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Immune repertoire analysis of normal Chinese donors at different ages

OBJECTIVES: This study investigated the characteristics of the immune repertoire in normal Chinese individuals of different ages. MATERIALS AND METHODS: In this study, all seven receptor chains from both B and T cells in peripheral blood of 16 normal Chinese individuals from two age groups were anal...

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Autores principales: Song, Cailing, Pan, Wenjing, Brown, Brittany, Tang, Congli, Huang, Yunqi, Chen, Houao, Peng, Nan, Wang, Zhe, Weber, Daniel, Byrne‐Steele, Miranda, Wu, Haijing, Liu, Hongna, Deng, Yan, He, Nongyue, Li, Song
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9628227/
https://www.ncbi.nlm.nih.gov/pubmed/35929064
http://dx.doi.org/10.1111/cpr.13311
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author Song, Cailing
Pan, Wenjing
Brown, Brittany
Tang, Congli
Huang, Yunqi
Chen, Houao
Peng, Nan
Wang, Zhe
Weber, Daniel
Byrne‐Steele, Miranda
Wu, Haijing
Liu, Hongna
Deng, Yan
He, Nongyue
Li, Song
author_facet Song, Cailing
Pan, Wenjing
Brown, Brittany
Tang, Congli
Huang, Yunqi
Chen, Houao
Peng, Nan
Wang, Zhe
Weber, Daniel
Byrne‐Steele, Miranda
Wu, Haijing
Liu, Hongna
Deng, Yan
He, Nongyue
Li, Song
author_sort Song, Cailing
collection PubMed
description OBJECTIVES: This study investigated the characteristics of the immune repertoire in normal Chinese individuals of different ages. MATERIALS AND METHODS: In this study, all seven receptor chains from both B and T cells in peripheral blood of 16 normal Chinese individuals from two age groups were analyzed using high‐throughput sequencing and dimer‐avoided multiplex PCR amplification. Normal in this study is defined as no chronic, infectious or autoimmune disease within 6 months prior to blood draw. RESULTS: We found that compared with the younger group, the clonal expression of T‐cell receptor repertoire increased in the older group, while diversity decreased. In addition, we found that the T‐cell receptor repertoire was more significantly affected by age than the B‐cell receptor repertoire, including significant differences in the use of the unique TCR‐alpha and TCR‐beta V‐J gene combinations, in the two groups of normal participants. We further analyzed the degree of complementarity determining region 3 sequence sharing between the two groups, and found shared TCR‐alpha, TCR‐gamma, immunoglobulin‐kappa and immunoglobulin‐lambda chain complementarity determining region 3 sequences in all subjects. CONCLUSION: Taken together, our study gives us a better understanding of the immune repertoire of different normal Chinese people, and these results can be applied to the treatment of age‐related diseases. Immune repertoire analysis also allows us to observe participant's wellness, aiding in early‐stage diagnosis.
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spelling pubmed-96282272022-11-03 Immune repertoire analysis of normal Chinese donors at different ages Song, Cailing Pan, Wenjing Brown, Brittany Tang, Congli Huang, Yunqi Chen, Houao Peng, Nan Wang, Zhe Weber, Daniel Byrne‐Steele, Miranda Wu, Haijing Liu, Hongna Deng, Yan He, Nongyue Li, Song Cell Prolif Original Articles OBJECTIVES: This study investigated the characteristics of the immune repertoire in normal Chinese individuals of different ages. MATERIALS AND METHODS: In this study, all seven receptor chains from both B and T cells in peripheral blood of 16 normal Chinese individuals from two age groups were analyzed using high‐throughput sequencing and dimer‐avoided multiplex PCR amplification. Normal in this study is defined as no chronic, infectious or autoimmune disease within 6 months prior to blood draw. RESULTS: We found that compared with the younger group, the clonal expression of T‐cell receptor repertoire increased in the older group, while diversity decreased. In addition, we found that the T‐cell receptor repertoire was more significantly affected by age than the B‐cell receptor repertoire, including significant differences in the use of the unique TCR‐alpha and TCR‐beta V‐J gene combinations, in the two groups of normal participants. We further analyzed the degree of complementarity determining region 3 sequence sharing between the two groups, and found shared TCR‐alpha, TCR‐gamma, immunoglobulin‐kappa and immunoglobulin‐lambda chain complementarity determining region 3 sequences in all subjects. CONCLUSION: Taken together, our study gives us a better understanding of the immune repertoire of different normal Chinese people, and these results can be applied to the treatment of age‐related diseases. Immune repertoire analysis also allows us to observe participant's wellness, aiding in early‐stage diagnosis. John Wiley and Sons Inc. 2022-08-04 /pmc/articles/PMC9628227/ /pubmed/35929064 http://dx.doi.org/10.1111/cpr.13311 Text en © 2022 The Authors. Cell Proliferation published by Beijing Institute for Stem Cell and Regenerative Medicine and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Song, Cailing
Pan, Wenjing
Brown, Brittany
Tang, Congli
Huang, Yunqi
Chen, Houao
Peng, Nan
Wang, Zhe
Weber, Daniel
Byrne‐Steele, Miranda
Wu, Haijing
Liu, Hongna
Deng, Yan
He, Nongyue
Li, Song
Immune repertoire analysis of normal Chinese donors at different ages
title Immune repertoire analysis of normal Chinese donors at different ages
title_full Immune repertoire analysis of normal Chinese donors at different ages
title_fullStr Immune repertoire analysis of normal Chinese donors at different ages
title_full_unstemmed Immune repertoire analysis of normal Chinese donors at different ages
title_short Immune repertoire analysis of normal Chinese donors at different ages
title_sort immune repertoire analysis of normal chinese donors at different ages
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9628227/
https://www.ncbi.nlm.nih.gov/pubmed/35929064
http://dx.doi.org/10.1111/cpr.13311
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