Autlan Regional Hospital, Health Secretariat, Autlan 48900, Jalisco, Mexico; Biology Laboratory, Autlan Regional Preparatory School, University of Guadalajara, Autlan 48900, Jalisco, Mexico.
University of Lincoln, Brayford Pool, Lincoln, Lincolnshire LN6 7TS, United Kingdom.
Int J Biol Macromol. 2024 May;267(Pt 1):131427. doi: 10.1016/j.ijbiomac.2024.131427. Epub 2024 Apr 5.
Due to the health emergency created by SARS-CoV-2, the virus that causes the COVID-19 disease, the rapid implementation of a new vaccine technology was necessary. mRNA vaccines, being one of the cutting-edge new technologies, attracted significant interest and offered a lot of hope. The potential of these vaccines in preventing admission to hospitals and serious illness in people with comorbidities has recently been called into question due to the vaccines' rapidly waning immunity. Mounting evidence indicates that these vaccines, like many others, do not generate sterilizing immunity, leaving people vulnerable to recurrent infections. Additionally, it has been discovered that the mRNA vaccines inhibit essential immunological pathways, thus impairing early interferon signaling. Within the framework of COVID-19 vaccination, this inhibition ensures an appropriate spike protein synthesis and a reduced immune activation. Evidence is provided that adding 100 % of N1-methyl-pseudouridine (m1Ψ) to the mRNA vaccine in a melanoma model stimulated cancer growth and metastasis, while non-modified mRNA vaccines induced opposite results, thus suggesting that COVID-19 mRNA vaccines could aid cancer development. Based on this compelling evidence, we suggest that future clinical trials for cancers or infectious diseases should not use mRNA vaccines with a 100 % m1Ψ modification, but rather ones with the lower percentage of m1Ψ modification to avoid immune suppression.
由于 SARS-CoV-2 病毒引起的 COVID-19 疾病所造成的健康紧急情况,有必要快速实施一种新的疫苗技术。mRNA 疫苗作为一种前沿的新技术,引起了极大的关注,并带来了很大的希望。由于这些疫苗的免疫迅速减弱,其预防住院和慢性病患者发生严重疾病的潜力最近受到了质疑。越来越多的证据表明,这些疫苗和许多其他疫苗一样,不会产生能完全阻止再次感染的免疫性,并且发现 mRNA 疫苗抑制了重要的免疫途径,从而损害了早期干扰素信号。在 COVID-19 疫苗接种框架内,这种抑制作用确保了适当的刺突蛋白合成和减少免疫激活。有证据表明,在黑色素瘤模型中,将 100%的 N1-甲基假尿嘧啶(m1Ψ)添加到 mRNA 疫苗中会刺激癌症生长和转移,而未经修饰的 mRNA 疫苗则会产生相反的结果,这表明 COVID-19 mRNA 疫苗可能会促进癌症发展。基于这一有力证据,我们建议未来用于癌症或传染病的临床试验不应使用 100% m1Ψ 修饰的 mRNA 疫苗,而应使用修饰程度较低的 mRNA 疫苗,以避免免疫抑制。