抗sars - cov -2 mRNA疫苗接种后破坏性核糖体RNA结构功能补偿的怀尔效应

Manami Tanaka, Tomoo Tanaka, Xiaolong Zhu, Fei Teng, Hong Lin, Zhu-Quan Luo, Ying Pan, S. Sadahiro, Toshiyuki Suzuki, Y. Maeda, Ding Wei, Zheng Lu
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引用次数: 2

摘要

尽管针对COVID-19的疫苗接种策略在世界范围内产生了显著效果,但序次注射病毒mRNA的长期影响尚不清楚。我们通过总RNA测序分析了接种了辉瑞- biontech疫苗的正常健康志愿者和接受或不接受辅助怀尔治疗的癌症患者的生物学变化。发现了核糖体RNA结构的显著破坏,通过连续射击增强了这种破坏。与铂(II)复合物化疗引起的破坏不同,18S核糖体的进行性破坏甚至在接种后6个月就被发现。这种影响导致翻译和转录的大量抑制,特别是在与衰老过程相关的神经内/神经间信号传递和脂质代谢中。怀尔通过mirna介导的转录控制,通过典型的PI3K/AKT信号通路激活来补偿这些功能障碍。基因本体论分析显示,即使在第一次接种疫苗3个月后,自发产生的病毒粒子数量也有所增加。目前的研究表明,像怀尔这样的辅助治疗通过mRNA接种来补偿加速的衰老过程。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Huaier Effects on Functional Compensation with Destructive Ribosomal RNA Structure after Anti-SARS-CoV-2 mRNA Vaccination
Although striking effects of vaccination strategy against COVID-19 world-wide, a long-term influence by sequential viral mRNA injections are unknown. We analysed biological alterations by total RNA sequencing in Pfizer-BioNTech vaccinated normal healthy volunteers and cancer patients, with or without adjuvant Huaier therapy. A significant destruction in ribosomal RNA structures was identified, enhanced by serial shots. Unlike the destruction caused by chemotherapy with platinum (II) complex, progressive destruction in 18S ribosome was identified even at 6 months after vaccination. The influence resulted in massive inhibition of translation and transcription, significantly in intra/inter neural signaling transfer and in lipid metabolism, related to ageing process. Huaier compensated these dysfunctions by miRNA-mediated transcriptional control, by typical activation in PI3K/AKT signaling pathway. Gene Ontology analysis revealed spontaneous virion production in number even after 3 months of the first vaccination. Present study indicated that the adjuvant therapy like Huaier compensates accelerated ageing process by mRNA vaccination.
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