Role of IgG against N-protein of SARS-CoV2 in COVID19 clinical outcomes
The Nucleocapsid Protein (N Protein) of severe acute respiratory syndrome Coronavirus 2 (SARS-CoV2) is located in the viral core. Immunoglobulin G (IgG) targeting N protein is detectable in the serum of infected patients. The effect of high titers of IgG against N-protein on clinical outcomes of SAR...
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| Published in: | Scientific reports Vol. 11; no. 1; pp. 3455 - 9 |
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| Main Authors: | , , , , , , , , , , , , , , , , , , , |
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| Language: | English |
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Nature Publishing Group UK
10.02.2021
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| ISSN: | 2045-2322, 2045-2322 |
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| Abstract | The Nucleocapsid Protein (N Protein) of severe acute respiratory syndrome Coronavirus 2 (SARS-CoV2) is located in the viral core. Immunoglobulin G (IgG) targeting N protein is detectable in the serum of infected patients. The effect of high titers of IgG against N-protein on clinical outcomes of SARS-CoV2 disease has not been described. We studied 400 RT-PCR confirmed SARS-CoV2 patients to determine independent factors associated with poor outcomes, including Medical Intensive Care Unit (MICU) admission, prolonged MICU stay and hospital admissions, and in-hospital mortality. We also measured serum IgG against the N protein and correlated its concentrations with clinical outcomes. We found that several factors, including Charlson comorbidity Index (CCI), high levels of IL6, and presentation with dyspnea were associated with poor clinical outcomes. It was shown that higher CCI and higher IL6 levels were independently associated with in-hospital mortality. Anti-N protein IgG was detected in the serum of 55 (55%) patients at the time of admission. A high concentration of antibodies, defined as signal to cut off ratio (S/Co) > 1.5 (75 percentile of all measurements), was found in 25 (25%) patients. The multivariable logistic regression models showed that between being an African American, higher CCI, lymphocyte counts, and S/Co ratio > 1.5, only S/Co ratio were independently associated with MICU admission and longer length of stay in hospital. This study recommends that titers of IgG targeting N-protein of SARS-CoV2 at admission is a prognostic factor for the clinical course of disease and should be measured in all patients with SARS-CoV2 infection. |
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| AbstractList | The Nucleocapsid Protein (N Protein) of severe acute respiratory syndrome Coronavirus 2 (SARS-CoV2) is located in the viral core. Immunoglobulin G (IgG) targeting N protein is detectable in the serum of infected patients. The effect of high titers of IgG against N-protein on clinical outcomes of SARS-CoV2 disease has not been described. We studied 400 RT-PCR confirmed SARS-CoV2 patients to determine independent factors associated with poor outcomes, including Medical Intensive Care Unit (MICU) admission, prolonged MICU stay and hospital admissions, and in-hospital mortality. We also measured serum IgG against the N protein and correlated its concentrations with clinical outcomes. We found that several factors, including Charlson comorbidity Index (CCI), high levels of IL6, and presentation with dyspnea were associated with poor clinical outcomes. It was shown that higher CCI and higher IL6 levels were independently associated with in-hospital mortality. Anti-N protein IgG was detected in the serum of 55 (55%) patients at the time of admission. A high concentration of antibodies, defined as signal to cut off ratio (S/Co) > 1.5 (75 percentile of all measurements), was found in 25 (25%) patients. The multivariable logistic regression models showed that between being an African American, higher CCI, lymphocyte counts, and S/Co ratio > 1.5, only S/Co ratio were independently associated with MICU admission and longer length of stay in hospital. This study recommends that titers of IgG targeting N-protein of SARS-CoV2 at admission is a prognostic factor for the clinical course of disease and should be measured in all patients with SARS-CoV2 infection. Abstract The Nucleocapsid Protein (N Protein) of severe acute respiratory syndrome Coronavirus 2 (SARS-CoV2) is located in the viral core. Immunoglobulin G (IgG) targeting N protein is detectable in the serum of infected patients. The effect of high titers of IgG against N-protein on clinical outcomes of SARS-CoV2 disease has not been described. We studied 400 RT-PCR confirmed SARS-CoV2 patients to determine independent factors associated with poor outcomes, including Medical Intensive Care Unit (MICU) admission, prolonged MICU stay and hospital admissions, and in-hospital mortality. We also measured serum IgG against the N protein and correlated its concentrations with clinical outcomes. We found that several factors, including Charlson comorbidity Index (CCI), high levels of IL6, and presentation with dyspnea were associated with poor clinical outcomes. It was shown that higher CCI and higher IL6 levels were independently associated with in-hospital mortality. Anti-N protein IgG was detected in the serum of 55 (55%) patients at the time of admission. A high concentration of antibodies, defined as signal to cut off ratio (S/Co) > 1.5 (75 percentile of all measurements), was found in 25 (25%) patients. The multivariable logistic regression models showed that between being an African American, higher CCI, lymphocyte counts, and S/Co ratio > 1.5, only S/Co ratio were independently associated with MICU admission and longer length of stay in hospital. This study recommends that titers of IgG targeting N-protein of SARS-CoV2 at admission is a prognostic factor for the clinical course of disease and should be measured in all patients with SARS-CoV2 infection. The Nucleocapsid Protein (N Protein) of severe acute respiratory syndrome Coronavirus 2 (SARS-CoV2) is located in the viral core. Immunoglobulin G (IgG) targeting N protein is detectable in the serum of infected patients. The effect of high titers of IgG against N-protein on clinical outcomes of SARS-CoV2 disease has not been described. We studied 400 RT-PCR confirmed SARS-CoV2 patients to determine independent factors associated with poor outcomes, including Medical Intensive Care Unit (MICU) admission, prolonged MICU stay and hospital admissions, and in-hospital mortality. We also measured serum IgG against the N protein and correlated its concentrations with clinical outcomes. We found that several factors, including Charlson comorbidity Index (CCI), high levels of IL6, and presentation with dyspnea were associated with poor clinical outcomes. It was shown that higher CCI and higher IL6 levels were independently associated with in-hospital mortality. Anti-N protein IgG was detected in the serum of 55 (55%) patients at the time of admission. A high concentration of antibodies, defined as signal to cut off ratio (S/Co) > 1.5 (75 percentile of all measurements), was found in 25 (25%) patients. The multivariable logistic regression models showed that between being an African American, higher CCI, lymphocyte counts, and S/Co ratio > 1.5, only S/Co ratio were independently associated with MICU admission and longer length of stay in hospital. This study recommends that titers of IgG targeting N-protein of SARS-CoV2 at admission is a prognostic factor for the clinical course of disease and should be measured in all patients with SARS-CoV2 infection.The Nucleocapsid Protein (N Protein) of severe acute respiratory syndrome Coronavirus 2 (SARS-CoV2) is located in the viral core. Immunoglobulin G (IgG) targeting N protein is detectable in the serum of infected patients. The effect of high titers of IgG against N-protein on clinical outcomes of SARS-CoV2 disease has not been described. We studied 400 RT-PCR confirmed SARS-CoV2 patients to determine independent factors associated with poor outcomes, including Medical Intensive Care Unit (MICU) admission, prolonged MICU stay and hospital admissions, and in-hospital mortality. We also measured serum IgG against the N protein and correlated its concentrations with clinical outcomes. We found that several factors, including Charlson comorbidity Index (CCI), high levels of IL6, and presentation with dyspnea were associated with poor clinical outcomes. It was shown that higher CCI and higher IL6 levels were independently associated with in-hospital mortality. Anti-N protein IgG was detected in the serum of 55 (55%) patients at the time of admission. A high concentration of antibodies, defined as signal to cut off ratio (S/Co) > 1.5 (75 percentile of all measurements), was found in 25 (25%) patients. The multivariable logistic regression models showed that between being an African American, higher CCI, lymphocyte counts, and S/Co ratio > 1.5, only S/Co ratio were independently associated with MICU admission and longer length of stay in hospital. This study recommends that titers of IgG targeting N-protein of SARS-CoV2 at admission is a prognostic factor for the clinical course of disease and should be measured in all patients with SARS-CoV2 infection. |
| ArticleNumber | 3455 |
| Author | Clarence, Emile Zhang, Chongxu Bastidas, Maria Virginia Perez Sacher, Camila Sofia Patel, Sayari Mirsaeidi, Mehdi Modarresi, Farzaneh Faghihi, Mohammad Murthi, Mukunthan Santos, Kayo H. M. De La Fuente, Justin Rafa O. Miranda, Justin Nestor Gonzalez, Miguel Santiago Kambali, Shweta Asif, Huda Batra, Mayank Tian, Runxia Mathew, Megan Haddadi, Sara Green, Desmond |
| Author_xml | – sequence: 1 givenname: Mayank surname: Batra fullname: Batra, Mayank organization: Division of Pulmonary and Critical Care, University of Miami – sequence: 2 givenname: Runxia surname: Tian fullname: Tian, Runxia organization: Division of Pulmonary and Critical Care, University of Miami – sequence: 3 givenname: Chongxu surname: Zhang fullname: Zhang, Chongxu organization: Division of Pulmonary and Critical Care, University of Miami – sequence: 4 givenname: Emile surname: Clarence fullname: Clarence, Emile organization: School of Medicine, University of Miami – sequence: 5 givenname: Camila Sofia surname: Sacher fullname: Sacher, Camila Sofia organization: School of Medicine, University of Miami – sequence: 6 givenname: Justin Nestor surname: Miranda fullname: Miranda, Justin Nestor organization: School of Medicine, University of Miami – sequence: 7 givenname: Justin Rafa O. surname: De La Fuente fullname: De La Fuente, Justin Rafa O. organization: School of Medicine, University of Miami – sequence: 8 givenname: Megan surname: Mathew fullname: Mathew, Megan organization: School of Medicine, University of Miami – sequence: 9 givenname: Desmond surname: Green fullname: Green, Desmond organization: School of Medicine, University of Miami – sequence: 10 givenname: Sayari surname: Patel fullname: Patel, Sayari organization: School of Medicine, University of Miami – sequence: 11 givenname: Maria Virginia Perez surname: Bastidas fullname: Bastidas, Maria Virginia Perez organization: Division of Pulmonary and Critical Care, University of Miami – sequence: 12 givenname: Sara surname: Haddadi fullname: Haddadi, Sara organization: Division of Pulmonary and Critical Care, University of Miami – sequence: 13 givenname: Mukunthan surname: Murthi fullname: Murthi, Mukunthan organization: Division of Pulmonary and Critical Care, University of Miami – sequence: 14 givenname: Miguel Santiago surname: Gonzalez fullname: Gonzalez, Miguel Santiago organization: Division of Pulmonary and Critical Care, University of Miami – sequence: 15 givenname: Shweta surname: Kambali fullname: Kambali, Shweta organization: Division of Pulmonary and Critical Care, University of Miami – sequence: 16 givenname: Kayo H. M. surname: Santos fullname: Santos, Kayo H. M. organization: Division of Pulmonary and Critical Care, University of Miami – sequence: 17 givenname: Huda surname: Asif fullname: Asif, Huda organization: Division of Pulmonary and Critical Care, University of Miami – sequence: 18 givenname: Farzaneh surname: Modarresi fullname: Modarresi, Farzaneh organization: Express Gene Laboratory – sequence: 19 givenname: Mohammad surname: Faghihi fullname: Faghihi, Mohammad organization: Express Gene Laboratory – sequence: 20 givenname: Mehdi surname: Mirsaeidi fullname: Mirsaeidi, Mehdi email: msm249@med.miami.edu organization: Division of Pulmonary and Critical Care, University of Miami |
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/33568776$$D View this record in MEDLINE/PubMed |
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| Snippet | The Nucleocapsid Protein (N Protein) of severe acute respiratory syndrome Coronavirus 2 (SARS-CoV2) is located in the viral core. Immunoglobulin G (IgG)... Abstract The Nucleocapsid Protein (N Protein) of severe acute respiratory syndrome Coronavirus 2 (SARS-CoV2) is located in the viral core. Immunoglobulin G... |
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| Title | Role of IgG against N-protein of SARS-CoV2 in COVID19 clinical outcomes |
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