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Characteristic patterns of HLA presentation and T cell differentiation in adult-onset Still’s disease

We examined the expression of human leukocyte antigen (HLA) and composition of differentiated T cells in the peripheral blood to understand the characteristics of the immune changes in patients with adult-onset Still’s disease (AOSD). This study enrolled patients with AOSD (n = 14), patients with rh...

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Autores principales: Jung, Ju-Yang, Choi, Bunsoon, Sayeed, Hasan MD, Suh, Chang-Hee, Kim, Ye Won, Kim, Hyoun-Ah, Sohn, Seonghyang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6073833/
https://www.ncbi.nlm.nih.gov/pubmed/30052100
http://dx.doi.org/10.1177/2058738418791284
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author Jung, Ju-Yang
Choi, Bunsoon
Sayeed, Hasan MD
Suh, Chang-Hee
Kim, Ye Won
Kim, Hyoun-Ah
Sohn, Seonghyang
author_facet Jung, Ju-Yang
Choi, Bunsoon
Sayeed, Hasan MD
Suh, Chang-Hee
Kim, Ye Won
Kim, Hyoun-Ah
Sohn, Seonghyang
author_sort Jung, Ju-Yang
collection PubMed
description We examined the expression of human leukocyte antigen (HLA) and composition of differentiated T cells in the peripheral blood to understand the characteristics of the immune changes in patients with adult-onset Still’s disease (AOSD). This study enrolled patients with AOSD (n = 14), patients with rheumatoid arthritis (RA, n = 20), and healthy controls (HC, n = 20). The percentage of surface-stained cells with HLA-DP, DQ, and DR alleles and the composition of differentiated T cells in peripheral blood leukocytes (PBLs) were evaluated by flow cytometry. AOSD patients exhibited significantly higher percentages of lymphocytes presenting HLA-DP and HLA-DR, and lower percentages of cells presenting HLA-DQ, than RA patients or HC. The proportions of CD4+, CD4+CCR7+, CD4+CD62L–, and CD8+CD62L– cells from PBLs were decreased in AOSD patients relative to RA patients or HCs. By contrast, AOSD patients had higher proportions of CD8+naïve T cells in whole blood relative to RA patients or HC. The proportions of CD4+ effector memory T cells, CD8+ naïve T cells, and CD8+ effector memory T cells in whole blood cells and CD4+ effector memory T cell in lymphocytes were significantly associated with the systemic score. While the proportions of CD4+, CD8+, CCR7+, CD4+CCR7+, CD4+CD62L–, and CD8+CD62L– cells were significantly decreased in AOSD patients, and the proportion of CD8+naïve T cells was elevated in AOSD and correlated with the systemic score. Further studies of a large cohort of AOSD patients will be necessary to evaluate these markers in the pathogenesis of AOSD.
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spelling pubmed-60738332018-08-06 Characteristic patterns of HLA presentation and T cell differentiation in adult-onset Still’s disease Jung, Ju-Yang Choi, Bunsoon Sayeed, Hasan MD Suh, Chang-Hee Kim, Ye Won Kim, Hyoun-Ah Sohn, Seonghyang Int J Immunopathol Pharmacol Letter to the Editor We examined the expression of human leukocyte antigen (HLA) and composition of differentiated T cells in the peripheral blood to understand the characteristics of the immune changes in patients with adult-onset Still’s disease (AOSD). This study enrolled patients with AOSD (n = 14), patients with rheumatoid arthritis (RA, n = 20), and healthy controls (HC, n = 20). The percentage of surface-stained cells with HLA-DP, DQ, and DR alleles and the composition of differentiated T cells in peripheral blood leukocytes (PBLs) were evaluated by flow cytometry. AOSD patients exhibited significantly higher percentages of lymphocytes presenting HLA-DP and HLA-DR, and lower percentages of cells presenting HLA-DQ, than RA patients or HC. The proportions of CD4+, CD4+CCR7+, CD4+CD62L–, and CD8+CD62L– cells from PBLs were decreased in AOSD patients relative to RA patients or HCs. By contrast, AOSD patients had higher proportions of CD8+naïve T cells in whole blood relative to RA patients or HC. The proportions of CD4+ effector memory T cells, CD8+ naïve T cells, and CD8+ effector memory T cells in whole blood cells and CD4+ effector memory T cell in lymphocytes were significantly associated with the systemic score. While the proportions of CD4+, CD8+, CCR7+, CD4+CCR7+, CD4+CD62L–, and CD8+CD62L– cells were significantly decreased in AOSD patients, and the proportion of CD8+naïve T cells was elevated in AOSD and correlated with the systemic score. Further studies of a large cohort of AOSD patients will be necessary to evaluate these markers in the pathogenesis of AOSD. SAGE Publications 2018-07-27 /pmc/articles/PMC6073833/ /pubmed/30052100 http://dx.doi.org/10.1177/2058738418791284 Text en © The Author(s) 2018 http://www.creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Letter to the Editor
Jung, Ju-Yang
Choi, Bunsoon
Sayeed, Hasan MD
Suh, Chang-Hee
Kim, Ye Won
Kim, Hyoun-Ah
Sohn, Seonghyang
Characteristic patterns of HLA presentation and T cell differentiation in adult-onset Still’s disease
title Characteristic patterns of HLA presentation and T cell differentiation in adult-onset Still’s disease
title_full Characteristic patterns of HLA presentation and T cell differentiation in adult-onset Still’s disease
title_fullStr Characteristic patterns of HLA presentation and T cell differentiation in adult-onset Still’s disease
title_full_unstemmed Characteristic patterns of HLA presentation and T cell differentiation in adult-onset Still’s disease
title_short Characteristic patterns of HLA presentation and T cell differentiation in adult-onset Still’s disease
title_sort characteristic patterns of hla presentation and t cell differentiation in adult-onset still’s disease
topic Letter to the Editor
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6073833/
https://www.ncbi.nlm.nih.gov/pubmed/30052100
http://dx.doi.org/10.1177/2058738418791284
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