"REAl LIfe" observational study on the effectiveness of Evusheld prophylaxis against SARS-CoV-2 omicron variants in vaccine non-responder immunocompromised patients (REALISE).

Antibodies COVID-19 Evusheld Immunocompromised patients Vaccination

Journal

Vaccine
ISSN: 1873-2518
Titre abrégé: Vaccine
Pays: Netherlands
ID NLM: 8406899

Informations de publication

Date de publication:
17 Aug 2024
Historique:
received: 17 03 2024
revised: 26 07 2024
accepted: 03 08 2024
medline: 19 8 2024
pubmed: 19 8 2024
entrez: 18 8 2024
Statut: aheadofprint

Résumé

Infection by SARS-CoV2 has become a challenge, especially for immunocompromised patients who show a weaker humoral response to COVID-19 vaccine. Tixagevimab+cilgavimab (Evusheld) is a combination of human monoclonal antibodies that can be used for pre-exposure prophylaxis to prevent infection or disease by SARS-CoV2. Our study aimed to investigate the effectiveness of Evusheld by comparing an Exposed and an Unexposed group. Immunocompromised patients were enrolled in the Evusheld Group between March and September 2022. All patients had anti-spike IgG antibody levels <260 BAU/ml before administration of Evusheld. Blood samples for serological evaluations were collected, and anti-Spike antibodies were tested. For the Unexposed Group, a serologic test was performed at enrollment and a questionnaire was performed after 6 months. 43 patients received Evusheld pre-exposure prophylaxis and 45 patients not receiving Evusheld were enrolled in the Unexposed group. The median age was 59.0 years in the Evusheld group, and 63.0 in the unexposed group. In the Evusheld group, during the Omicron wave in Italy, 23.3% of subjects developed symptomatic infection compared to 42.2% in the unexposed group. A majority of infections was seen in male respect to female patients. No difference in length of infection between the groups was seen. Antibody level remained higher than the basal threshold at 180 days from enrollment. Evusheld seems to reduce the rate of symptomatic infection in immunocompromised patients. Further data are required to determine whether this prophylaxis may have a longer-lasting effect over time.

Sections du résumé

BACKGROUND BACKGROUND
Infection by SARS-CoV2 has become a challenge, especially for immunocompromised patients who show a weaker humoral response to COVID-19 vaccine. Tixagevimab+cilgavimab (Evusheld) is a combination of human monoclonal antibodies that can be used for pre-exposure prophylaxis to prevent infection or disease by SARS-CoV2.
OBJECTIVES OBJECTIVE
Our study aimed to investigate the effectiveness of Evusheld by comparing an Exposed and an Unexposed group.
STUDY DESIGN METHODS
Immunocompromised patients were enrolled in the Evusheld Group between March and September 2022. All patients had anti-spike IgG antibody levels <260 BAU/ml before administration of Evusheld. Blood samples for serological evaluations were collected, and anti-Spike antibodies were tested. For the Unexposed Group, a serologic test was performed at enrollment and a questionnaire was performed after 6 months.
RESULTS RESULTS
43 patients received Evusheld pre-exposure prophylaxis and 45 patients not receiving Evusheld were enrolled in the Unexposed group. The median age was 59.0 years in the Evusheld group, and 63.0 in the unexposed group. In the Evusheld group, during the Omicron wave in Italy, 23.3% of subjects developed symptomatic infection compared to 42.2% in the unexposed group. A majority of infections was seen in male respect to female patients. No difference in length of infection between the groups was seen. Antibody level remained higher than the basal threshold at 180 days from enrollment.
CONCLUSIONS CONCLUSIONS
Evusheld seems to reduce the rate of symptomatic infection in immunocompromised patients. Further data are required to determine whether this prophylaxis may have a longer-lasting effect over time.

Identifiants

pubmed: 39154513
pii: S0264-410X(24)00890-9
doi: 10.1016/j.vaccine.2024.126208
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

126208

Informations de copyright

Copyright © 2024 The Authors. Published by Elsevier Ltd.. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Giuliana Lucia Esposito (GL)

Fondazione IRCCS Policlinico San Matteo, Microbiology and Virology Unit, Pavia, Italy,; Specialization School in Microbiology and Virology,University of Pavia, Pavia, Italy.. Electronic address: giulianalucia.esposito@universitadipavia.it.

Federico Fassio (F)

Department of Public Health, Experimental and Forensic Medicine, Section of Biostatistics and Clinical Epidemiology, University of Pavia, Pavia,Italy; Fondazione IRCCS Policlinico San Matteo, Medical direction, Pavia, Italy.

Daniela Girardi (D)

Department of Public Health, Experimental and Forensic Medicine, University of Pavia, Italy.; Fondazione IRCCS Policlinico San Matteo, Medical direction, Pavia, Italy.

Erica Picasso (E)

Fondazione IRCCS Policlinico San Matteo, Medical direction, Pavia, Italy.

Federica Meloni (F)

Fondazione IRCCS Policlinico San Matteo, UOS transplant center, Pavia, Italy.

Simone Montini (S)

Fondazione IRCCS Policlinico San Matteo, UOS transplant center, Pavia, Italy.

Veronica Codullo (V)

Fondazione IRCCS Policlinico San Matteo, Division of Rheumatology, Pavia, Italy.

Eleonora Francesca Pattonieri (EF)

Fondazione IRCCS Policlinico San Matteo, Division of Nephrology, Dialysis and Transplantation Pavia, Italy.

Irene Defrancesco (I)

Fondazione IRCCS Policlinico San Matteo, Division of Haematology, Pavia, Italy; Department of surgical, clinical, diagnostic and pediatric sciences, University of Pavia, Pavia, Italy.

Antonio Bianchessi (A)

Fondazione IRCCS Policlinico San Matteo, Division of Haematology, Pavia, Italy; Department of Molecular Medicine, University of Pavia, Pavia, Italy.

Monica Calvi (M)

Fondazione IRCCS Policlinico San Matteo, Pharmacy Unit, Pavia, Italy.

Elena Maria Seminari (EM)

Fondazione IRCCS Policlinico San Matteo, Infectious diseases division, Pavia, Italy.

Fausto Baldanti (F)

Fondazione IRCCS Policlinico San Matteo, Microbiology and Virology Unit, Pavia, Italy,; Department of surgical, clinical, diagnostic and pediatric sciences, University of Pavia, Pavia, Italy.

Daniele Lilleri (D)

Fondazione IRCCS Policlinico San Matteo, Microbiology and Virology Unit, Pavia, Italy.

Viola Novelli (V)

Fondazione IRCCS Policlinico San Matteo, Medical direction, Pavia, Italy.

Carlo Marena (C)

Fondazione IRCCS Policlinico San Matteo, Medical direction, Pavia, Italy.

Classifications MeSH