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10.1371/journal.ppat.1009766

http://scihub22266oqcxt.onion/10.1371/journal.ppat.1009766
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34280244!8321400!34280244
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suck abstract from ncbi


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pmid34280244      PLoS+Pathog 2021 ; 17 (7): e1009766
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  • Early antibody responses associated with survival in COVID19 patients #MMPMID34280244
  • Zhou ZH; Dharmarajan S; Lehtimaki M; Kirshner SL; Kozlowski S
  • PLoS Pathog 2021[Jul]; 17 (7): e1009766 PMID34280244show ga
  • Neutralizing antibodies to the SARS CoV-2 spike proteins have been issued Emergency Use Authorizations and are a likely mechanism of vaccines to prevent COVID-19. However, benefit of treatment with monoclonal antibodies has only been observed in clinical trials in outpatients with mild to moderate COVID-19 but not in patients who are hospitalized and/or have advanced disease. To address this observation, we evaluated the timing of anti SARS-CoV-2 antibody production in hospitalized patients with the use of a highly sensitive multiplexed bead-based immunoassay allowing for early detection of antibodies to SARS-CoV-2. We found significantly lower levels of antibodies to the SARS-CoV-2 spike protein in the first week after symptom onset in patients who expired as compared to patients who were discharged. We also developed a model to characterize the relationship between each patient's individual antibody level trajectory and eventual COVID 19 outcome which can be adapted into a prediction model with more data.
  • |Adult[MESH]
  • |Aged[MESH]
  • |Aged, 80 and over[MESH]
  • |Antibodies, Viral/*blood[MESH]
  • |Antibody Specificity[MESH]
  • |Antigens, Viral/immunology[MESH]
  • |COVID-19/*immunology/*mortality[MESH]
  • |Female[MESH]
  • |Humans[MESH]
  • |Immunoglobulin G/blood[MESH]
  • |Linear Models[MESH]
  • |Male[MESH]
  • |Middle Aged[MESH]
  • |Models, Immunological[MESH]
  • |Pandemics[MESH]
  • |Prognosis[MESH]
  • |SARS-CoV-2/*immunology[MESH]
  • |Spike Glycoprotein, Coronavirus/immunology[MESH]
  • |Time Factors[MESH]


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