首页> 美国卫生研究院文献>Frontiers in Cellular and Infection Microbiology >Firewalls Prevent Systemic Dissemination of Vectors Derived from Human Adenovirus Type 5 and Suppress Production of Transgene-Encoded Antigen in a Murine Model of Oral Vaccination
【2h】

Firewalls Prevent Systemic Dissemination of Vectors Derived from Human Adenovirus Type 5 and Suppress Production of Transgene-Encoded Antigen in a Murine Model of Oral Vaccination

机译:防火墙可防止系统传播来自人类5型腺病毒的载体并抑制口服疫苗的小鼠模型中转基因编码抗原的产生。

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

To define the bottlenecks that restrict antigen expression after oral administration of viral-vectored vaccines, we tracked vectors derived from the human adenovirus type 5 at whole body, tissue, and cellular scales throughout the digestive tract in a murine model of oral delivery. After intragastric administration of vectors encoding firefly luciferase or a model antigen, detectable levels of transgene-encoded protein or mRNA were confined to the intestine, and restricted to delimited anatomical zones. Expression of luciferase in the form of multiple small bioluminescent foci in the distal ileum, cecum, and proximal colon suggested multiple crossing points. Many foci were unassociated with visible Peyer's patches, implying that transduced cells lay in proximity to villous rather than follicle-associated epithelium, as supported by detection of transgene-encoded antigen in villous epithelial cells. Transgene-encoded mRNA but not protein was readily detected in Peyer's patches, suggesting that post-transcriptional regulation of viral gene expression might limit expression of transgene-encoded antigen in this tissue. To characterize the pathways by which the vector crossed the intestinal epithelium and encountered sentinel cells, a fluorescent-labeled vector was administered to mice by the intragastric route or inoculated into ligated intestinal loops comprising a Peyer's patch. The vector adhered selectively to microfold cells in the follicle-associated epithelium, and, after translocation to the subepithelial dome region, was captured by phagocytes that expressed CD11c and lysozyme. In conclusion, although a large number of crossing events took place throughout the intestine within and without Peyer's patches, multiple firewalls prevented systemic dissemination of vector and suppressed production of transgene-encoded protein in Peyer's patches.
机译:为了确定口服病毒载体疫苗后限制抗原表达的瓶颈,我们在口服给药的鼠模型中,在整个消化道中追踪了人体5型腺病毒衍生的载体在整个消化道的整体,组织和细胞水平。在胃内施用编码萤火虫荧光素酶或模型抗原的载体后,可检测水平的转基因编码蛋白或mRNA被限制在肠道内,并限制在限定的解剖区域内。荧光素酶在回肠末端,盲肠和近端结肠中以多个小生物发光灶的形式表达,提示存在多个交叉点。许多病灶与可见的Peyer斑片无关,这表明转导的细胞位于绒毛而不是与卵泡相关的上皮附近,这​​是在绒毛上皮细胞中检测到转基因编码抗原所支持的。在Peyer斑块中很容易检测到转基因编码的mRNA,但未检测到蛋白质,表明病毒基因表达的转录后调控可能会限制该组织中转基因编码抗原的表达。为了表征载体穿过肠上皮并遇到前哨细胞的途径,通过胃内途径将荧光标记的载体施用于小鼠或接种到包含派伊尔氏膜的结扎肠环中。该载体选择性粘附在与卵泡相关的上皮中的微折叠细胞上,并在转移到上皮下圆顶区后被表达CD11c和溶菌酶的吞噬细胞捕获。总之,尽管在整个肠道内都发生了许多跨过事件,无论是否存在Peyer斑块,但多个防火墙阻止了载体的系统传播,并抑制了Peyer斑块中转基因编码蛋白的产生。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号