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Comprehensive analysis of TCR repertoire in COVID-19 using single cell sequencing
T-cell receptor (TCR) is crucial in T cell-mediated virus clearance. To date, TCR bias has been observed in various diseases. However, studies on the TCR repertoire of COVID-19 patients are lacking. Here, we used single-cell V(D)J sequencing to conduct comparative analyses of TCR repertoire between...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7833309/ https://www.ncbi.nlm.nih.gov/pubmed/33383142 http://dx.doi.org/10.1016/j.ygeno.2020.12.036 |
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author | Wang, Pingping Jin, Xiyun Zhou, Wenyang Luo, Meng Xu, Zhaochun Xu, Chang Li, Yiqun Ma, Kexin Cao, Huimin Huang, Yan Xue, Guangfu Jin, Shuilin Nie, Huan Jiang, Qinghua |
author_facet | Wang, Pingping Jin, Xiyun Zhou, Wenyang Luo, Meng Xu, Zhaochun Xu, Chang Li, Yiqun Ma, Kexin Cao, Huimin Huang, Yan Xue, Guangfu Jin, Shuilin Nie, Huan Jiang, Qinghua |
author_sort | Wang, Pingping |
collection | PubMed |
description | T-cell receptor (TCR) is crucial in T cell-mediated virus clearance. To date, TCR bias has been observed in various diseases. However, studies on the TCR repertoire of COVID-19 patients are lacking. Here, we used single-cell V(D)J sequencing to conduct comparative analyses of TCR repertoire between 12 COVID-19 patients and 6 healthy controls, as well as other virus-infected samples. We observed distinct T cell clonal expansion in COVID-19. Further analysis of VJ gene combination revealed 6 VJ pairs significantly increased, while 139 pairs significantly decreased in COVID-19 patients. When considering the VJ combination of α and β chains at the same time, the combination with the highest frequency on COVID-19 was TRAV12-2-J27-TRBV7-9-J2-3. Besides, preferential usage of V and J gene segments was also observed in samples infected by different viruses. Our study provides novel insights on TCR in COVID-19, which contribute to our understanding of the immune response induced by SARS-CoV-2. |
format | Online Article Text |
id | pubmed-7833309 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-78333092021-01-26 Comprehensive analysis of TCR repertoire in COVID-19 using single cell sequencing Wang, Pingping Jin, Xiyun Zhou, Wenyang Luo, Meng Xu, Zhaochun Xu, Chang Li, Yiqun Ma, Kexin Cao, Huimin Huang, Yan Xue, Guangfu Jin, Shuilin Nie, Huan Jiang, Qinghua Genomics Original Article T-cell receptor (TCR) is crucial in T cell-mediated virus clearance. To date, TCR bias has been observed in various diseases. However, studies on the TCR repertoire of COVID-19 patients are lacking. Here, we used single-cell V(D)J sequencing to conduct comparative analyses of TCR repertoire between 12 COVID-19 patients and 6 healthy controls, as well as other virus-infected samples. We observed distinct T cell clonal expansion in COVID-19. Further analysis of VJ gene combination revealed 6 VJ pairs significantly increased, while 139 pairs significantly decreased in COVID-19 patients. When considering the VJ combination of α and β chains at the same time, the combination with the highest frequency on COVID-19 was TRAV12-2-J27-TRBV7-9-J2-3. Besides, preferential usage of V and J gene segments was also observed in samples infected by different viruses. Our study provides novel insights on TCR in COVID-19, which contribute to our understanding of the immune response induced by SARS-CoV-2. Elsevier Inc. 2021-03 2020-12-28 /pmc/articles/PMC7833309/ /pubmed/33383142 http://dx.doi.org/10.1016/j.ygeno.2020.12.036 Text en © 2020 Elsevier Inc. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Original Article Wang, Pingping Jin, Xiyun Zhou, Wenyang Luo, Meng Xu, Zhaochun Xu, Chang Li, Yiqun Ma, Kexin Cao, Huimin Huang, Yan Xue, Guangfu Jin, Shuilin Nie, Huan Jiang, Qinghua Comprehensive analysis of TCR repertoire in COVID-19 using single cell sequencing |
title | Comprehensive analysis of TCR repertoire in COVID-19 using single cell sequencing |
title_full | Comprehensive analysis of TCR repertoire in COVID-19 using single cell sequencing |
title_fullStr | Comprehensive analysis of TCR repertoire in COVID-19 using single cell sequencing |
title_full_unstemmed | Comprehensive analysis of TCR repertoire in COVID-19 using single cell sequencing |
title_short | Comprehensive analysis of TCR repertoire in COVID-19 using single cell sequencing |
title_sort | comprehensive analysis of tcr repertoire in covid-19 using single cell sequencing |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7833309/ https://www.ncbi.nlm.nih.gov/pubmed/33383142 http://dx.doi.org/10.1016/j.ygeno.2020.12.036 |
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