抗体是抑制Ad介导的基因转移的主要因素。

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