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Autoreactive T cells targeting type II pneumocyte antigens in COVID-19 convalescent patients.
Lichtensteiger, Christa; Koblischke, Maximilian; Berner, Fiamma; Jochum, Ann-Kristin; Sinnberg, Tobias; Balciunaite, Beatrice; Purde, Mette-Triin; Walter, Vincent; Abdou, Marie-Therese; Hofmeister, Kathrin; Kohler, Philipp; Vernazza, Pietro; Albrich, Werner C; Kahlert, Christian R; Zoufaly, Alexander; Traugott, Marianna T; Kern, Lukas; Pietsch, Urs; Kleger, Gian-Reto; Filipovic, Miodrag; Kneilling, Manfred; Cozzio, Antonio; Pop, Oltin; Bomze, David; Bergthaler, Andreas; Hasan Ali, Omar; Aberle, Judith; Flatz, Lukas.
Afiliação
  • Lichtensteiger C; Institute of Immunobiology, Kantonsspital St. Gallen, St. Gallen, Switzerland.
  • Koblischke M; Center for Virology, Medical University of Vienna, Vienna, Austria.
  • Berner F; Institute of Immunobiology, Kantonsspital St. Gallen, St. Gallen, Switzerland.
  • Jochum AK; Institute of Immunobiology, Kantonsspital St. Gallen, St. Gallen, Switzerland; Insitute of Pathology, Kantonsspital St. Gallen, St. Gallen, Switzerland.
  • Sinnberg T; Department of Dermatology, Eberhard Karls University Hospital Tübingen, Tübingen, Germany; Cluster of Excellence iFIT (EXC 2180) Image-Guided and Functionally Instructed Tumor Therapies, Eberhard Karls University Hospital Tübingen, Tübingen, Germany.
  • Balciunaite B; Department of Dermatology, Eberhard Karls University Hospital Tübingen, Tübingen, Germany.
  • Purde MT; Institute of Immunobiology, Kantonsspital St. Gallen, St. Gallen, Switzerland.
  • Walter V; Department of Dermatology, Eberhard Karls University Hospital Tübingen, Tübingen, Germany.
  • Abdou MT; Institute of Immunobiology, Kantonsspital St. Gallen, St. Gallen, Switzerland.
  • Hofmeister K; Department of Dermatology, Eberhard Karls University Hospital Tübingen, Tübingen, Germany.
  • Kohler P; Division of Infectious Diseases and Hospital Epidemiology, Kantonsspital St. Gallen, St. Gallen, Switzerland.
  • Vernazza P; Division of Infectious Diseases and Hospital Epidemiology, Kantonsspital St. Gallen, St. Gallen, Switzerland.
  • Albrich WC; Division of Infectious Diseases and Hospital Epidemiology, Kantonsspital St. Gallen, St. Gallen, Switzerland.
  • Kahlert CR; Division of Infectious Diseases and Hospital Epidemiology, Kantonsspital St. Gallen, St. Gallen, Switzerland.
  • Zoufaly A; Department of Medicine IV, Clinic Favoriten, Vienna Healthcare Group, Vienna, Austria; Faculty of Medicine, Sigmund Freud University Vienna, Austria.
  • Traugott MT; Department of Medicine IV, Clinic Favoriten, Vienna Healthcare Group, Vienna, Austria.
  • Kern L; Department of Pneumology, Kantonsspital St. Gallen, St. Gallen, Switzerland.
  • Pietsch U; Surgical Intensive Care Unit, Division of Anaesthesiology, Intensive Care, Rescue and Pain Medicine, Kantonsspital St. Gallen, Switzerland.
  • Kleger GR; Division of Intensive Care Medicine, Kantonsspital St. Gallen, Switzerland.
  • Filipovic M; Surgical Intensive Care Unit, Division of Anaesthesiology, Intensive Care, Rescue and Pain Medicine, Kantonsspital St. Gallen, Switzerland.
  • Kneilling M; Department of Dermatology, Eberhard Karls University Hospital Tübingen, Tübingen, Germany; Cluster of Excellence iFIT (EXC 2180) Image-Guided and Functionally Instructed Tumor Therapies, Eberhard Karls University Hospital Tübingen, Tübingen, Germany; Werner Siemens Imaging Center, Department of Prec
  • Cozzio A; Department of Dermatology, Venereology and Allergology, Kantonsspital St. Gallen, St. Gallen, Switzerland.
  • Pop O; Institute of Immunobiology, Kantonsspital St. Gallen, St. Gallen, Switzerland.
  • Bomze D; Institute of Immunobiology, Kantonsspital St. Gallen, St. Gallen, Switzerland; Sackler Faculty of Medicine, Tel Aviv University; Tel Aviv, Israel.
  • Bergthaler A; Institute for Hygiene and Applied Immunology, Center of Pathophysiology, Infectiology and Immunology, Medical University of Vienna, Austria; CeMM Research Center for Molecular Medicine or the Austrian Academy of Sciences, Vienna, Austria.
  • Hasan Ali O; Institute of Immunobiology, Kantonsspital St. Gallen, St. Gallen, Switzerland; Department of Dermatology, University Hospital Zurich, University of Zurich, Zurich, Switzerland; Department of Medical Genetics, Life Sciences Institute, University of British Columbia, Vancouver, Canada.
  • Aberle J; Center for Virology, Medical University of Vienna, Vienna, Austria.
  • Flatz L; Institute of Immunobiology, Kantonsspital St. Gallen, St. Gallen, Switzerland; Department of Dermatology, Eberhard Karls University Hospital Tübingen, Tübingen, Germany; Department of Dermatology, Venereology and Allergology, Kantonsspital St. Gallen, St. Gallen, Switzerland; Department of Dermatolo
J Autoimmun ; 140: 103118, 2023 Oct 10.
Article em En | MEDLINE | ID: mdl-37826919
ABSTRACT

BACKGROUND:

The role of autoreactive T cells on the course of Coronavirus disease-19 (COVID-19) remains elusive. Type II pneumocytes represent the main target cells of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Autoimmune responses against antigens highly expressed in type II pneumocytes may influence the severity of COVID-19 disease.

OBJECTIVE:

The aim of this study was to investigate autoreactive T cell responses against self-antigens highly expressed in type II pneumocytes in the blood of COVID-19 patients with severe and non-severe disease.

METHODS:

We collected blood samples of COVID-19 patients with varying degrees of disease severity and of pre-pandemic controls. T cell stimulation assays with peptide pools of type II pneumocyte antigens were performed in two independent cohorts to analyze the autoimmune T cell responses in patients with non-severe and severe COVID-19 disease. Target cell lysis assays were performed with lung cancer cell lines to determine the extent of cell killing by type II PAA-specific T cells.

RESULTS:

We identified autoreactive T cell responses against four recently described self-antigens highly expressed in type II pneumocytes, known as surfactant protein A, surfactant protein B, surfactant protein C and napsin A, in the blood of COVID-19 patients. These antigens were termed type II pneumocyte-associated antigens (type II PAAs). We found that patients with non-severe COVID-19 disease showed a significantly higher frequency of type II PAA-specific autoreactive T cells in the blood when compared to severely ill patients. The presence of high frequencies of type II PAA-specific T cells in the blood of non-severe COVID-19 patients was independent of their age. We also found that napsin A-specific T cells from convalescent COVID-19 patients could kill lung cancer cells, demonstrating the functional and cytotoxic role of these T cells.

CONCLUSIONS:

Our data suggest that autoreactive type II PAA-specific T cells have a protective role in SARS-CoV-2 infections and the presence of high frequencies of these autoreactive T cells indicates effective viral control in COVID-19 patients. Type II-PAA-specific T cells may therefore promote the killing of infected type II pneumocytes and viral clearance.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article