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10.4049/jimmunol.2100131

http://scihub22266oqcxt.onion/10.4049/jimmunol.2100131
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34417260!ä!34417260

suck abstract from ncbi


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pmid34417260      J+Immunol 2021 ; 207 (6): 1591-1598
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  • SARS-CoV-2 Infection Drives a Glycan Switch of Peripheral T Cells at Diagnosis #MMPMID34417260
  • Alves I; Vicente MM; Gaifem J; Fernandes A; Dias AM; Rodrigues CS; Oliveira JC; Seixas N; Malheiro L; Abreu MA; Sarmento E Castro R; Pinho SS
  • J Immunol 2021[Sep]; 207 (6): 1591-1598 PMID34417260show ga
  • COVID-19 is a highly selective disease in which SARS-CoV-2 infection can result in different clinical manifestations ranging from asymptomatic/mild to severe disease that requires hospitalization. In this study, we demonstrated that SARS-CoV-2 infection results in a glycosylation reprogramming of circulating lymphocytes at diagnosis. We identified a specific glycosignature of T cells, defined upon SARS-CoV-2 infection and apparently triggered by a serological factor. This specific glycan switch of T cells is detected at diagnosis being more pronounced in asymptomatic patients. We further demonstrated that asymptomatic patients display an increased expression of a viral-sensing receptor through the upregulation of DC-SIGN in monocytes. We showed that higher levels of DC-SIGN in monocytes at diagnosis correlates with better COVID-19 prognosis. This new evidence pave the way to the identification of a novel glycan-based response in T cells that may confer protection against SARS-CoV-2 infection in asymptomatic patients, highlighting a novel prognostic biomarker and potential therapeutic target.
  • |*COVID-19[MESH]
  • |*SARS-CoV-2[MESH]
  • |Humans[MESH]
  • |Polysaccharides[MESH]
  • |Receptors, Virus[MESH]


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