Cargando…
Differential effects of periodontal microbiome on the rheumatoid factor induction during rheumatoid arthritis pathogenesis
Association between exposure to periodontal bacteria and development of autoantibodies related to rheumatoid arthritis (RA) has been widely accepted; however, direct causal relationship between periodontal bacteria and rheumatoid factor (RF) is currently not fully understood. We investigated whether...
Autores principales: | , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9668994/ https://www.ncbi.nlm.nih.gov/pubmed/36385263 http://dx.doi.org/10.1038/s41598-022-21788-y |
_version_ | 1784832034514927616 |
---|---|
author | Kim, Ji-Won Jung, Hyerin Baek, In-Pyo Nam, Yoojun Kang, Jaewoo Chung, Min Kyung Park, Jun-Beom Lee, Jennifer Kwok, Seung-Ki Kim, Wan-Uk Park, Sung-Hwan Ju, Ji Hyeon |
author_facet | Kim, Ji-Won Jung, Hyerin Baek, In-Pyo Nam, Yoojun Kang, Jaewoo Chung, Min Kyung Park, Jun-Beom Lee, Jennifer Kwok, Seung-Ki Kim, Wan-Uk Park, Sung-Hwan Ju, Ji Hyeon |
author_sort | Kim, Ji-Won |
collection | PubMed |
description | Association between exposure to periodontal bacteria and development of autoantibodies related to rheumatoid arthritis (RA) has been widely accepted; however, direct causal relationship between periodontal bacteria and rheumatoid factor (RF) is currently not fully understood. We investigated whether periodontal bacteria could affect RF status. Patients with preclinical, new-onset, or chronic RA underwent periodontal examination, and investigation of subgingival microbiome via 16S rRNA sequencing. Degree of arthritis and RF induction was examined in collagen-induced arthritis (CIA) mice that were orally inoculated with different periodontal bacteria species. Subsequently, single-cell RNA sequencing analysis of the mouse spleen cells was performed. Patients with preclinical RA showed an increased abundance of the Porphyromonadacae family in the subgingival microbiome compared to those with new-onset or chronic RA, despite comparable periodontitis severity among them. Notably, a distinct subgingival microbial community was found between patients with high-positive RF and those with negative or low-positive RF (p=0.022). Oral infections with the periodontal pathogens P. gingivalis and Treponema denticola in CIA mice similarly enhanced arthritis score, but resulted in different levels of RF induction. Genes related to B cell receptor signaling, B cell proliferation, activation, and differentiation, and CD4(+) T cell costimulation and cytokine production were involved in the differential induction of RF in mice exposed to different bacteria. In summary, periodontal microbiome might shape RF status by affecting the humoral immune response during RA pathogenesis. |
format | Online Article Text |
id | pubmed-9668994 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-96689942022-11-18 Differential effects of periodontal microbiome on the rheumatoid factor induction during rheumatoid arthritis pathogenesis Kim, Ji-Won Jung, Hyerin Baek, In-Pyo Nam, Yoojun Kang, Jaewoo Chung, Min Kyung Park, Jun-Beom Lee, Jennifer Kwok, Seung-Ki Kim, Wan-Uk Park, Sung-Hwan Ju, Ji Hyeon Sci Rep Article Association between exposure to periodontal bacteria and development of autoantibodies related to rheumatoid arthritis (RA) has been widely accepted; however, direct causal relationship between periodontal bacteria and rheumatoid factor (RF) is currently not fully understood. We investigated whether periodontal bacteria could affect RF status. Patients with preclinical, new-onset, or chronic RA underwent periodontal examination, and investigation of subgingival microbiome via 16S rRNA sequencing. Degree of arthritis and RF induction was examined in collagen-induced arthritis (CIA) mice that were orally inoculated with different periodontal bacteria species. Subsequently, single-cell RNA sequencing analysis of the mouse spleen cells was performed. Patients with preclinical RA showed an increased abundance of the Porphyromonadacae family in the subgingival microbiome compared to those with new-onset or chronic RA, despite comparable periodontitis severity among them. Notably, a distinct subgingival microbial community was found between patients with high-positive RF and those with negative or low-positive RF (p=0.022). Oral infections with the periodontal pathogens P. gingivalis and Treponema denticola in CIA mice similarly enhanced arthritis score, but resulted in different levels of RF induction. Genes related to B cell receptor signaling, B cell proliferation, activation, and differentiation, and CD4(+) T cell costimulation and cytokine production were involved in the differential induction of RF in mice exposed to different bacteria. In summary, periodontal microbiome might shape RF status by affecting the humoral immune response during RA pathogenesis. Nature Publishing Group UK 2022-11-16 /pmc/articles/PMC9668994/ /pubmed/36385263 http://dx.doi.org/10.1038/s41598-022-21788-y Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Kim, Ji-Won Jung, Hyerin Baek, In-Pyo Nam, Yoojun Kang, Jaewoo Chung, Min Kyung Park, Jun-Beom Lee, Jennifer Kwok, Seung-Ki Kim, Wan-Uk Park, Sung-Hwan Ju, Ji Hyeon Differential effects of periodontal microbiome on the rheumatoid factor induction during rheumatoid arthritis pathogenesis |
title | Differential effects of periodontal microbiome on the rheumatoid factor induction during rheumatoid arthritis pathogenesis |
title_full | Differential effects of periodontal microbiome on the rheumatoid factor induction during rheumatoid arthritis pathogenesis |
title_fullStr | Differential effects of periodontal microbiome on the rheumatoid factor induction during rheumatoid arthritis pathogenesis |
title_full_unstemmed | Differential effects of periodontal microbiome on the rheumatoid factor induction during rheumatoid arthritis pathogenesis |
title_short | Differential effects of periodontal microbiome on the rheumatoid factor induction during rheumatoid arthritis pathogenesis |
title_sort | differential effects of periodontal microbiome on the rheumatoid factor induction during rheumatoid arthritis pathogenesis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9668994/ https://www.ncbi.nlm.nih.gov/pubmed/36385263 http://dx.doi.org/10.1038/s41598-022-21788-y |
work_keys_str_mv | AT kimjiwon differentialeffectsofperiodontalmicrobiomeontherheumatoidfactorinductionduringrheumatoidarthritispathogenesis AT junghyerin differentialeffectsofperiodontalmicrobiomeontherheumatoidfactorinductionduringrheumatoidarthritispathogenesis AT baekinpyo differentialeffectsofperiodontalmicrobiomeontherheumatoidfactorinductionduringrheumatoidarthritispathogenesis AT namyoojun differentialeffectsofperiodontalmicrobiomeontherheumatoidfactorinductionduringrheumatoidarthritispathogenesis AT kangjaewoo differentialeffectsofperiodontalmicrobiomeontherheumatoidfactorinductionduringrheumatoidarthritispathogenesis AT chungminkyung differentialeffectsofperiodontalmicrobiomeontherheumatoidfactorinductionduringrheumatoidarthritispathogenesis AT parkjunbeom differentialeffectsofperiodontalmicrobiomeontherheumatoidfactorinductionduringrheumatoidarthritispathogenesis AT leejennifer differentialeffectsofperiodontalmicrobiomeontherheumatoidfactorinductionduringrheumatoidarthritispathogenesis AT kwokseungki differentialeffectsofperiodontalmicrobiomeontherheumatoidfactorinductionduringrheumatoidarthritispathogenesis AT kimwanuk differentialeffectsofperiodontalmicrobiomeontherheumatoidfactorinductionduringrheumatoidarthritispathogenesis AT parksunghwan differentialeffectsofperiodontalmicrobiomeontherheumatoidfactorinductionduringrheumatoidarthritispathogenesis AT jujihyeon differentialeffectsofperiodontalmicrobiomeontherheumatoidfactorinductionduringrheumatoidarthritispathogenesis |