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10.1038/s41590-020-00808-x

http://scihub22266oqcxt.onion/10.1038/s41590-020-00808-x
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32999467!ä!32999467

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suck abstract from ncbi


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pmid32999467      Nat+Immunol 2021 ; 22 (1): 74-85
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  • SARS-CoV-2-derived peptides define heterologous and COVID-19-induced T cell recognition #MMPMID32999467
  • Nelde A; Bilich T; Heitmann JS; Maringer Y; Salih HR; Roerden M; Lubke M; Bauer J; Rieth J; Wacker M; Peter A; Horber S; Traenkle B; Kaiser PD; Rothbauer U; Becker M; Junker D; Krause G; Strengert M; Schneiderhan-Marra N; Templin MF; Joos TO; Kowalewski DJ; Stos-Zweifel V; Fehr M; Rabsteyn A; Mirakaj V; Karbach J; Jager E; Graf M; Gruber LC; Rachfalski D; Preuss B; Hagelstein I; Marklin M; Bakchoul T; Gouttefangeas C; Kohlbacher O; Klein R; Stevanovic S; Rammensee HG; Walz JS
  • Nat Immunol 2021[Jan]; 22 (1): 74-85 PMID32999467show ga
  • T cell immunity is central for the control of viral infections. To characterize T cell immunity, but also for the development of vaccines, identification of exact viral T cell epitopes is fundamental. Here we identify and characterize multiple dominant and subdominant SARS-CoV-2 HLA class I and HLA-DR peptides as potential T cell epitopes in COVID-19 convalescent and unexposed individuals. SARS-CoV-2-specific peptides enabled detection of post-infectious T cell immunity, even in seronegative convalescent individuals. Cross-reactive SARS-CoV-2 peptides revealed pre-existing T cell responses in 81% of unexposed individuals and validated similarity with common cold coronaviruses, providing a functional basis for heterologous immunity in SARS-CoV-2 infection. Diversity of SARS-CoV-2 T cell responses was associated with mild symptoms of COVID-19, providing evidence that immunity requires recognition of multiple epitopes. Together, the proposed SARS-CoV-2 T cell epitopes enable identification of heterologous and post-infectious T cell immunity and facilitate development of diagnostic, preventive and therapeutic measures for COVID-19.
  • |COVID-19/*immunology/prevention & control/virology[MESH]
  • |Cross Reactions/immunology[MESH]
  • |Epitopes, T-Lymphocyte/*immunology[MESH]
  • |HLA-DR Antigens/immunology/metabolism[MESH]
  • |Histocompatibility Antigens Class I/immunology/metabolism[MESH]
  • |Humans[MESH]
  • |Immunologic Memory/immunology[MESH]
  • |Peptides/*immunology[MESH]
  • |SARS-CoV-2/*immunology/physiology[MESH]
  • |T-Lymphocytes/*immunology/metabolism[MESH]


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