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Immunology repertoire study of pulmonary sarcoidosis T cells in CD4+, CD8+ PBMC and tissue
Sarcoidosis is a systemic granulomatous disorder highly related with immune response. The diversity and stability of the immune system could be measured by hypervariable complementarity-determining region 3 (CDR3) segments of the T cell receptor (TCR). Here we used a combination of multiplex PCR and...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5685688/ https://www.ncbi.nlm.nih.gov/pubmed/29163767 http://dx.doi.org/10.18632/oncotarget.20085 |
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author | Fu, Yingyun Li, Yazhen Xu, Lan Liu, Shengguo Wang, Minlian Xiao, Lu Liu, Song Dai, Yong |
author_facet | Fu, Yingyun Li, Yazhen Xu, Lan Liu, Shengguo Wang, Minlian Xiao, Lu Liu, Song Dai, Yong |
author_sort | Fu, Yingyun |
collection | PubMed |
description | Sarcoidosis is a systemic granulomatous disorder highly related with immune response. The diversity and stability of the immune system could be measured by hypervariable complementarity-determining region 3 (CDR3) segments of the T cell receptor (TCR). Here we used a combination of multiplex PCR and next-generation sequencing to conduct a good quality analysis of the T-cell receptor BV complementarity-determining region 3 (TCR BV CDR3) gene in peripheral blood mononuclear cells (PBMCs) from 7 sarcoidosis patients and lung sarcoidosis tissue from 6 patients. The length distribution of CDR3 sequences identified a significant difference among CD4+, CD8+ and tissue samples. The analysis of Gini coefficient, Shannon entropy and HEC number showed that they all presents in sarcoidosis tissue group clones in a more skewed manner than that of in PMBCs groups. 2 nucleotide sequences and 2 amino acid sequences were shared by all samples. The comparison of TRBV, TRBJ usage and VJ combination frequency identified 2 TRBV genes, 2 TRBJ genes differentially expressed among different groups and different higher usage and lower usage of V-J combinations between each group. |
format | Online Article Text |
id | pubmed-5685688 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-56856882017-11-21 Immunology repertoire study of pulmonary sarcoidosis T cells in CD4+, CD8+ PBMC and tissue Fu, Yingyun Li, Yazhen Xu, Lan Liu, Shengguo Wang, Minlian Xiao, Lu Liu, Song Dai, Yong Oncotarget Research Paper: Immunology Sarcoidosis is a systemic granulomatous disorder highly related with immune response. The diversity and stability of the immune system could be measured by hypervariable complementarity-determining region 3 (CDR3) segments of the T cell receptor (TCR). Here we used a combination of multiplex PCR and next-generation sequencing to conduct a good quality analysis of the T-cell receptor BV complementarity-determining region 3 (TCR BV CDR3) gene in peripheral blood mononuclear cells (PBMCs) from 7 sarcoidosis patients and lung sarcoidosis tissue from 6 patients. The length distribution of CDR3 sequences identified a significant difference among CD4+, CD8+ and tissue samples. The analysis of Gini coefficient, Shannon entropy and HEC number showed that they all presents in sarcoidosis tissue group clones in a more skewed manner than that of in PMBCs groups. 2 nucleotide sequences and 2 amino acid sequences were shared by all samples. The comparison of TRBV, TRBJ usage and VJ combination frequency identified 2 TRBV genes, 2 TRBJ genes differentially expressed among different groups and different higher usage and lower usage of V-J combinations between each group. Impact Journals LLC 2017-08-09 /pmc/articles/PMC5685688/ /pubmed/29163767 http://dx.doi.org/10.18632/oncotarget.20085 Text en Copyright: © 2017 Fu et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License 3.0 (http://creativecommons.org/licenses/by/3.0/) (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper: Immunology Fu, Yingyun Li, Yazhen Xu, Lan Liu, Shengguo Wang, Minlian Xiao, Lu Liu, Song Dai, Yong Immunology repertoire study of pulmonary sarcoidosis T cells in CD4+, CD8+ PBMC and tissue |
title | Immunology repertoire study of pulmonary sarcoidosis T cells in CD4+, CD8+ PBMC and tissue |
title_full | Immunology repertoire study of pulmonary sarcoidosis T cells in CD4+, CD8+ PBMC and tissue |
title_fullStr | Immunology repertoire study of pulmonary sarcoidosis T cells in CD4+, CD8+ PBMC and tissue |
title_full_unstemmed | Immunology repertoire study of pulmonary sarcoidosis T cells in CD4+, CD8+ PBMC and tissue |
title_short | Immunology repertoire study of pulmonary sarcoidosis T cells in CD4+, CD8+ PBMC and tissue |
title_sort | immunology repertoire study of pulmonary sarcoidosis t cells in cd4+, cd8+ pbmc and tissue |
topic | Research Paper: Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5685688/ https://www.ncbi.nlm.nih.gov/pubmed/29163767 http://dx.doi.org/10.18632/oncotarget.20085 |
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