Immunomodulation Mediated by Azithromycin in Experimental Periapical Inflammation

被引:23
作者
Andrada, Ana Cristina [1 ,2 ]
Azuma, Mariane Maffei [4 ]
Furusho, Hisako [5 ]
Hirai, Kimito [4 ,6 ,7 ]
Xu, Shuang [6 ,8 ]
White, Robert R. [2 ]
Sasaki, Hajime [3 ,4 ,6 ]
机构
[1] Univ Detroit, Mercy Sch Dent, Div Endodont, Dept Essentials & Simulat, Detroit, MI USA
[2] Harvard Sch Dent Med, Div Endodont, Dept Restorat Dent & Biomat Sci, Boston, MA USA
[3] Harvard Sch Dent Med, Dept Oral Med Infect & Immun, Boston, MA USA
[4] Univ Michigan, Sch Dent, Dept Cariol Restorat Sci & Endodont, 1011 North Univ Ave, Ann Arbor, MI 48109 USA
[5] Hiroshima Univ, Dept Oral & Maxillofacial Pathobiol, Hiroshima, Japan
[6] Forsyth Inst, Dept Immunol & Infect Dis, Cambridge, MA USA
[7] Okayama Univ, Dept Periodont & Endodont, Sch Dent, Kita Ku, Okayama, Japan
[8] Brigham & Womens Hosp, Funct Genom Lab, Channing Div Network Med, 75 Francis St, Boston, MA 02115 USA
基金
美国国家卫生研究院;
关键词
Ampicillin; azithromycin; endodontic infection; immunomodulation; periapical periodontitis; BONE DESTRUCTION; INFECTION; MACROLIDE; MICE;
D O I
10.1016/j.joen.2020.07.028
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Introduction: The purpose of the present study was to compare the immunomodulatory effect of azithromycin (AZM), ampicillin (AMP), amoxicillin (AMX), and clindamycin (CLI) in vitro and AZM on preexisting periapical lesions compared with AMP. Methods: The susceptibility of 4 common human endodontic pathogens (Parvimonas micra, Streptococcus intermedius, Prevotella intermedia, and Fusobacterium nucleatum) to AZM, AMP, AMX, and CLI was confirmed by agar disk diffusion assay. Preexisting periapical lesions in C57BL/6J mice were treated with AZM, AMP, or phosphate-buffered saline (PBS). Periapical bone healing and the pattern of inflammatory cell infiltration were evaluated after a 10-day treatment by micro-computed tomographic and histology, respectively. Besides, the effect of antibiotics in pathogen-stimulated nuclear factor kappa B activation and the production of interleukin 1 alpha and tumor necrosis factor alpha was assessed in vitro by luciferase assay and enzyme linked immunosorbent assay. Results: All examined endodontic pathogens were susceptible to AZM, AMP, AMX, and CLI. AZM significantly attenuated periapical bone loss versus PBS. PBS resulted in widely diffused infiltration of mixed inflammatory cells. By contrast, AZM brought about localized infiltration of neutrophils and M2 macrophages and advanced fibrosis. Although the effect of AMP on bone was uncertain, inflammatory cell infiltration was considerably milder than PBS. However, most macrophages observed seemed to be M1 macrophages. AZM suppressed pathogen-stimulated nuclear factor kappa B activation and cytokine production, whereas AMP, AMX, and CLI reduced only cytokine production moderately. Conclusions: This study showed that AZM led to the resolution of preexisting experimental periapical inflammation. Our data provide a perspective on host response in antibiotic selection for endodontic treatment. However, well-designed clinical trials are necessary to better elucidate the benefits of AZM as an adjunctive therapy for endodontic treatment when antibiotic therapy is recommended. Although both AZM and AMP were effective on preexisting periapical lesions, AZM led to advanced wound healing, probably depending on its immunomodulatory effect.
引用
收藏
页码:1648 / 1654
页数:7
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