お待たせしました。ようやく、槐耳臨床研究第二期第四弾論文が掲載されました。
槐耳（カイジ）が、新型コロナウイルス感染患者の治癒に非常な効果を示したという画期的な論文です。同時に、日本を含めた世界中で使用されたファイザー・バイオテックのmRNAワクチンがウイルス自体を産生し、槐耳（カイジ）がそれに対する防御および抑制を全RNAシークエンス解析により発見した論文であるため、なかなか掲載に至らず、ようやく掲載の運びになった次第です。
掲載は2023年1月24日です。
Background
Although striking effects of vaccination strategy against pandemic COVID-19, a long-term influence by repeated partial virus mRNA injections are unknown. In addition, the molecular mechanism in accelerated ageing process still remains unclear. Through our clinical research, we observe and reported spontaneous SARS-CoV-2 virion and virion part production after Pfizer-BioNTech mRNA vaccination, observed from 3 weeks after the first injection. A significant destruction in ribosomal RNA structures, enhanced by repeated vaccinations, were also identified. The present study is aimed to define molecular mechanisms for SARS-CoV-2 virion production after injection of mRNA vaccination with a comparison to virion proliferation in non-vaccinated patient with severe COVID-19 pneumonia and fibrosis.
Methods
We direct clinical research to define molecular basis for significant anti-cancer efficacy of Huaier (Trametes robiniophila murr). In the present study, we used peripheral blood samples from the volunteer patient, suspected lung cancer by CT image analysis with age-matched normal controls with or without Huaier administration. Molecular characterization was performed analyzed by total RNA and non-coding small RNA sequencing on BGISEQ-500 Platform (about 7.0 GB analysis per sample). Thorough genetic events, Gene Ontology analysis, and functional target gene analysis were performed by using KEGG pathway classification (https://www.genome.jp/kegg/) .
Results
Spontaneous SARS-CoV-2 virion production was identified after Pfizer-BioNTech mRNA vaccination until even 5 months after the 3rdvaccination. We compared this virion production in vivo with infected virus proliferation from severe COVID-19 pneumonia case without any vaccination by total RNA sequencing. No virion and virion particle were detected in normal control with continuous Huaier administration for two years, and in the completely recovered after 3 month treatment only with 30 g per day Huaier. In contrast, without Huaier, the latent and increasing virion production was detected proportionally to the extent of the progressive destruction of the ribosomal RNAs. Molecular mechanisms demonstrated were dependent on genomic potential to rescue the functional control on perturbed kinase regulation through the integrated mTOR/PI3K/AKT pathway network, with massive mi- and piRNA-mediated transcriptional control. Even though specific small RNAs or transcriptional factors were identified, the present study clearly demonstrated SARS-CoV-2 virion production (whole and part) by repeated partial SARS-CoV-2 mRNA vaccination.
Conclusions
The present study clearly demonstrated SARS-CoV-2 virion production (whole and part) by repeated partial SARS-CoV-2 mRNA vaccination. Extensive genomic potential with massive up/downregulation of mi- and piRNAs were identified, too, but no specific small RNAs or transcriptional factors were detected. It is emphasized the significant efficacy of Huaier on the rescue of disrupted ribosomal RNA structure, on the elimination of spontaneous production of virion and virion part in vivo, and on the restoration of the regulatory kinase functions, which in total might affect the accelerated ageing processes in COVID-19. These results are encouraging to provide effective adjuvant therapy, toward the up-coming postpandemic COVID-19 era.
次回のブログでは、抄録の日本語訳を掲載予定です。