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Immunosuppression and SARS-CoV-2 Infection in Kidney Transplant Recipients.

Authors :
UCL - SSS/IREC/NEFR - Pôle de Néphrologie
UCL - (SLuc) Service de néphrologie
UCL - SSS/IREC - Institut de recherche expérimentale et clinique
UCL - (SLuc) Département de médecine interne et services associés
Devresse, Arnaud
De Greef, Julien
Yombi, Jean Cyr
Belkhir, Leïla
Goffin, Eric
Kanaan, Nada
UCL - SSS/IREC/NEFR - Pôle de Néphrologie
UCL - (SLuc) Service de néphrologie
UCL - SSS/IREC - Institut de recherche expérimentale et clinique
UCL - (SLuc) Département de médecine interne et services associés
Devresse, Arnaud
De Greef, Julien
Yombi, Jean Cyr
Belkhir, Leïla
Goffin, Eric
Kanaan, Nada
Source :
Transplantation direct, Vol. 8, no.3, p. e1292 (2022)
Publication Year :
2022

Abstract

Kidney transplant recipients (KTRs) infected with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) may have an increased risk of mortality compared with the general population and hemodialysis patients. As these patients are immunosuppressed, it might seem obvious to attribute this excess mortality to the impaired immunity induced by immunosuppression. In line with this reasoning is the low immune response, both cellular and humoral, that KTRs mount in response to the anti-SARS-CoV-2 vaccine; however, acute respiratory distress syndrome associated with coronavirus disease 2019 is triggered by a state of inflammation and cytokine release syndrome that lead to pulmonary damage and increased mortality. In that context, immunosuppressive treatment dampening the immune response could, in theory, be potentially beneficial. This review aims at analyzing the current knowledge on the impact of immunosuppressive treatment on mortality in SARS-CoV-2-infected KTRs, the optimal management of immunosuppression in the coronavirus disease 2019 era, and the vaccine response and management in immunosuppressed KTRs.

Details

Database :
OAIster
Journal :
Transplantation direct, Vol. 8, no.3, p. e1292 (2022)
Notes :
English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1328222858
Document Type :
Electronic Resource