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体内 RNA 转染产生抗体。

Antibody production by in vivo RNA transfection.

机构信息

Cellular and Molecular Research Center (CMRC), Faculty of Medicine, Ahvaz Jundishapur University of Medical Sciences (AJUMS), Ahvaz, 61357-15794, Iran.

Department of Biology, Faculty of Science, University of Isfahan, Isfahan, 81746-73441, Iran.

出版信息

Sci Rep. 2017 Sep 7;7(1):10863. doi: 10.1038/s41598-017-11399-3.

Abstract

Monoclonal antibodies have a variety of applications in research and medicine. Here, we report development of a new method for production of monoclonal antibodies. Our method relies on in vivo RNA transfection rather than peptide vaccination. We took advantage of RNA transcripts complexed with DOTMA and DOPE lipids to transfect mice. Intravenous administration of our RNA vaccine to mice resulted in expression of the antigenic peptides by splenic dendritic cells and detection of the antigens in the serum. The RNA vaccine stimulated production of specific antibodies against the RNA-encoded peptides. We produced monoclonal antibodies against viral, bacterial, and human antigens. In addition, we showed that our RNA vaccine stimulated humoral immunity and rescued mice infected with influenza A virus. Our method could be used as an efficient tool to generate monoclonal antibodies and to stimulate humoral immunity for research and medical purposes.

摘要

单克隆抗体在研究和医学中有多种应用。在这里,我们报告了一种生产单克隆抗体的新方法。我们的方法依赖于体内 RNA 转染而不是肽疫苗接种。我们利用与 DOTMA 和 DOPE 脂质复合的 RNA 转录本转染小鼠。将我们的 RNA 疫苗静脉注射到小鼠中,导致脾树突状细胞表达抗原肽,并在血清中检测到抗原。RNA 疫苗刺激针对 RNA 编码肽的特异性抗体的产生。我们生产了针对病毒、细菌和人类抗原的单克隆抗体。此外,我们表明,我们的 RNA 疫苗刺激了体液免疫,并拯救了感染甲型流感病毒的小鼠。我们的方法可用于作为一种有效的工具来产生单克隆抗体并刺激用于研究和医疗目的的体液免疫。

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