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Reduced humoral but stable cellular SARS-CoV-2-specific immunity in liver transplant recipients in the first year after COVID-19.
Kirchner, Theresa; Heinrich, Sophia; Bonifacius, Agnes; Engel, Bastian; Ruhl, Louisa; Pink, Isabell; Thomas, Nele; Martens, Joerg; Hoeper, Marius M; Blasczyk, Rainer; Wedemeyer, Heiner; Jaeckel, Elmar; Li, Yang; Falk, Christine S; Eiz-Vesper, Britta; Taubert, Richard.
  • Kirchner T; Department of Gastroenterology, Hepatology and Endocrinology, Hannover Medical School, Hannover, Germany.
  • Heinrich S; Department of Gastroenterology, Hepatology and Endocrinology, Hannover Medical School, Hannover, Germany.
  • Bonifacius A; Institute of Transfusion Medicine and Transplant Engineering, Hannover Medical School, Hannover, Germany.
  • Engel B; Department of Gastroenterology, Hepatology and Endocrinology, Hannover Medical School, Hannover, Germany.
  • Ruhl L; Institute of Transplant Immunology, Hannover Medical School, Hannover, Germany.
  • Pink I; Department of Pneumology, Hannover Medical School, member of the German Centre for Lung Research (DZL), Hannover, Germany.
  • Thomas N; Institute of Biostatistics, Hannover Medical School, Hannover, Germany.
  • Martens J; Institute of Transfusion Medicine and Transplant Engineering, Hannover Medical School, Hannover, Germany.
  • Hoeper MM; Department of Pneumology, Hannover Medical School, member of the German Centre for Lung Research (DZL), Hannover, Germany.
  • Blasczyk R; Institute of Transfusion Medicine and Transplant Engineering, Hannover Medical School, Hannover, Germany.
  • Wedemeyer H; Department of Gastroenterology, Hepatology and Endocrinology, Hannover Medical School, Hannover, Germany.
  • Jaeckel E; Department of Gastroenterology, Hepatology and Endocrinology, Hannover Medical School, Hannover, Germany.
  • Li Y; Department for Liver Transplantation at University Health Network of the University of Toronto, Toronto, Canada.
  • Falk CS; Centre for Individualised Infection Medicine and TWINCORE, Joint Ventures between the Hannover Medical School and the Helmholtz Centre for Infection Research, Hannover, Germany.
  • Eiz-Vesper B; Institute of Transplant Immunology, Hannover Medical School, Hannover, Germany.
  • Taubert R; Institute of Transfusion Medicine and Transplant Engineering, Hannover Medical School, Hannover, Germany.
PLoS One ; 17(11): e0276929, 2022.
Article in English | MEDLINE | ID: covidwho-2098767
ABSTRACT
Mortality due to COVID-19 is not increased in immunosuppressed individuals after liver transplantation (OLT) compared to individuals without immunosuppression. Data on long-term protective immunity against SARS-CoV-2 in immunosuppressed convalescents, is limited. We prospectively measured immune responses against SARS-CoV-2 by quantifying antibodies against 4 different antigens (spike protein 1 and 2, receptor binding domain, nucleocapsid) and T cell responses by IFN-γ ELISPOT against 4 antigens (membrane, nucleocapsid, spike protein 1 and 2) in 24 OLT convalescents with immunosuppressive therapy longitudinally in the first year after COVID-19 including a booster vaccination in comparison to a matched cohort of non-immunosuppressed convalescents (non-IS-Con). Pre-pandemic OLT samples were retrieved from our prospective OLT biorepository (n = 16). No relevant T cell reactivity or immunoglobulin G (IgG) against SARS-CoV-2 were detectable in pre-pandemic samples of OLT recipients despite reactivity against endemic corona-viruses. OLT convalescents had a lower prevalence of IgG against nucleocapsid (54% vs. 90%) but not against spike protein domains (98-100% vs. 100%) after vaccination in the second half-year after COVID-19 compared to non-IS-Con. Also, concentrations of anti-nucleocapsid IgG were lower in OLT convalescents than in non-IS-Con. Concentration of IgG against spike protein domains was significantly increased by a booster vaccination in OLT convalescents. But concentration of IgG against two of three spike protein domains remains slightly lower compared to non-IS-Con finally. However, none of these differences was mirrored by the cellular immunity against SARS-CoV-2 that remained stable during the first year after COVID-19 and was not further stimulated by a corona vaccination in OLT convalescents. In conclusion, despite lower concentrations of anti-SARS-CoV-2 IgG in OLT convalescents anti-SARS-CoV-2 cellular immunity was as robust as in non-IS-Con.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Liver Transplantation / COVID-19 Type of study: Cohort study / Observational study / Prognostic study Topics: Vaccines Limits: Humans Language: English Journal: PLoS One Journal subject: Science / Medicine Year: 2022 Document Type: Article Affiliation country: Journal.pone.0276929

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Liver Transplantation / COVID-19 Type of study: Cohort study / Observational study / Prognostic study Topics: Vaccines Limits: Humans Language: English Journal: PLoS One Journal subject: Science / Medicine Year: 2022 Document Type: Article Affiliation country: Journal.pone.0276929