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High percentages and activity of synovial fluid NK cells present in patients with advanced stage active Rheumatoid Arthritis
Rheumatoid Arthritis (RA) causes chronic inflammation of joints. The cytokines TNFα and IFNγ are central players in RA, however their source has not been fully elucidated. Natural Killer (NK) cells are best known for their role in elimination of viral-infected and transformed cells, and they secrete...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6361912/ https://www.ncbi.nlm.nih.gov/pubmed/30718650 http://dx.doi.org/10.1038/s41598-018-37448-z |
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author | Yamin, Rachel Berhani, Orit Peleg, Hagit Aamar, Suhail Stein, Natan Gamliel, Moriya Hindi, Issam Scheiman-Elazary, Anat Gur, Chamutal |
author_facet | Yamin, Rachel Berhani, Orit Peleg, Hagit Aamar, Suhail Stein, Natan Gamliel, Moriya Hindi, Issam Scheiman-Elazary, Anat Gur, Chamutal |
author_sort | Yamin, Rachel |
collection | PubMed |
description | Rheumatoid Arthritis (RA) causes chronic inflammation of joints. The cytokines TNFα and IFNγ are central players in RA, however their source has not been fully elucidated. Natural Killer (NK) cells are best known for their role in elimination of viral-infected and transformed cells, and they secrete pro-inflammatory cytokines. NK cells are present in the synovial fluids (SFs) of RA patients and are considered to be important in bone destruction. However, the phenotype and function of NK cells in the SFs of patients with erosive deformative RA (DRA) versus non-deformative RA (NDRA) is poorly characterized. Here we characterize the NK cell populations present in the blood and SFs of DRA and NDRA patients. We demonstrate that a distinct population of activated synovial fluid NK (sfNK) cells constitutes a large proportion of immune cells found in the SFs of DRA patients. We discovered that although sfNK cells in both DRA and NDRA patients have similar phenotypes, they function differently. The DRA sfNK secrete more TNFα and IFNγ upon exposure to IL-2 and IL-15. Consequently, we suggest that sfNK cells may be a marker for more severely destructive RA disease. |
format | Online Article Text |
id | pubmed-6361912 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-63619122019-02-06 High percentages and activity of synovial fluid NK cells present in patients with advanced stage active Rheumatoid Arthritis Yamin, Rachel Berhani, Orit Peleg, Hagit Aamar, Suhail Stein, Natan Gamliel, Moriya Hindi, Issam Scheiman-Elazary, Anat Gur, Chamutal Sci Rep Article Rheumatoid Arthritis (RA) causes chronic inflammation of joints. The cytokines TNFα and IFNγ are central players in RA, however their source has not been fully elucidated. Natural Killer (NK) cells are best known for their role in elimination of viral-infected and transformed cells, and they secrete pro-inflammatory cytokines. NK cells are present in the synovial fluids (SFs) of RA patients and are considered to be important in bone destruction. However, the phenotype and function of NK cells in the SFs of patients with erosive deformative RA (DRA) versus non-deformative RA (NDRA) is poorly characterized. Here we characterize the NK cell populations present in the blood and SFs of DRA and NDRA patients. We demonstrate that a distinct population of activated synovial fluid NK (sfNK) cells constitutes a large proportion of immune cells found in the SFs of DRA patients. We discovered that although sfNK cells in both DRA and NDRA patients have similar phenotypes, they function differently. The DRA sfNK secrete more TNFα and IFNγ upon exposure to IL-2 and IL-15. Consequently, we suggest that sfNK cells may be a marker for more severely destructive RA disease. Nature Publishing Group UK 2019-02-04 /pmc/articles/PMC6361912/ /pubmed/30718650 http://dx.doi.org/10.1038/s41598-018-37448-z Text en © The Author(s) 2019 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Yamin, Rachel Berhani, Orit Peleg, Hagit Aamar, Suhail Stein, Natan Gamliel, Moriya Hindi, Issam Scheiman-Elazary, Anat Gur, Chamutal High percentages and activity of synovial fluid NK cells present in patients with advanced stage active Rheumatoid Arthritis |
title | High percentages and activity of synovial fluid NK cells present in patients with advanced stage active Rheumatoid Arthritis |
title_full | High percentages and activity of synovial fluid NK cells present in patients with advanced stage active Rheumatoid Arthritis |
title_fullStr | High percentages and activity of synovial fluid NK cells present in patients with advanced stage active Rheumatoid Arthritis |
title_full_unstemmed | High percentages and activity of synovial fluid NK cells present in patients with advanced stage active Rheumatoid Arthritis |
title_short | High percentages and activity of synovial fluid NK cells present in patients with advanced stage active Rheumatoid Arthritis |
title_sort | high percentages and activity of synovial fluid nk cells present in patients with advanced stage active rheumatoid arthritis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6361912/ https://www.ncbi.nlm.nih.gov/pubmed/30718650 http://dx.doi.org/10.1038/s41598-018-37448-z |
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