Real world use of Tixagevimab/Cilgavimab pre-exposure prophylaxis of COVID-19 in immunocompromised individuals: data from the OCTOPUS study.

Alessandra Vergori,Giulia Matusali,Eleonora Cimini,Licia Bordi,Paola Borrelli,Simone Lanini, Roberta Palazzi, Jessica Paulicelli,Davide Mariotti,Valentina Mazzotta,Stefania Notari, R. Casetti,Massimo Francalancia,Silvia Rosati, Alessandra D’Abramo, Cosmina Mija,Paola Mencarini, Eugenia Milozzi, Caraffa E, Simona Sica,Elisabetta Metafuni,Federica Sorà, Angela Rago, Agostina Siniscalchi, Elisabetta Abruzzese,Mariagrazia Garzia, Giovanni Luzi,Roberta Battistini, Luca Prosperini,Antonella Cingolani,Enrico Girardi,Fabrizio Maggi,Andrea Antinori

crossref(2024)

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摘要
We report real world use over time in immunocompromised subjects receiving tixagevimab/cilgavimab (T/C) pre-exposure prophylaxis (PrEP). Observational study on participants receiving T/C PrEP stratified: never had COVID-19 (NoC), hybrids (H) and breakthrough infections (BTIs) if COVID-19 before or after PrEP, respectively. Anti-RBD IgG and BA.5 neutralizing antibodies (nAbs), mucosal IgG, T-cell immunity at the administration of T/C (T0), 3 (T1), 6 (T2), and 9 (T3) months after, were measured. Comparison of markers in each group across timepoints, Poisson regression model for BTIs incidence rate ratios were performed. N=231 participants: median age 63 years (IQR 54.0-73.0), 84% hematological disease, median vaccine dose of three. N=72 NoC, 103 H and 56 (24%) BTIs, mostly mild/moderate, IR 4.2 (95%CI 3.2-5.4) BTIs/100 patients-months, no factors associated with. A significant increase of anti-RBD IgG at T1 was observed in all the groups, with a decline at T2. GMTs of anti-BA.5 nAbs were low at T1 for all the groups and around/below the cut off. No changes of IFN-γ. Overall, a mucosal response was observed at T1. An incidence of 24% of mild/moderate BTIs was observed. Anti-RBD IgG levels persistence was ensured, BA.5 nAbs were low/undetectable, cellular T immunity remained stable.
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