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Monoclonal Antibody Therapy in Kidney Transplant Recipients With Delta and Omicron Variants of SARS-CoV-2: A Single-Center Case Series

RATIONALE & OBJECTIVE: Neutralizing monoclonal antibody treatments have shown promising preliminary results in kidney transplant recipients infected with severe acute respiratory syndrome coronavirus 2. However, their efficacy in kidney transplant recipients infected with the Omicron variant has...

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Autores principales: Fernandes, Guillaume, Devresse, Arnaud, Scohy, Anais, De Greef, Julien, Yombi, Jean Cyr, Belkhir, Leila, Darius, Tom, Mourad, Michel, Buemi, Antoine, Kabamba, Benoit, Goffin, Eric, Kanaan, Nada
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9042411/
https://www.ncbi.nlm.nih.gov/pubmed/35493029
http://dx.doi.org/10.1016/j.xkme.2022.100470
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author Fernandes, Guillaume
Devresse, Arnaud
Scohy, Anais
De Greef, Julien
Yombi, Jean Cyr
Belkhir, Leila
Darius, Tom
Mourad, Michel
Buemi, Antoine
Kabamba, Benoit
Goffin, Eric
Kanaan, Nada
author_facet Fernandes, Guillaume
Devresse, Arnaud
Scohy, Anais
De Greef, Julien
Yombi, Jean Cyr
Belkhir, Leila
Darius, Tom
Mourad, Michel
Buemi, Antoine
Kabamba, Benoit
Goffin, Eric
Kanaan, Nada
author_sort Fernandes, Guillaume
collection PubMed
description RATIONALE & OBJECTIVE: Neutralizing monoclonal antibody treatments have shown promising preliminary results in kidney transplant recipients infected with severe acute respiratory syndrome coronavirus 2. However, their efficacy in kidney transplant recipients infected with the Omicron variant has not been reported yet. STUDY DESIGN: Single-center retrospective study. SETTING & PARTICIPANTS: We included all consecutive kidney transplant recipients treated with monoclonal antibodies for severe acute respiratory syndrome coronavirus 2 infections (positive polymerase chain reaction on nasopharyngeal swab) between June 10, 2021, and January 14, 2022. Forty-seven kidney transplant recipients were included. All patients had symptoms evolving for ≤7 days and no oxygen therapy need at monoclonal antibody infusion. RESULTS: Symptoms at diagnosis were mainly cough (n = 25; 53%) and fever (n = 15; 32%). Eighty-three percent of the cohort (n = 39) had been vaccinated with at least 2 doses before infection, of whom 30 (77%) had demonstrated a vaccine-induced humoral response. They were treated with either casirivimab-imdevimab (n = 16; 34%) or sotrovimab (n = 31; 66%) a median of 2 days (range, 0-6 days) after the onset of symptoms. Except for 1 mild allergic reaction during casirivimab-imdevimab infusion, no side effects were reported. The median viral loads at admission (day 0) and 7 days after monoclonal antibody infusion were 2,110,027 copies/mL (range, 1,000-153,798,962 copies/mL) and 1,000 copies/mL (range, 0-10,000,000 copies/mL), respectively. Genotypes were available for 22 kidney transplant recipients (47%). Omicron, Delta, and Gamma variants were identified in 13 (59%), 8 (36%), and 1 (5%) patients, respectively. In kidney transplant recipients infected with the Omicron variant, the median viral loads at day 0 and day 7 were 752,789 copies/mL (range, 4,000-12,859,300 copies/mL) and 1,353 copies/mL (range, 0-1,211,163 copies/mL), respectively. 2 kidney transplant recipients required hospitalization immediately after sotrovimab perfusion for oxygen therapy that was weaned in 3 days, allowing patients’ discharge. None were admitted to the intensive care unit or died. LIMITATIONS: Small sample size, no control group. CONCLUSIONS: Neutralizing monoclonal antibody therapy is associated with positive outcomes in kidney transplant recipients with mild coronavirus disease 2019, including those infected with the Omicron variant.
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spelling pubmed-90424112022-04-27 Monoclonal Antibody Therapy in Kidney Transplant Recipients With Delta and Omicron Variants of SARS-CoV-2: A Single-Center Case Series Fernandes, Guillaume Devresse, Arnaud Scohy, Anais De Greef, Julien Yombi, Jean Cyr Belkhir, Leila Darius, Tom Mourad, Michel Buemi, Antoine Kabamba, Benoit Goffin, Eric Kanaan, Nada Kidney Med Original Research RATIONALE & OBJECTIVE: Neutralizing monoclonal antibody treatments have shown promising preliminary results in kidney transplant recipients infected with severe acute respiratory syndrome coronavirus 2. However, their efficacy in kidney transplant recipients infected with the Omicron variant has not been reported yet. STUDY DESIGN: Single-center retrospective study. SETTING & PARTICIPANTS: We included all consecutive kidney transplant recipients treated with monoclonal antibodies for severe acute respiratory syndrome coronavirus 2 infections (positive polymerase chain reaction on nasopharyngeal swab) between June 10, 2021, and January 14, 2022. Forty-seven kidney transplant recipients were included. All patients had symptoms evolving for ≤7 days and no oxygen therapy need at monoclonal antibody infusion. RESULTS: Symptoms at diagnosis were mainly cough (n = 25; 53%) and fever (n = 15; 32%). Eighty-three percent of the cohort (n = 39) had been vaccinated with at least 2 doses before infection, of whom 30 (77%) had demonstrated a vaccine-induced humoral response. They were treated with either casirivimab-imdevimab (n = 16; 34%) or sotrovimab (n = 31; 66%) a median of 2 days (range, 0-6 days) after the onset of symptoms. Except for 1 mild allergic reaction during casirivimab-imdevimab infusion, no side effects were reported. The median viral loads at admission (day 0) and 7 days after monoclonal antibody infusion were 2,110,027 copies/mL (range, 1,000-153,798,962 copies/mL) and 1,000 copies/mL (range, 0-10,000,000 copies/mL), respectively. Genotypes were available for 22 kidney transplant recipients (47%). Omicron, Delta, and Gamma variants were identified in 13 (59%), 8 (36%), and 1 (5%) patients, respectively. In kidney transplant recipients infected with the Omicron variant, the median viral loads at day 0 and day 7 were 752,789 copies/mL (range, 4,000-12,859,300 copies/mL) and 1,353 copies/mL (range, 0-1,211,163 copies/mL), respectively. 2 kidney transplant recipients required hospitalization immediately after sotrovimab perfusion for oxygen therapy that was weaned in 3 days, allowing patients’ discharge. None were admitted to the intensive care unit or died. LIMITATIONS: Small sample size, no control group. CONCLUSIONS: Neutralizing monoclonal antibody therapy is associated with positive outcomes in kidney transplant recipients with mild coronavirus disease 2019, including those infected with the Omicron variant. Elsevier 2022-04-27 /pmc/articles/PMC9042411/ /pubmed/35493029 http://dx.doi.org/10.1016/j.xkme.2022.100470 Text en © 2022 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Research
Fernandes, Guillaume
Devresse, Arnaud
Scohy, Anais
De Greef, Julien
Yombi, Jean Cyr
Belkhir, Leila
Darius, Tom
Mourad, Michel
Buemi, Antoine
Kabamba, Benoit
Goffin, Eric
Kanaan, Nada
Monoclonal Antibody Therapy in Kidney Transplant Recipients With Delta and Omicron Variants of SARS-CoV-2: A Single-Center Case Series
title Monoclonal Antibody Therapy in Kidney Transplant Recipients With Delta and Omicron Variants of SARS-CoV-2: A Single-Center Case Series
title_full Monoclonal Antibody Therapy in Kidney Transplant Recipients With Delta and Omicron Variants of SARS-CoV-2: A Single-Center Case Series
title_fullStr Monoclonal Antibody Therapy in Kidney Transplant Recipients With Delta and Omicron Variants of SARS-CoV-2: A Single-Center Case Series
title_full_unstemmed Monoclonal Antibody Therapy in Kidney Transplant Recipients With Delta and Omicron Variants of SARS-CoV-2: A Single-Center Case Series
title_short Monoclonal Antibody Therapy in Kidney Transplant Recipients With Delta and Omicron Variants of SARS-CoV-2: A Single-Center Case Series
title_sort monoclonal antibody therapy in kidney transplant recipients with delta and omicron variants of sars-cov-2: a single-center case series
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9042411/
https://www.ncbi.nlm.nih.gov/pubmed/35493029
http://dx.doi.org/10.1016/j.xkme.2022.100470
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