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A Recoding Method to Improve the Humoral Immune Response to an HIV DNA Vaccine

机译:一种提高对HIV DNA疫苗的体液免疫反应的编码方法

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摘要

This manuscript describes a novel strategy to improve HIV DNA vaccine design. Employing a new information theory based bioinformatic algorithm, we identify a set of nucleotide motifs which are common in the coding region of HIV, but are under-represented in genes that are highly expressed in the human genome. We hypothesize that these motifs contribute to the poor protein expression of gag, pol, and env genes from the c-DNAs of HIV clinical isolates. Using this approach and beginning with a codon optimized consensus gag gene, we recode the nucleotide sequence so as to remove these motifs without modifying the amino acid sequence. Transfecting the recoded DNA sequence into a human kidney cell line results in doubling the gag protein expression level compared to the codon optimized version. We then turn both sequences into DNA vaccines and compare induced antibody response in a murine model. Our sequence, which has the motifs removed, induces a five-fold increase in gag antibody response compared to the codon optimized vaccine.
机译:该手稿描述了一种改进HIV DNA疫苗设计的新颖策略。我们采用一种新的基于信息论的生物信息学算法,确定了一组核苷酸基序,这些基序在HIV的编码区中很常见,但在人类基因组中高度表达的基因中却没有得到很好的体现。我们假设这些基序导致了来自HIV临床分离株c-DNA的gag,pol和env基因的蛋白质表达不佳。使用这种方法并从密码子优化的共有gag基因开始,我们重新编码核苷酸序列,以便在不修饰氨基酸序列的情况下去除这些基序。与密码子优化版本相比,将重新编码的DNA序列转染到人肾细胞系中会使gag蛋白表达水平翻倍。然后,我们将两个序列都变成DNA疫苗,并在鼠模型中比较诱导的抗体反应。与密码子优化疫苗相比,去除了基序的我们的序列可诱导gag抗体反应提高五倍。

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