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[PMID]: | 29194752 |
[Au] Autor: | Engen SA; Schreurs O; Petersen F; Blix IJS; Baekkevold ES; Schenck K |
[Ad] Endereço: | Department of Oral Biology, Faculty of Dentistry, University of Oslo, Oslo, Norway. |
[Ti] Título: | The Regulatory Role of the Oral Commensal Streptococcus mitis on Human Monocytes. |
[So] Source: | Scand J Immunol;87(2):80-87, 2018 Feb. | [Is] ISSN: | 1365-3083 |
[Cp] País de publicação: | England |
[La] Idioma: | eng |
[Ab] Resumo: | Streptococcus mitis colonizes all niches of the human oral cavity from early infancy and throughout life. Monocytes patrol blood vessels, lymphoid and non-lymphoid tissues and migrate into infected tissue where they participate in the inflammatory cascade and immune regulation. Here, we studied the effect of S. mitis on monocytes. Transcriptome analysis of monocytes exposed to S. mitis (SmMo) revealed increased transcription of chemotactic factors (CCL2, CCL3, CCL20, CXCL1, CXCL2) and cytokines (IL1A, IL1B, IL6, IL23, IL36G, TNF), indicating that S. mitis may trigger recruitment of leucocytes and initiate inflammation. Increased transcription in SmMo of IL1B, IL6 and IL23 indicated that S. mitis may participate in the induction of Th17 responses and agreed with our earlier findings of S. mitis-mediated memory Th17 reactivity. Furthermore, S. mitis inhibited tetanus toxoid-specific CD4 T cell proliferation. This can be due to the increased secretion of IL-10 and expression of PD-L1 that was observed in SmMo. PGE2 can modulate IL-10 and PD-L1 expression, concomitant with that of CCR7, IL-12 and IL-23 that also were changed. This, along with increased SmMo transcription of PTGS2 (COX2) and PTGER4 (EP4), pointed to a role of PGE2. Measurement of PGE2 secretion by SmMo showed indeed a marked increase, and chemical inhibition of PGE2 production lowered the PD-L1 expression on SmMo. In conclusion, our findings show that S. mitis may trigger immune modulation by recruiting immune cells to the site of infection, while at the same time dampening the severity of the response through expression of IL-10, PGE2 and PD-L1. |
[Mh] Termos MeSH primário: |
Monócitos/imunologia Boca/microbiologia Infecções Estreptocócicas/imunologia Streptococcus mitis/imunologia
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[Mh] Termos MeSH secundário: |
Antígeno B7-H1/metabolismo Células Cultivadas Quimiotaxia Ciclo-Oxigenase 2/genética Ciclo-Oxigenase 2/metabolismo Citocinas/genética Citocinas/metabolismo Dinoprostona/metabolismo Perfilação da Expressão Gênica Regulação da Expressão Gênica Seres Humanos Imunomodulação Mediadores da Inflamação/metabolismo Monócitos/microbiologia Receptores de Prostaglandina E Subtipo EP4/genética Receptores de Prostaglandina E Subtipo EP4/metabolismo Simbiose
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[Pt] Tipo de publicação: | JOURNAL ARTICLE |
[Nm] Nome de substância:
| 0 (B7-H1 Antigen); 0 (Cytokines); 0 (Inflammation Mediators); 0 (PTGER4 protein, human); 0 (Receptors, Prostaglandin E, EP4 Subtype); EC 1.14.99.1 (Cyclooxygenase 2); EC 1.14.99.1 (PTGS2 protein, human); K7Q1JQR04M (Dinoprostone) |
[Em] Mês de entrada: | 1802 |
[Cu] Atualização por classe: | 180206 |
[Lr] Data última revisão:
| 180206 |
[Sb] Subgrupo de revista: | IM |
[Da] Data de entrada para processamento: | 171202 |
[St] Status: | MEDLINE |
[do] DOI: | 10.1111/sji.12636 |
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