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在活鼠体内持久靶向 B 淋巴细胞。

Durable targeting of B-lymphocytes in living mice.

机构信息

Department of Microbiology & Immunology, University of Michigan, 1150 W, Medical Center Dr., Ann Arbor, MI, 48109-5656, USA.

Department of Surgery, University of Michigan, 1150 W, Medical Center Dr., Ann Arbor, MI, 48109-5656, USA.

出版信息

Sci Rep. 2018 Jul 24;8(1):11143. doi: 10.1038/s41598-018-29452-0.

Abstract

Transfer to and enduring expression of genes in B cells has proved a vexing challenge. We report here a novel method for the specific and durable targeting of B lymphocytes in living mice. The method involves generation of lentiviruses pseudotyped with an anti-CD19 antibody. CD19 targeting viruses injected in the spleen of living mice efficiently transduced B cells and plasma cells detected by flow cytometry analysis of GFP expression. Expression of the reporter gene could be detected in the intact animal by external imaging for more than a year and was enhanced by booster immunization. Our method thus enables the specific delivery, expression and localization by external imaging of exogenous genes to the B cells and plasma cells of living individuals.

摘要

将基因转移并持久表达到 B 细胞一直是一个令人困扰的挑战。我们在此报告一种在活体小鼠中特异性且持久地靶向 B 淋巴细胞的新方法。该方法涉及生成带有抗 CD19 抗体的假型慢病毒。通过流式细胞术分析 GFP 表达,活体小鼠脾脏内注射的 CD19 靶向病毒可有效转导 B 细胞和浆细胞。通过外部成像,在完整动物体内可检测到报告基因的表达超过一年,并且通过加强免疫可增强表达。因此,我们的方法可以将外源基因特异性地递送到活体个体的 B 细胞和浆细胞中,并通过外部成像进行表达和定位。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/03c9/6057982/c3975cb1d0d9/41598_2018_29452_Fig1_HTML.jpg

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