SARS-CoV-2 infection in dialysis and kidney transplant patients: immunological and serological response
Background Dialysis and kidney transplant patients with moderate-severe COVID-19 have a high mortality rate, around 30%, that is similar in the two populations, despite differences in their baseline characteristics. In these groups, the immunology of the disease has been poorly explored. Methods Thirty-two patients on dialysis or with kidney transplant and SARS-CoV-2 infection requiring hospitalization (COV group) were included in our study. Lymphocyte subsets, dendritic cell (DC) counts and monocyte activation were studied. SARS-CoV-2 anti-spike/anti-nucleocapsid were monitored, and baseline cytokines and chemokines were measured in 10 patients. Results The COV group, compared to healthy subjects and uninfected dialysis/kidney transplant controls, showed lower numbers of CD4 + and CD8 + T cells, Natural-Killer (NK), B cells, plasmacytoid and myeloid DCs, while the proportion of terminally differentiated B-cells was increased. IL6, IL10, IFN-α and chemokines involved in monocyte and neutrophil recruitment were higher in the COV group, compared to uninfected dialysis/kidney transplant controls. Patients with severe disease had lower CD4 + , CD8 + and B-cell counts and lower monocyte HLA-DR expression. Of note, when comparing dialysis and kidney transplant patients with COVID-19, the latter group presented lower NK and pDC counts and monocyte HLA-DR expression. Up to 60 days after symptom onset, kidney transplant recipients showed lower levels of anti-spike antibodies compared to dialysis patients. Conclusions During SARS-CoV-2 infection, dialysis and kidney transplant patients manifest immunophenotype abnormalities; these are similar in the two groups, however kidney transplant recipients show more profound alterations of the innate immune system and lower anti-spike antibody response. Graphical abstract.
Medienart: |
E-Artikel |
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Erscheinungsjahr: |
2022 |
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Erschienen: |
2022 |
Enthalten in: |
Zur Gesamtaufnahme - volume:35 |
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Enthalten in: |
Journal of nephrology - 35(2022), 3 vom: 24. Jan., Seite 745-759 |
Sprache: |
Englisch |
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Beteiligte Personen: |
Alberici, Federico [VerfasserIn] |
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Links: |
Volltext [lizenzpflichtig] |
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Themen: |
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Anmerkungen: |
© The Author(s) under exclusive licence to Italian Society of Nephrology 2021 |
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doi: |
10.1007/s40620-021-01214-8 |
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funding: |
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PPN (Katalog-ID): |
OLC2130109721 |
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520 | |a Background Dialysis and kidney transplant patients with moderate-severe COVID-19 have a high mortality rate, around 30%, that is similar in the two populations, despite differences in their baseline characteristics. In these groups, the immunology of the disease has been poorly explored. Methods Thirty-two patients on dialysis or with kidney transplant and SARS-CoV-2 infection requiring hospitalization (COV group) were included in our study. Lymphocyte subsets, dendritic cell (DC) counts and monocyte activation were studied. SARS-CoV-2 anti-spike/anti-nucleocapsid were monitored, and baseline cytokines and chemokines were measured in 10 patients. Results The COV group, compared to healthy subjects and uninfected dialysis/kidney transplant controls, showed lower numbers of CD4 + and CD8 + T cells, Natural-Killer (NK), B cells, plasmacytoid and myeloid DCs, while the proportion of terminally differentiated B-cells was increased. IL6, IL10, IFN-α and chemokines involved in monocyte and neutrophil recruitment were higher in the COV group, compared to uninfected dialysis/kidney transplant controls. Patients with severe disease had lower CD4 + , CD8 + and B-cell counts and lower monocyte HLA-DR expression. Of note, when comparing dialysis and kidney transplant patients with COVID-19, the latter group presented lower NK and pDC counts and monocyte HLA-DR expression. Up to 60 days after symptom onset, kidney transplant recipients showed lower levels of anti-spike antibodies compared to dialysis patients. Conclusions During SARS-CoV-2 infection, dialysis and kidney transplant patients manifest immunophenotype abnormalities; these are similar in the two groups, however kidney transplant recipients show more profound alterations of the innate immune system and lower anti-spike antibody response. Graphical abstract | ||
650 | 4 | |a Hemodialysis | |
650 | 4 | |a Kidney transplant | |
650 | 4 | |a Lymphocytes | |
650 | 4 | |a SARS-CoV-2 | |
650 | 4 | |a COVID-19 | |
700 | 1 | |a Affatato, Stefania |4 aut | |
700 | 1 | |a Moratto, Daniele |4 aut | |
700 | 1 | |a Mescia, Federica |4 aut | |
700 | 1 | |a Delbarba, Elisa |4 aut | |
700 | 1 | |a Guerini, Alice |4 aut | |
700 | 1 | |a Tedesco, Martina |4 aut | |
700 | 1 | |a Burbelo, Peter D. |4 aut | |
700 | 1 | |a Zani, Roberta |4 aut | |
700 | 1 | |a Castagna, Ilaria |4 aut | |
700 | 1 | |a Gallico, Agnese |4 aut | |
700 | 1 | |a Tonoli, Mattia |4 aut | |
700 | 1 | |a Venturini, Margherita |4 aut | |
700 | 1 | |a Roccaro, Aldo M. |4 aut | |
700 | 1 | |a Giacomelli, Mauro |4 aut | |
700 | 1 | |a Cohen, Jeffrey I. |4 aut | |
700 | 1 | |a Giustini, Viviana |4 aut | |
700 | 1 | |a Dobbs, Kerry |4 aut | |
700 | 1 | |a Su, Helen C. |4 aut | |
700 | 1 | |a Fiorini, Chiara |4 aut | |
700 | 1 | |a Quaresima, Virginia |4 aut | |
700 | 1 | |a Viola, Fabio Battista |4 aut | |
700 | 1 | |a Vizzardi, Valerio |4 aut | |
700 | 1 | |a Gaggiotti, Mario |4 aut | |
700 | 1 | |a Bossini, Nicola |4 aut | |
700 | 1 | |a Gaggia, Paola |4 aut | |
700 | 1 | |a Badolato, Raffaele |4 aut | |
700 | 1 | |a Notarangelo, Luigi D. |4 aut | |
700 | 1 | |a Chiarini, Marco |4 aut | |
700 | 1 | |a Scolari, Francesco |4 aut | |
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