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10.1038/s41556-021-00690-1

http://scihub22266oqcxt.onion/10.1038/s41556-021-00690-1
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34108657!9105401!34108657
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suck abstract from ncbi


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pmid34108657      Nat+Cell+Biol 2021 ; 23 (6): 620-630
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  • Single-cell epigenomic landscape of peripheral immune cells reveals establishment of trained immunity in individuals convalescing from COVID-19 #MMPMID34108657
  • You M; Chen L; Zhang D; Zhao P; Chen Z; Qin EQ; Gao Y; Davis MM; Yang P
  • Nat Cell Biol 2021[Jun]; 23 (6): 620-630 PMID34108657show ga
  • Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection often causes severe complications and even death. However, asymptomatic infection has also been reported, highlighting the difference in immune responses among individuals. Here we performed single-cell chromatin accessibility and T cell-receptor analyses of peripheral blood mononuclear cells collected from individuals convalescing from COVID-19 and healthy donors. Chromatin remodelling was observed in both innate and adaptive immune cells in the individuals convalescing from COVID-19. Compared with healthy donors, recovered individuals contained abundant TBET-enriched CD16(+) and IRF1-enriched CD14(+) monocytes with sequential trained and activated epigenomic states. The B-cell lineage in recovered individuals exhibited an accelerated developmental programme from immature B cells to antibody-producing plasma cells. Finally, an integrated analysis of single-cell T cell-receptor clonality with the chromatin accessibility landscape revealed the expansion of putative SARS-CoV-2-specific CD8(+) T cells with epigenomic profiles that promote the differentiation of effector or memory cells. Overall, our data suggest that immune cells of individuals convalescing from COVID-19 exhibit global remodelling of the chromatin accessibility landscape, indicative of the establishment of immunological memory.
  • |*Epigenesis, Genetic[MESH]
  • |*Epigenomics[MESH]
  • |*Genes, T-Cell Receptor[MESH]
  • |*Immunologic Memory[MESH]
  • |*Single-Cell Analysis[MESH]
  • |Adaptive Immunity[MESH]
  • |Adolescent[MESH]
  • |Adult[MESH]
  • |Aged[MESH]
  • |B-Lymphocytes/immunology/metabolism/virology[MESH]
  • |CD8-Positive T-Lymphocytes/immunology/metabolism/virology[MESH]
  • |COVID-19/*genetics/immunology/metabolism/virology[MESH]
  • |Case-Control Studies[MESH]
  • |Cell Differentiation[MESH]
  • |Chromatin Assembly and Disassembly[MESH]
  • |Female[MESH]
  • |Gene Expression Profiling[MESH]
  • |Host-Pathogen Interactions[MESH]
  • |Humans[MESH]
  • |Immunity, Innate[MESH]
  • |Lymphocyte Subsets/*immunology/metabolism/virology[MESH]
  • |Male[MESH]
  • |Middle Aged[MESH]
  • |Monocytes/*immunology/metabolism/virology[MESH]
  • |SARS-CoV-2/*immunology/pathogenicity[MESH]


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