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Evaluation and comparison of adaptive immunity through analyzing the diversities and clonalities of T-cell receptor repertoires in the peripheral blood
The adaptive immune system plays an important role in defending against different kinds of diseases, including infection and cancer. There has been a longtime need for a simple method to quantitatively evaluate the potency of adaptive immunity in our bodies. The tremendously diversified T-cell recep...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9493076/ https://www.ncbi.nlm.nih.gov/pubmed/36159829 http://dx.doi.org/10.3389/fimmu.2022.916430 |
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author | Zhuo, Yue Yang, Xin Shuai, Ping Yang, Liangliang Wen, Xueping Zhong, Xuemei Yang, Shihan Xu, Shaoxian Liu, Yuping Zhang, Zhixin |
author_facet | Zhuo, Yue Yang, Xin Shuai, Ping Yang, Liangliang Wen, Xueping Zhong, Xuemei Yang, Shihan Xu, Shaoxian Liu, Yuping Zhang, Zhixin |
author_sort | Zhuo, Yue |
collection | PubMed |
description | The adaptive immune system plays an important role in defending against different kinds of diseases, including infection and cancer. There has been a longtime need for a simple method to quantitatively evaluate the potency of adaptive immunity in our bodies. The tremendously diversified T-cell receptor (TCR) repertoires are the foundation of the adaptive immune system. In this study, we analyzed the expressed TCRβ repertoires in the peripheral blood of 582 healthy donors and 60 cancer patients. The TCR repertoire in each individual is different, with different usages of TCR Vβ and Jβ genes. Importantly, the TCR diversity and clonality change along with age and disease situation. Most elder individuals and cancer patients have elevated numbers of large TCRβ clones and reduced numbers of shared common clones, and thus, they have very low TCR diversity index (D(50)) values. These results reveal the alteration of the expressed TCRβ repertoire with aging and oncogenesis, and thus, we hypothesize that the TCR diversity and clonality in the peripheral blood might be used to evaluate and compare the adaptive immunities among different individuals in clinical practice. |
format | Online Article Text |
id | pubmed-9493076 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-94930762022-09-23 Evaluation and comparison of adaptive immunity through analyzing the diversities and clonalities of T-cell receptor repertoires in the peripheral blood Zhuo, Yue Yang, Xin Shuai, Ping Yang, Liangliang Wen, Xueping Zhong, Xuemei Yang, Shihan Xu, Shaoxian Liu, Yuping Zhang, Zhixin Front Immunol Immunology The adaptive immune system plays an important role in defending against different kinds of diseases, including infection and cancer. There has been a longtime need for a simple method to quantitatively evaluate the potency of adaptive immunity in our bodies. The tremendously diversified T-cell receptor (TCR) repertoires are the foundation of the adaptive immune system. In this study, we analyzed the expressed TCRβ repertoires in the peripheral blood of 582 healthy donors and 60 cancer patients. The TCR repertoire in each individual is different, with different usages of TCR Vβ and Jβ genes. Importantly, the TCR diversity and clonality change along with age and disease situation. Most elder individuals and cancer patients have elevated numbers of large TCRβ clones and reduced numbers of shared common clones, and thus, they have very low TCR diversity index (D(50)) values. These results reveal the alteration of the expressed TCRβ repertoire with aging and oncogenesis, and thus, we hypothesize that the TCR diversity and clonality in the peripheral blood might be used to evaluate and compare the adaptive immunities among different individuals in clinical practice. Frontiers Media S.A. 2022-09-08 /pmc/articles/PMC9493076/ /pubmed/36159829 http://dx.doi.org/10.3389/fimmu.2022.916430 Text en Copyright © 2022 Zhuo, Yang, Shuai, Yang, Wen, Zhong, Yang, Xu, Liu and Zhang https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Immunology Zhuo, Yue Yang, Xin Shuai, Ping Yang, Liangliang Wen, Xueping Zhong, Xuemei Yang, Shihan Xu, Shaoxian Liu, Yuping Zhang, Zhixin Evaluation and comparison of adaptive immunity through analyzing the diversities and clonalities of T-cell receptor repertoires in the peripheral blood |
title | Evaluation and comparison of adaptive immunity through analyzing the diversities and clonalities of T-cell receptor repertoires in the peripheral blood |
title_full | Evaluation and comparison of adaptive immunity through analyzing the diversities and clonalities of T-cell receptor repertoires in the peripheral blood |
title_fullStr | Evaluation and comparison of adaptive immunity through analyzing the diversities and clonalities of T-cell receptor repertoires in the peripheral blood |
title_full_unstemmed | Evaluation and comparison of adaptive immunity through analyzing the diversities and clonalities of T-cell receptor repertoires in the peripheral blood |
title_short | Evaluation and comparison of adaptive immunity through analyzing the diversities and clonalities of T-cell receptor repertoires in the peripheral blood |
title_sort | evaluation and comparison of adaptive immunity through analyzing the diversities and clonalities of t-cell receptor repertoires in the peripheral blood |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9493076/ https://www.ncbi.nlm.nih.gov/pubmed/36159829 http://dx.doi.org/10.3389/fimmu.2022.916430 |
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