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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...

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Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Inc. 2021
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
Descripción
Sumario: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.