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Correlation between Peripheral T Cell Subsets and the Activity of Thyroid-Associated Ophthalmopathy
INTRODUCTION: Thyroid-associated ophthalmopathy (TAO) is the most common orbital immunological disease in adults. T cells play an important role in the pathogenesis of TAO. However, our knowledge of the circulating T cell subsets in TAO is limited. OBJECTIVE: To investigate the circulating T cell su...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8924605/ https://www.ncbi.nlm.nih.gov/pubmed/35311030 http://dx.doi.org/10.1155/2022/2705650 |
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author | Hu, Hong Liang, Liang Ge, Qian Jiang, Xing Fu, Zhizheng Liu, Chun Long, Jian |
author_facet | Hu, Hong Liang, Liang Ge, Qian Jiang, Xing Fu, Zhizheng Liu, Chun Long, Jian |
author_sort | Hu, Hong |
collection | PubMed |
description | INTRODUCTION: Thyroid-associated ophthalmopathy (TAO) is the most common orbital immunological disease in adults. T cells play an important role in the pathogenesis of TAO. However, our knowledge of the circulating T cell subsets in TAO is limited. OBJECTIVE: To investigate the circulating T cell subsets in TAO and the correlations between them and the activity of TAO. METHODS: Thirty-eight TAO patients (19 active and 19 nonactive) were enrolled. The absolute number and percentage of total lymphocytes, CD3+T cells, CD4+T cells, CD8+ T cells, CD3+CD4-CD8-T cells (DNT cells), and CD3+CD4+CD8+ T cells (DPT cells) in peripheral blood were measured by flow cytometer. RESULTS: TAO patients were divided into the active group and the nonactive group by the clinical activity score (CAS). The mean CAS was 4 ± 1.11 in the active group and 1.47 ± 0.61 in the nonactive group. No statistical differences were found in gender, age, and the levels of FT3, FT4, TSH, and TRAb between the two groups. The percentage of DNT cells was lower in the active group than in the non-active group, and it was negatively correlated with CAS (r = −0.349, P=0.032), but not the absolute number. The CD4/CD8 ratio, the absolute number and percentage of CD3+ T cells, CD4+ T cells, CD8+ T cells, and DPT cells did not differ between the two groups. CONCLUSION: In the present study, we found the percentage of DNT cells was significantly lesser in the active TAO than in the nonactive TAO, and it was negatively correlated with the activity of the TAO. It suggests that DNT cells may involve in the immunopathogenesis of TAO and can serve as a clinical biomarker of the disease activity. |
format | Online Article Text |
id | pubmed-8924605 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-89246052022-03-17 Correlation between Peripheral T Cell Subsets and the Activity of Thyroid-Associated Ophthalmopathy Hu, Hong Liang, Liang Ge, Qian Jiang, Xing Fu, Zhizheng Liu, Chun Long, Jian Int J Endocrinol Research Article INTRODUCTION: Thyroid-associated ophthalmopathy (TAO) is the most common orbital immunological disease in adults. T cells play an important role in the pathogenesis of TAO. However, our knowledge of the circulating T cell subsets in TAO is limited. OBJECTIVE: To investigate the circulating T cell subsets in TAO and the correlations between them and the activity of TAO. METHODS: Thirty-eight TAO patients (19 active and 19 nonactive) were enrolled. The absolute number and percentage of total lymphocytes, CD3+T cells, CD4+T cells, CD8+ T cells, CD3+CD4-CD8-T cells (DNT cells), and CD3+CD4+CD8+ T cells (DPT cells) in peripheral blood were measured by flow cytometer. RESULTS: TAO patients were divided into the active group and the nonactive group by the clinical activity score (CAS). The mean CAS was 4 ± 1.11 in the active group and 1.47 ± 0.61 in the nonactive group. No statistical differences were found in gender, age, and the levels of FT3, FT4, TSH, and TRAb between the two groups. The percentage of DNT cells was lower in the active group than in the non-active group, and it was negatively correlated with CAS (r = −0.349, P=0.032), but not the absolute number. The CD4/CD8 ratio, the absolute number and percentage of CD3+ T cells, CD4+ T cells, CD8+ T cells, and DPT cells did not differ between the two groups. CONCLUSION: In the present study, we found the percentage of DNT cells was significantly lesser in the active TAO than in the nonactive TAO, and it was negatively correlated with the activity of the TAO. It suggests that DNT cells may involve in the immunopathogenesis of TAO and can serve as a clinical biomarker of the disease activity. Hindawi 2022-03-08 /pmc/articles/PMC8924605/ /pubmed/35311030 http://dx.doi.org/10.1155/2022/2705650 Text en Copyright © 2022 Hong Hu et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Hu, Hong Liang, Liang Ge, Qian Jiang, Xing Fu, Zhizheng Liu, Chun Long, Jian Correlation between Peripheral T Cell Subsets and the Activity of Thyroid-Associated Ophthalmopathy |
title | Correlation between Peripheral T Cell Subsets and the Activity of Thyroid-Associated Ophthalmopathy |
title_full | Correlation between Peripheral T Cell Subsets and the Activity of Thyroid-Associated Ophthalmopathy |
title_fullStr | Correlation between Peripheral T Cell Subsets and the Activity of Thyroid-Associated Ophthalmopathy |
title_full_unstemmed | Correlation between Peripheral T Cell Subsets and the Activity of Thyroid-Associated Ophthalmopathy |
title_short | Correlation between Peripheral T Cell Subsets and the Activity of Thyroid-Associated Ophthalmopathy |
title_sort | correlation between peripheral t cell subsets and the activity of thyroid-associated ophthalmopathy |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8924605/ https://www.ncbi.nlm.nih.gov/pubmed/35311030 http://dx.doi.org/10.1155/2022/2705650 |
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