Your browser doesn't support javascript.
Severe COVID-19 is characterised by inflammation and immature myeloid cells early in disease progression.
Townsend, Liam; Dyer, Adam H; Naughton, Aifric; Imangaliyev, Sultan; Dunne, Jean; Kiersey, Rachel; Holden, Dean; Mooney, Aoife; Leavy, Deirdre; Ridge, Katie; Sugrue, Jamie; Aldoseri, Mubarak; Kelliher, Jo Hannah; Hennessy, Martina; Byrne, Declan; Browne, Paul; Bacon, Christopher L; Doyle, Catriona; O'Riordan, Ruth; McLaughlin, Anne-Marie; Bannan, Ciaran; Martin-Loeches, Ignacio; White, Arthur; McLoughlin, Rachel M; Bergin, Colm; Bourke, Nollaig M; O'Farrelly, Cliona; Conlon, Niall; Cheallaigh, Clíona Ní.
  • Townsend L; Department of Infectious Diseases, St James's Hospital, Dublin, Ireland.
  • Dyer AH; Department of Clinical Medicine, Trinity Translational Medicine Institute, Trinity College Dublin, Ireland.
  • Naughton A; Department of Medical Gerontology, Trinity Translational Medicine Institute, Trinity College Dublin, Ireland.
  • Imangaliyev S; Department of Immunology, St James's Hospital, Dublin, Ireland.
  • Dunne J; Host Pathogen Interactions Group, School of Biochemistry and Immunology, Trinity College Dublin, Ireland.
  • Kiersey R; Department of Immunology, St James's Hospital, Dublin, Ireland.
  • Holden D; Department of Immunology, St James's Hospital, Dublin, Ireland.
  • Mooney A; Department of Immunology, St James's Hospital, Dublin, Ireland.
  • Leavy D; Department of Immunology, St James's Hospital, Dublin, Ireland.
  • Ridge K; Department of Immunology, St James's Hospital, Dublin, Ireland.
  • Sugrue J; Department of Immunology, St James's Hospital, Dublin, Ireland.
  • Aldoseri M; School of Biochemistry and Immunology, Trinity College Dublin, Ireland.
  • Kelliher JH; Department of Intensive Care Medicine, St James's Hospital, Dublin, Ireland.
  • Hennessy M; Department of Intensive Care Medicine, St James's Hospital, Dublin, Ireland.
  • Byrne D; Clinical Research Facility, St James's Hospital, Dublin, Ireland.
  • Browne P; Department of General Medicine, St James's Hospital, Dublin, Ireland.
  • Bacon CL; Department of Haematology, St James's Hospital, Dublin, Ireland.
  • Doyle C; Department of Haematology, St James's Hospital, Dublin, Ireland.
  • O'Riordan R; Department of Infectious Diseases, St James's Hospital, Dublin, Ireland.
  • McLaughlin AM; Department of Infectious Diseases, St James's Hospital, Dublin, Ireland.
  • Bannan C; Department of Respiratory Medicine, St James's Hospital, Dublin.
  • Martin-Loeches I; Department of Infectious Diseases, St James's Hospital, Dublin, Ireland.
  • White A; Department of Intensive Care Medicine, St James's Hospital, Dublin, Ireland.
  • McLoughlin RM; School of Computer Science and Statistics, Trinity College Dublin, Ireland.
  • Bergin C; Host Pathogen Interactions Group, School of Biochemistry and Immunology, Trinity College Dublin, Ireland.
  • Bourke NM; Department of Infectious Diseases, St James's Hospital, Dublin, Ireland.
  • O'Farrelly C; Department of Clinical Medicine, Trinity Translational Medicine Institute, Trinity College Dublin, Ireland.
  • Conlon N; Department of Medical Gerontology, Trinity Translational Medicine Institute, Trinity College Dublin, Ireland.
  • Cheallaigh CN; School of Biochemistry and Immunology, Trinity College Dublin, Ireland.
Heliyon ; 8(4): e09230, 2022 Apr.
Article in English | MEDLINE | ID: covidwho-1768134
ABSTRACT
SARS-CoV-2 infection causes a wide spectrum of disease severity. Identifying the immunological characteristics of severe disease and the risk factors for their development are important in the management of COVID-19. This study aimed to identify and rank clinical and immunological features associated with progression to severe COVID-19 in order to investigate an immunological signature of severe disease. One hundred and eight patients with positive SARS-CoV-2 PCR were recruited. Routine clinical and laboratory markers were measured, as well as myeloid and lymphoid whole-blood immunophenotyping and measurement of the pro-inflammatory cytokines IL-6 and soluble CD25. All analysis was carried out in a routine hospital diagnostic laboratory. Univariate analysis demonstrated that severe disease was most strongly associated with elevated CRP and IL-6, loss of DLA-DR expression on monocytes and CD10 expression on neutrophils. Unbiased machine learning demonstrated that these four features were strongly associated with severe disease, with an average prediction score for severe disease of 0.925. These results demonstrate that these four markers could be used to identify patients developing severe COVID-19 and allow timely delivery of therapeutics.
Keywords

Full text: Available Collection: International databases Database: MEDLINE Type of study: Prognostic study Language: English Journal: Heliyon Year: 2022 Document Type: Article Affiliation country: J.heliyon.2022.e09230

Similar

MEDLINE

...
LILACS

LIS


Full text: Available Collection: International databases Database: MEDLINE Type of study: Prognostic study Language: English Journal: Heliyon Year: 2022 Document Type: Article Affiliation country: J.heliyon.2022.e09230