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10.1038/s41392-020-00457-4

http://scihub22266oqcxt.onion/10.1038/s41392-020-00457-4
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33361761!7758413!33361761
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suck abstract from ncbi


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pmid33361761      Signal+Transduct+Target+Ther 2020 ; 5 (1): 294
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  • Longitudinal transcriptome analyses show robust T cell immunity during recovery from COVID-19 #MMPMID33361761
  • Zheng HY; Xu M; Yang CX; Tian RR; Zhang M; Li JJ; Wang XC; Ding ZL; Li GM; Li XL; He YQ; Dong XQ; Yao YG; Zheng YT
  • Signal Transduct Target Ther 2020[Dec]; 5 (1): 294 PMID33361761show ga
  • Understanding the processes of immune regulation in patients infected with the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is crucial for improving treatment. Here, we performed longitudinal whole-transcriptome RNA sequencing on peripheral blood mononuclear cell (PBMC) samples from 18 patients with coronavirus disease 2019 (COVID-19) during their treatment, convalescence, and rehabilitation. After analyzing the regulatory networks of differentially expressed messenger RNAs (mRNAs), microRNAs (miRNAs) and long non-coding RNAs (lncRNAs) between the different clinical stages, we found that humoral immunity and type I interferon response were significantly downregulated, while robust T-cell activation and differentiation at the whole transcriptome level constituted the main events that occurred during recovery from COVID-19. The formation of this T cell immune response might be driven by the activation of activating protein-1 (AP-1) related signaling pathway and was weakly affected by other clinical features. These findings uncovered the dynamic pattern of immune responses and indicated the key role of T cell immunity in the creation of immune protection against this disease.
  • |COVID-19/epidemiology/*genetics/pathology[MESH]
  • |Female[MESH]
  • |Humans[MESH]
  • |Immunity, Humoral/*genetics/immunology[MESH]
  • |Leukocytes, Mononuclear/metabolism[MESH]
  • |Male[MESH]
  • |MicroRNAs[MESH]
  • |RNA, Long Noncoding/genetics[MESH]
  • |RNA-Seq[MESH]
  • |SARS-CoV-2/genetics/pathogenicity[MESH]
  • |T-Lymphocytes/immunology/*metabolism/pathology[MESH]
  • |Transcription Factor AP-1/genetics[MESH]


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