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Impaired immune responses and prolonged viral replication in lung allograft recipients infected with SARS-CoV-2 in the early phase after transplantation.
Glueck, Olaf M; Liang, Xiaoling; Badell, Irina; Wratil, Paul R; Graf, Alexander; Krebs, Stefan; Blum, Helmut; Hellmuth, Johannes C; Scherer, Clemens; Hollaus, Alexandra; Spaeth, Patricia M; Karakoc, Burak; Fuchs, Thimo; Zimmermann, Julia; Kauke, Teresa; Moosmann, Andreas; Keppler, Oliver T; Schneider, Christian; Muenchhoff, Maximilian.
Afiliação
  • Glueck OM; Division of Thoracic Surgery, LMU University Hospital, LMU Munich, Munich, Germany.
  • Liang X; Max Von Pettenkofer Institute and Gene Center, Virology, National Reference Center for Retroviruses, Ludwig Maximilian University of Munich, Pettenkoferstr. 9a, 80336, Munich, Germany.
  • Badell I; Max Von Pettenkofer Institute and Gene Center, Virology, National Reference Center for Retroviruses, Ludwig Maximilian University of Munich, Pettenkoferstr. 9a, 80336, Munich, Germany.
  • Wratil PR; Max Von Pettenkofer Institute and Gene Center, Virology, National Reference Center for Retroviruses, Ludwig Maximilian University of Munich, Pettenkoferstr. 9a, 80336, Munich, Germany.
  • Graf A; German Center for Infection Research (DZIF), Partner Site, Munich, Germany.
  • Krebs S; Laboratory for Functional Genome Analysis, Gene Center, Ludwig Maximilian University of Munich, Munich, Germany.
  • Blum H; Laboratory for Functional Genome Analysis, Gene Center, Ludwig Maximilian University of Munich, Munich, Germany.
  • Hellmuth JC; Laboratory for Functional Genome Analysis, Gene Center, Ludwig Maximilian University of Munich, Munich, Germany.
  • Scherer C; Department of Medicine III, LMU University Hospital, LMU Munich, Munich, Germany.
  • Hollaus A; Department of Medicine I, LMU University Hospital, LMU Munich, Munich, Germany.
  • Spaeth PM; Department of Medicine III, LMU University Hospital, LMU Munich, Munich, Germany.
  • Karakoc B; Helmholtz Munich, Munich, Germany.
  • Fuchs T; Max Von Pettenkofer Institute and Gene Center, Virology, National Reference Center for Retroviruses, Ludwig Maximilian University of Munich, Pettenkoferstr. 9a, 80336, Munich, Germany.
  • Zimmermann J; Max Von Pettenkofer Institute and Gene Center, Virology, National Reference Center for Retroviruses, Ludwig Maximilian University of Munich, Pettenkoferstr. 9a, 80336, Munich, Germany.
  • Kauke T; Max Von Pettenkofer Institute and Gene Center, Virology, National Reference Center for Retroviruses, Ludwig Maximilian University of Munich, Pettenkoferstr. 9a, 80336, Munich, Germany.
  • Moosmann A; Division of Thoracic Surgery, LMU University Hospital, LMU Munich, Munich, Germany.
  • Keppler OT; Division of Thoracic Surgery, LMU University Hospital, LMU Munich, Munich, Germany.
  • Schneider C; German Center for Infection Research (DZIF), Partner Site, Munich, Germany.
  • Muenchhoff M; Department of Medicine III, LMU University Hospital, LMU Munich, Munich, Germany.
Infection ; 2023 Nov 03.
Article em En | MEDLINE | ID: mdl-37922037
ABSTRACT

PURPOSE:

Lung transplant recipients are at increased risk of severe disease following infection with severe acute respiratory syndrome coronavirus type 2 (SARS-CoV-2) due to high-dose immunosuppressive drugs and the lung is the main organ affected by Coronavirus disease 2019 (COVID-19). Several studies have confirmed increased SARS-CoV-2-related mortality and morbidity in patients living with lung allografts; however, detailed immunological studies of patients with SARS-CoV-2 infection in the early phase following transplantation remain scarce.

METHODS:

We investigated patients who were infected with SARS-CoV-2 in the early phase (18-103 days) after receiving double-lung allografts (n = 4, LuTx) in comparison to immunocompetent patients who had not received solid organ transplants (n = 88, noTx). We analyzed SARS-CoV-2-specific antibody responses against the SARS-CoV-2 spike and nucleocapsid proteins using enzyme-linked immunosorbent assays (ELISA), chemiluminescence immunoassays (CLIA), and immunoblot assays. T cell responses were investigated using Elispot assays.

RESULTS:

One LuTx patient suffered from persistent infection with fatal outcome 122 days post-infection despite multiple interventions including remdesivir, convalescent plasma, and the monoclonal antibody bamlanivimab. Two patients experienced clinically mild disease with prolonged viral shedding (47 and 79 days), and one patient remained asymptomatic. Antibody and T cell responses were significantly reduced or undetectable in all LuTx patients compared to noTx patients.

CONCLUSION:

Patients in the early phase following lung allograft transplantation are vulnerable to infection with SARS-CoV-2 due to impaired immune responses. This patient population should be vaccinated before LuTx, protected from infection post-LuTx, and in case of infection treated generously with currently available interventions.
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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