Preclinical study of mutagenicity and safety of a vaccine against pneumococcal infection based on a recombinant hybrid protein

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Abstract

Pneumococcal infection is the cause of pneumo-nia. Vaccination can prevent the severe course of this disease. The pneumococcal vaccine considered in the work was created by a genetically modified method based on a hybrid recombinant protein. The aim of the work was preclinical investigation of the mutagenic, genetic safety of the new pneumococcal vaccine, Irivax, against pneumococcal infection in rats. Materials and methods. Studies of the Irivax vaccine were carried out in male Wistar rats’ cell populations of the bone marrow and peripheral blood mononuclear cells. The karyoty-pic stability of cells and myelogram of the bone mar-row were studied. Results. After the introduction of the vaccine, the content of the lymphoid germ cells in the blood of rats was increased to 74.2% (p <0.05), which proves the body’s immune response. The frequency of cells with an unstable genome, as an indicator of the genetic safety of the AL-vaccine, was rare both in expe-rimental and control animals, and did not exceed 1.5%. Conclusion. Thus, the new pneumococcal vaccine Irivax and its components have mutagenic and toxic safety.
基于重组杂交蛋白的肺炎球菌感染疫苗的致突变性和安全性临床前研究
肺炎球菌感染是肺炎的病因。接种疫苗可以预防这种疾病的严重发展。研究中考虑的肺炎球菌疫苗是通过基于杂交重组蛋白的转基因方法制造的。这项工作的目的是临床前研究新的肺炎球菌疫苗Irivax对大鼠肺炎球菌感染的诱变性和遗传安全性。材料和方法。Irivax疫苗的研究是在雄性Wistar大鼠的骨髓细胞群和外周血单核细胞群中进行的。研究了细胞的核生化稳定性和骨髓的骨髓显影。结果。接种疫苗后,大鼠血液中淋巴生殖细胞的含量增加到74.2% (p <0.05),证明机体免疫应答。作为al -疫苗遗传安全性指标的不稳定基因组细胞的频率在实验动物和对照动物中都很少见,不超过1.5%。结论。因此,新型肺炎球菌疫苗Irivax及其组分具有致突变性和毒性安全性。
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