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

COVID-19 ESKD Omicron SARS-CoV-2 hospitalization kidney transplant monoclonal antibody

Journal

Kidney medicine
ISSN: 2590-0595
Titre abrégé: Kidney Med
Pays: United States
ID NLM: 101756300

Informations de publication

Date de publication:
Jun 2022
Historique:
pubmed: 3 5 2022
medline: 3 5 2022
entrez: 2 5 2022
Statut: ppublish

Résumé

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. Single-center retrospective study. 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. 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. Small sample size, no control group. 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.

Identifiants

pubmed: 35493029
doi: 10.1016/j.xkme.2022.100470
pii: S2590-0595(22)00084-X
pmc: PMC9042411
doi:

Types de publication

Journal Article

Langues

eng

Pagination

100470

Informations de copyright

© 2022 The Authors.

Références

Lancet. 2022 Feb 12;399(10325):665-676
pubmed: 35151397
JAMA. 2022 Apr 5;327(13):1236-1246
pubmed: 35285853
N Engl J Med. 2021 Jan 21;384(3):229-237
pubmed: 33113295
Transplantation. 2021 Dec 1;105(12):e282
pubmed: 34456266
Transplantation. 2022 Jan 1;106(1):e107-e108
pubmed: 34711781
MMWR Morb Mortal Wkly Rep. 2022 Feb 04;71(5):177-181
pubmed: 35113851
Kidney Int. 2020 Dec;98(6):1540-1548
pubmed: 32979369
N Engl J Med. 2021 Nov 18;385(21):1941-1950
pubmed: 34706189
Lancet. 2022 Jan 29;399(10323):437-446
pubmed: 35065011
Transplantation. 2021 Nov 1;105(11):e265-e266
pubmed: 34310531
Kidney Int. 2022 Mar;101(3):645-646
pubmed: 34995651
Transplantation. 2021 Oct 1;105(10):e146-e147
pubmed: 34224543
Transpl Infect Dis. 2022 Feb;24(1):e13759
pubmed: 34787345
Nat Med. 2022 Mar;28(3):490-495
pubmed: 35046573
Transplantation. 2021 Jun 1;105(6):1365-1371
pubmed: 33988341
Lancet Infect Dis. 2022 May;22(5):622-635
pubmed: 34953520
Transpl Infect Dis. 2022 Apr;24(2):e13779
pubmed: 34932874
J Infect. 2022 Mar;84(3):e34-e35
pubmed: 35074507
Transplant Direct. 2022 Feb 10;8(3):e1292
pubmed: 35187216
Transplantation. 2022 Mar 1;106(3):436-446
pubmed: 34982758
N Engl J Med. 2021 Dec 2;385(23):e81
pubmed: 34587383
Nature. 2020 Aug;584(7821):430-436
pubmed: 32640463
NPJ Vaccines. 2021 May 13;6(1):74
pubmed: 33986272
Transpl Infect Dis. 2021 Oct;23(5):e13724
pubmed: 34534401
Nephrol Dial Transplant. 2021 Nov 9;36(11):2094-2105
pubmed: 34132811
Nat Rev Nephrol. 2021 Dec;17(12):785-787
pubmed: 34580488
Am J Transplant. 2022 Feb;22(2):640-645
pubmed: 34591350
N Engl J Med. 2021 Sep 23;385(13):1184-1195
pubmed: 34347950
Transpl Infect Dis. 2021 Oct;23(5):e13705
pubmed: 34324256
Science. 2022 Feb 25;375(6583):864-868
pubmed: 35076256

Auteurs

Guillaume Fernandes (G)

Division of Nephrology, Cliniques Universitaires Saint-Luc, Université Catholique de Louvain, Brussels, Belgium.

Arnaud Devresse (A)

Division of Nephrology, Cliniques Universitaires Saint-Luc, Université Catholique de Louvain, Brussels, Belgium.

Anais Scohy (A)

Microbiology, Cliniques Universitaires Saint-Luc, Université Catholique de Louvain, Brussels, Belgium.

Julien De Greef (J)

Internal Medicine and Infectious Disease, Cliniques Universitaires Saint-Luc, Université Catholique de Louvain, Brussels, Belgium.

Jean Cyr Yombi (JC)

Internal Medicine and Infectious Disease, Cliniques Universitaires Saint-Luc, Université Catholique de Louvain, Brussels, Belgium.

Leila Belkhir (L)

Internal Medicine and Infectious Disease, Cliniques Universitaires Saint-Luc, Université Catholique de Louvain, Brussels, Belgium.

Tom Darius (T)

Abdominal Surgery and Transplantation, Cliniques Universitaires Saint-Luc, Université Catholique de Louvain, Brussels, Belgium.

Michel Mourad (M)

Abdominal Surgery and Transplantation, Cliniques Universitaires Saint-Luc, Université Catholique de Louvain, Brussels, Belgium.

Antoine Buemi (A)

Abdominal Surgery and Transplantation, Cliniques Universitaires Saint-Luc, Université Catholique de Louvain, Brussels, Belgium.

Benoit Kabamba (B)

Microbiology, Cliniques Universitaires Saint-Luc, Université Catholique de Louvain, Brussels, Belgium.

Eric Goffin (E)

Division of Nephrology, Cliniques Universitaires Saint-Luc, Université Catholique de Louvain, Brussels, Belgium.

Nada Kanaan (N)

Division of Nephrology, Cliniques Universitaires Saint-Luc, Université Catholique de Louvain, Brussels, Belgium.

Classifications MeSH