Alexyuk Madina S, Bogoyavlenskiy Andrey P, Zaitseva Irina A, Omirtaeva Elmira S, Moldakhanov Yergali S, Akanova Kuralay S, Anarkulova Elmira I, Berezin Vladimir E, Alexyuk Pavel G
Research and Production Center for Microbiology and Virology, Almaty, Kazakhstan.
Research and Production Center for Microbiology and Virology, Almaty, Kazakhstan.
Virus Res. 2025 Jul 19;359:199610. doi: 10.1016/j.virusres.2025.199610.
With the global spread of bacterial resistance and the decreasing effectiveness of antibiotics, the relevance of phage therapy is constantly growing. However, for systemic use of bacteriophages in medical practice, a complete understanding of their interaction not only with bacterial cells but also with human and animal organisms in the context of co-administered therapy is required. This article presents the studies into the effects of lytic Escherichia coli bacteriophages on various immune response factors after their intraperitoneal administration in mice. It was found using Real-Time PCR and ELISA methods that the administration of the vB_EcoM_SCS4 and vB_EcoM_SCS57 phages did not increase the gene expression of TLR3, TLR9, IL-4, IL-5, IL-6 and the concentration of IL-2, IL-4, IL-5 and IL-6 in mice, but led to a multi-fold increase in the gene expression and concentration of IFNγ. Whereas, the injection of the vB_EcoS_SCS44 phage into mice increased the expression of the studied genes, except for the IL-5 gene, by 4 to 7 times and increased the concentration of IL-2, IL-4, IL-6 and IFNγ, except for IL-5, by 2 to 3 times. When determining the titer of virus-specific antibodies, it was found that after the administration of phages vB_EcoM_SCS4 and vB_EcoM_SCS57, the titer of IgA, IgG and IgM did not differ from that of the control animals, but the administration of phage vB_EcoS_SCS44 stimulated a twofold increase in the titer of phage-specific IgA, IgG, IgM.
随着细菌耐药性在全球范围内的传播以及抗生素有效性的降低,噬菌体疗法的相关性不断增加。然而,对于在医学实践中全身使用噬菌体,不仅需要全面了解它们与细菌细胞的相互作用,还需要了解在联合治疗背景下它们与人和动物机体的相互作用。本文介绍了溶菌性大肠杆菌噬菌体腹腔注射小鼠后对各种免疫反应因子影响的研究。使用实时荧光定量聚合酶链反应(Real-Time PCR)和酶联免疫吸附测定(ELISA)方法发现,vB_EcoM_SCS4和vB_EcoM_SCS57噬菌体的给药并未增加小鼠体内Toll样受体3(TLR3)、Toll样受体9(TLR9)、白细胞介素4(IL-4)、白细胞介素5(IL-5)、白细胞介素6(IL-6)的基因表达以及白细胞介素2(IL-2)、IL-4、IL-5和IL-6的浓度,但导致干扰素γ(IFNγ)的基因表达和浓度增加了数倍。而向小鼠注射vB_EcoS_SCS44噬菌体使所研究基因(白细胞介素5基因除外)的表达增加了4至7倍,并使IL-2、IL-4、IL-6和IFNγ(IL-5除外)的浓度增加了2至3倍。在测定病毒特异性抗体滴度时发现,给予噬菌体vB_EcoM_SCS4和vB_EcoM_SCS57后,免疫球蛋白A(IgA)、免疫球蛋白G(IgG)和免疫球蛋白M(IgM)的滴度与对照动物无差异,但给予噬菌体vB_EcoS_SCS44刺激了噬菌体特异性IgA、IgG、IgM滴度的两倍增加。
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