Laboratory Animal and Comparative Medicine ›› 2020, Vol. 40 ›› Issue (4): 332-.DOI: 10.3969/j.issn.1674-5817.2020.04.008

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Inhibting Effects of Cytomegalovirus on Partial Immune Index of Mice Implanted with Methacrylate

JIANG Rong1, ZHANG Qimei2   

  1. 1. Department of Dental, People's Hospital of Aba Tibetan and Qiang Autonomous Prefecture, Aba Tibetan and Qiang Autonomous Prefecture 624000, China;
    2. Department of Periodontal Mucosa, Southwest Medical University Affiliated Stomatological Hospital, Luzhou 646000, China
  • Received:2020-03-13 Online:2020-08-25 Published:2020-11-20

Abstract:  Objective    To study the effect of cytomegalovirus (CMV) on the immune response after polymethyl methacrylate (PMMA) implantation. Methods    A mouse model of CMV infection was constructed by intraperitoneal injection. After 7 days of inoculation, PMMA was implanted into the subcutaneous of back in mice. The proportion of monocytes / macrophages, CD4+T cells, CD8+T cells and regulatory T cells (Treg cells) in peripheral blood was detected by flow cytometry, and the concentrations of tumor necrosis factor-alpha (TNF-α) and interleukin -1β (IL-1β) were detected by enzyme-linked immunosorbent assay (ELISA). Results    Compared with the implantation control group, the proportion of M1 mononuclear / macrophages in peripheral blood decreased by 73.18% (t=5.896, P=0.004), the proportion of M2 monocytes / macrophages increased by 2.18 times (t=7.971, P=0.001), and the CD4+/CD8+T cell ratio decreased by 42.91% (t=6.468, P=0.003), while the Treg cell proportion increased by 2.49 times (t=4.495, P=0.011). Compared with the implanted control group, the concentrations of TNF-α and IL-1β in peripheral blood of implanted CMV group were reduced by 71.65% and 57.95% (t=7.236, P=0.019; t=7.543, P=0.002), respectively. Conclusion    The CMV can significantly inhibit the immune response after PPMA implantation, which provides theory evidence for the treatment of CMV-infected patients after oral biomaterials implantation.

Key words: Cytomegalovirus, Oral implant materials, Immunosuppression, Polymethyl methacrylate

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