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10.3389/fimmu.2021.635942

http://scihub22266oqcxt.onion/10.3389/fimmu.2021.635942
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suck abstract from ncbi


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pmid34127926      Front+Immunol 2021 ; 12 (ä): 635942
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  • Deconvoluting the T Cell Response to SARS-CoV-2: Specificity Versus Chance and Cognate Cross-Reactivity #MMPMID34127926
  • Lehmann AA; Kirchenbaum GA; Zhang T; Reche PA; Lehmann PV
  • Front Immunol 2021[]; 12 (ä): 635942 PMID34127926show ga
  • SARS-CoV-2 infection takes a mild or clinically inapparent course in the majority of humans who contract this virus. After such individuals have cleared the virus, only the detection of SARS-CoV-2-specific immunological memory can reveal the exposure, and hopefully the establishment of immune protection. With most viral infections, the presence of specific serum antibodies has provided a reliable biomarker for the exposure to the virus of interest. SARS-CoV-2 infection, however, does not reliably induce a durable antibody response, especially in sub-clinically infected individuals. Consequently, it is plausible for a recently infected individual to yield a false negative result within only a few months after exposure. Immunodiagnostic attention has therefore shifted to studies of specific T cell memory to SARS-CoV-2. Most reports published so far agree that a T cell response is engaged during SARS-CoV-2 infection, but they also state that in 20-81% of SARS-CoV-2-unexposed individuals, T cells respond to SARS-CoV-2 antigens (mega peptide pools), allegedly due to T cell cross-reactivity with Common Cold coronaviruses (CCC), or other antigens. Here we show that, by introducing irrelevant mega peptide pools as negative controls to account for chance cross-reactivity, and by establishing the antigen dose-response characteristic of the T cells, one can clearly discern between cognate T cell memory induced by SARS-CoV-2 infection vs. cross-reactive T cell responses in individuals who have not been infected with SARS-CoV-2.
  • |Antigens, Viral/immunology[MESH]
  • |Biomarkers[MESH]
  • |COVID-19/*immunology/metabolism/*virology[MESH]
  • |Cross Reactions/immunology[MESH]
  • |Cytokines/metabolism[MESH]
  • |Epitopes, T-Lymphocyte/immunology[MESH]
  • |Host-Pathogen Interactions/*immunology[MESH]
  • |Humans[MESH]
  • |Immunodominant Epitopes/immunology[MESH]
  • |Immunologic Memory[MESH]
  • |Peptides/immunology[MESH]
  • |Protein Binding[MESH]
  • |SARS-CoV-2/*immunology[MESH]
  • |Spike Glycoprotein, Coronavirus/immunology[MESH]


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