{"title":"Alzheimer DNA Vaccine and Relativistic Time Dilation","authors":"M. Ruggiero","doi":"10.15406/jnsk.2017.07.00263","DOIUrl":null,"url":null,"abstract":"In a very recent paper published in November 2017 in the peer-reviewed scientific journal Bio Accent Open Access HIV, I describe a novel procedure designed to improve efficacy of DNA vaccines in areas as diverse as Alzheimer’s disease, HIV infection and cancer [1]. This procedure is based on non-covalent binding of highly charged molecules to DNA; positively charged polyL-lysine is first bound to plasmid DNA. This step is followed by binding of negatively charged chondroitin sulfate to the [polyL-lysine/DNA] complex in a very precise ratio. The third step consists in encasing the resulting [chondroitin sulfate/poly-Llysine/DNA] complexes in a shell of phosphatidylcholine with the formation of a structure similar to liposomes or micelles. This structure reminds the physiological assembly of phospholipids and glycosaminoglycans in human plasma as well as the primeval multi-molecular structures responsible for the origin of life on earth [2]. The implications deriving from the development of this procedure are significant for all those diseases where immunotherapy through DNA vaccination may prove useful. In the field of neurodegenerative diseases, current approaches to immunotherapy of Alzheimer’s disease, although promising, still show a number of limitations and it is anticipated that “More effective and sophisticated vaccines such as DNA vaccine and recombinant viral vaccines will be utilized in future” [3]. The procedure described in Ruggiero [1] may effectively overcome current limitations and increase efficacy of DNA vaccination in Alzheimer’s disease by providing a tool that enhances bioavailability of DNA vaccines and improves immune responses.","PeriodicalId":106839,"journal":{"name":"Journal of Neurology and Stroke","volume":"3 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2017-11-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"3","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Neurology and Stroke","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.15406/jnsk.2017.07.00263","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 3
Abstract
In a very recent paper published in November 2017 in the peer-reviewed scientific journal Bio Accent Open Access HIV, I describe a novel procedure designed to improve efficacy of DNA vaccines in areas as diverse as Alzheimer’s disease, HIV infection and cancer [1]. This procedure is based on non-covalent binding of highly charged molecules to DNA; positively charged polyL-lysine is first bound to plasmid DNA. This step is followed by binding of negatively charged chondroitin sulfate to the [polyL-lysine/DNA] complex in a very precise ratio. The third step consists in encasing the resulting [chondroitin sulfate/poly-Llysine/DNA] complexes in a shell of phosphatidylcholine with the formation of a structure similar to liposomes or micelles. This structure reminds the physiological assembly of phospholipids and glycosaminoglycans in human plasma as well as the primeval multi-molecular structures responsible for the origin of life on earth [2]. The implications deriving from the development of this procedure are significant for all those diseases where immunotherapy through DNA vaccination may prove useful. In the field of neurodegenerative diseases, current approaches to immunotherapy of Alzheimer’s disease, although promising, still show a number of limitations and it is anticipated that “More effective and sophisticated vaccines such as DNA vaccine and recombinant viral vaccines will be utilized in future” [3]. The procedure described in Ruggiero [1] may effectively overcome current limitations and increase efficacy of DNA vaccination in Alzheimer’s disease by providing a tool that enhances bioavailability of DNA vaccines and improves immune responses.
在2017年11月发表在同行评审科学期刊《Bio Accent Open Access HIV》上的一篇最新论文中,我描述了一种新的程序,旨在提高DNA疫苗在阿尔茨海默病、艾滋病毒感染和癌症等多种领域的疗效[1]。这一过程是基于高电荷分子与DNA的非共价结合;带正电的聚赖氨酸首先与质粒DNA结合。这一步之后,带负电荷的硫酸软骨素以非常精确的比例与[聚赖氨酸/DNA]复合物结合。第三步是将生成的[硫酸软骨素/聚赖氨酸/DNA]复合物包裹在磷脂酰胆碱的外壳中,形成类似脂质体或胶束的结构。这种结构让人联想到人类血浆中磷脂和糖胺聚糖的生理组装,以及地球上生命起源的原始多分子结构[2]。这一程序的发展对所有那些通过DNA疫苗免疫治疗可能证明有用的疾病具有重要意义。在神经退行性疾病领域,目前阿尔茨海默病的免疫治疗方法虽然很有前景,但仍存在一些局限性,预计“未来将使用更有效、更复杂的疫苗,如DNA疫苗和重组病毒疫苗”[3]。Ruggiero[1]所描述的程序可以通过提供一种提高DNA疫苗的生物利用度和改善免疫反应的工具,有效地克服目前的局限性,提高DNA疫苗接种在阿尔茨海默病中的疗效。