Oğuz Ferdi, Atmaca Harika
Section of Molecular Biology, Department of Biology, Institute of Natural and Applied Sciences, Manisa Celal Bayar University, Muradiye, Manisa, Turkey.
Section of Molecular Biology, Department of Biology, Faculty of Science and Letters, Manisa Celal Bayar University, Muradiye, Manisa, Turkey.
Adv Pharm Bull. 2022 Mar;12(2):274-282. doi: 10.34172/apb.2022.028. Epub 2021 May 16.
Vaccination is one of the important approaches in the prevention and control of diseases. Although the capacity to present antigens other than the disease-specific antigen in the traditional vaccine composition provides a potential benefit by increasing its protective efficacy, many components that are not needed for the related disease are also transferred. These components can reduce vaccine activity by lowering immunity against protective antigens. The reasons such as the low effectiveness of traditional vaccines and the high cost of production and time-consuming reasons show that it is necessary to develop a new vaccine method for our world, which is struggling with epidemics almost every year. Among nucleic acids, mRNA has many advantages, such as genomic integration, induction of anti-DNA autoantibodies, and immune tolerance induced by long-term antigen expression. mRNA vaccines have become a therapeutic target for reasons such as efficacy, safety, fast and non-expensive production. The fact that mRNA triggers both humoral and cellular immunity and goes only to the cytoplasm, not to the nucleus, makes it highly efficient. The mRNA must cross the lipid bilayer barrier and entry to the cytoplasm where it is translated into protein. There are two main ways of mRNA vaccine delivery for this: ex vivo loading of mRNA into dendritic cells (DCs) and direct injection of mRNA with or without a carrier. Studies continue to understand which delivery system is therapeutically more efficient. Preclinical and clinical trials showed that mRNA vaccines trigger a long-lasting and safe immune response.
疫苗接种是疾病预防和控制的重要手段之一。尽管传统疫苗组合物中呈现疾病特异性抗原以外的抗原的能力通过提高其保护效力提供了潜在益处,但许多与相关疾病无关的成分也会被传递。这些成分会通过降低对保护性抗原的免疫力来降低疫苗活性。传统疫苗有效性低、生产成本高以及耗时等原因表明,对于几乎每年都在与流行病作斗争的我们的世界而言,开发一种新的疫苗方法是必要的。在核酸中,信使核糖核酸(mRNA)具有许多优势,例如基因组整合、诱导抗DNA自身抗体以及长期抗原表达诱导的免疫耐受。由于有效性、安全性、生产快速且成本低等原因,mRNA疫苗已成为一个治疗靶点。mRNA既能触发体液免疫又能触发细胞免疫,并且仅进入细胞质而非细胞核,这使其具有高效性。mRNA必须穿过脂质双层屏障并进入细胞质,在那里它被翻译成蛋白质。为此,mRNA疫苗递送主要有两种方式:将mRNA体外加载到树突状细胞(DC)中以及直接注射有或没有载体的mRNA。研究仍在继续,以了解哪种递送系统在治疗上更有效。临床前和临床试验表明,mRNA疫苗能触发持久且安全的免疫反应。