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Porphyromonas, Treponema, and Mogibacterium promote IL8/IFNγ/TNFα-based pro-inflammation in patients with medication-related osteonecrosis of the jaw.
Li, Qingxiang; Pu, Yinfei; Lu, Han; Zhao, Ning; Wang, Yifei; Guo, Yuxing; Guo, Chuanbin.
Afiliação
  • Li Q; Department of Oral and Maxillofacial Surgery, Peking University School and Hospital of Stomatology, Beijing, PR China.
  • Pu Y; National Clinical Research Center for Oral Diseases, Beijing, PR China.
  • Lu H; National Engineering Laboratory for Digital and Material Technology of Stomatology, Beijing, PR China.
  • Zhao N; Beijing Key Laboratory of Digital Stomatology, Peking University School and Hospital of Stomatology, Beijing, PR China.
  • Wang Y; Department of Oral and Maxillofacial Surgery, Peking University School and Hospital of Stomatology, Beijing, PR China.
  • Guo Y; National Clinical Research Center for Oral Diseases, Beijing, PR China.
  • Guo C; National Engineering Laboratory for Digital and Material Technology of Stomatology, Beijing, PR China.
J Oral Microbiol ; 13(1): 1851112, 2020 Nov 23.
Article em En | MEDLINE | ID: mdl-33391627
ABSTRACT

Objective:

Refractory infection is an important factor affecting the progression of medication-related osteonecrosis of the jaw (MRONJ) from clinical stage I to stage II/III. The aim of this study was to explore the distribution of bacteria and their association with the inflammatory pathway of stage II/III MRONJ. Materials and

Methods:

Nine specimens of fresh inflammation tissue, located next to the necrotic bone or sequestrum, were collected from MRONJ patients. Nine specimens from normal oral mucosa were collected from healthy patients. The 16S rRNA gene sequencing method was used to determine the distribution characteristics of the bacterial colony. The protein microarray analysis was used to detect the expression of inflammatory cytokines.

Results:

The average relative abundance of Bacteroidetes, Spirochaetes, Synergistetes, and Tenericutes was higher, while Proteobacteria and Actinobacteria were lower in the MRONJ group. Most pro-inflammatory cytokines were up-regulated in the MRONJ group; yet, only IFNγ, TNFα, and IL8 showed statistical differences (P < 0.05). Porphyromonas and Treponema were positively correlated with IL8, and Mogibacterium was positively correlated with IFNγ and TNFα.

Conclusions:

IL8/IFNγ/TNFα pro-inflammatory effect caused by Porphyromonas, Treponema, and Mogibacterium may be the leading cause of advancing MRONJ and thus may be used as a new target for infection control.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2020 Tipo de documento: Article