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Immuno-proteomic profiling reveals aberrant immune cell regulation in the airways of individuals with ongoing post-COVID-19 respiratory disease.
Vijayakumar, Bavithra; Boustani, Karim; Ogger, Patricia P; Papadaki, Artemis; Tonkin, James; Orton, Christopher M; Ghai, Poonam; Suveizdyte, Kornelija; Hewitt, Richard J; Desai, Sujal R; Devaraj, Anand; Snelgrove, Robert J; Molyneaux, Philip L; Garner, Justin L; Peters, James E; Shah, Pallav L; Lloyd, Clare M; Harker, James A.
  • Vijayakumar B; National Heart and Lung Institute, Imperial College London, London, UK; Chelsea and Westminster Hospital, London, UK; Royal Brompton and Harefield Hospitals, Guy's and St Thomas' NHS Foundation Trust, London, UK.
  • Boustani K; National Heart and Lung Institute, Imperial College London, London, UK; Asthma UK Centre for Allergic Mechanisms of Asthma, London, London, UK.
  • Ogger PP; National Heart and Lung Institute, Imperial College London, London, UK.
  • Papadaki A; Centre for Inflammatory Disease, Department of Immunology and Inflammation, Imperial College London, London, UK.
  • Tonkin J; National Heart and Lung Institute, Imperial College London, London, UK; Royal Brompton and Harefield Hospitals, Guy's and St Thomas' NHS Foundation Trust, London, UK.
  • Orton CM; National Heart and Lung Institute, Imperial College London, London, UK; Royal Brompton and Harefield Hospitals, Guy's and St Thomas' NHS Foundation Trust, London, UK.
  • Ghai P; National Heart and Lung Institute, Imperial College London, London, UK.
  • Suveizdyte K; National Heart and Lung Institute, Imperial College London, London, UK.
  • Hewitt RJ; National Heart and Lung Institute, Imperial College London, London, UK; Royal Brompton and Harefield Hospitals, Guy's and St Thomas' NHS Foundation Trust, London, UK.
  • Desai SR; National Heart and Lung Institute, Imperial College London, London, UK; Royal Brompton and Harefield Hospitals, Guy's and St Thomas' NHS Foundation Trust, London, UK; Margaret Turner-Warwick Centre for Fibrosing Lung Diseases, London, UK.
  • Devaraj A; National Heart and Lung Institute, Imperial College London, London, UK; Royal Brompton and Harefield Hospitals, Guy's and St Thomas' NHS Foundation Trust, London, UK.
  • Snelgrove RJ; National Heart and Lung Institute, Imperial College London, London, UK; Asthma UK Centre for Allergic Mechanisms of Asthma, London, London, UK.
  • Molyneaux PL; National Heart and Lung Institute, Imperial College London, London, UK; Royal Brompton and Harefield Hospitals, Guy's and St Thomas' NHS Foundation Trust, London, UK.
  • Garner JL; Chelsea and Westminster Hospital, London, UK; Royal Brompton and Harefield Hospitals, Guy's and St Thomas' NHS Foundation Trust, London, UK.
  • Peters JE; Centre for Inflammatory Disease, Department of Immunology and Inflammation, Imperial College London, London, UK.
  • Shah PL; National Heart and Lung Institute, Imperial College London, London, UK; Chelsea and Westminster Hospital, London, UK; Royal Brompton and Harefield Hospitals, Guy's and St Thomas' NHS Foundation Trust, London, UK.
  • Lloyd CM; National Heart and Lung Institute, Imperial College London, London, UK; Asthma UK Centre for Allergic Mechanisms of Asthma, London, London, UK.
  • Harker JA; National Heart and Lung Institute, Imperial College London, London, UK; Asthma UK Centre for Allergic Mechanisms of Asthma, London, London, UK. Electronic address: j.harker@imperial.ac.uk.
Immunity ; 55(3): 542-556.e5, 2022 03 08.
Article in English | MEDLINE | ID: covidwho-1768197
ABSTRACT
Some patients hospitalized with acute COVID-19 suffer respiratory symptoms that persist for many months. We delineated the immune-proteomic landscape in the airways and peripheral blood of healthy controls and post-COVID-19 patients 3 to 6 months after hospital discharge. Post-COVID-19 patients showed abnormal airway (but not plasma) proteomes, with an elevated concentration of proteins associated with apoptosis, tissue repair, and epithelial injury versus healthy individuals. Increased numbers of cytotoxic lymphocytes were observed in individuals with greater airway dysfunction, while increased B cell numbers and altered monocyte subsets were associated with more widespread lung abnormalities. A one-year follow-up of some post-COVID-19 patients indicated that these abnormalities resolved over time. In summary, COVID-19 causes a prolonged change to the airway immune landscape in those with persistent lung disease, with evidence of cell death and tissue repair linked to the ongoing activation of cytotoxic T cells.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Respiration Disorders / Respiratory System / B-Lymphocytes / Monocytes / T-Lymphocytes, Cytotoxic / SARS-CoV-2 / COVID-19 Type of study: Cohort study / Prognostic study Topics: Long Covid Limits: Adult / Aged / Female / Humans / Male / Middle aged Language: English Journal: Immunity Journal subject: Allergy and Immunology Year: 2022 Document Type: Article Affiliation country: J.immuni.2022.01.017

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Respiration Disorders / Respiratory System / B-Lymphocytes / Monocytes / T-Lymphocytes, Cytotoxic / SARS-CoV-2 / COVID-19 Type of study: Cohort study / Prognostic study Topics: Long Covid Limits: Adult / Aged / Female / Humans / Male / Middle aged Language: English Journal: Immunity Journal subject: Allergy and Immunology Year: 2022 Document Type: Article Affiliation country: J.immuni.2022.01.017