Real World Use of Tixagevimab/Cilgavimab Pre-Exposure Prophylaxis of COVID-19 in Immunocompromised Individuals: Data from the OCTOPUS Study.

Real World Use of Tixagevimab/Cilgavimab Pre-Exposure Prophylaxis of COVID-19 in Immunocompromised Individuals: Data from the OCTOPUS Study.

Publication date: Jul 17, 2024

Objective. We aimed to report the real-world use and outcomes over time in immunocompromised individuals receiving tixagevimab/cilgavimab (T/C) pre-exposure prophylaxis (PrEP). Methods. This observational study included participants who received T/C PrEP, categorized into three groups: (i) No COVID-19 (NoC), i. e., participants who never had COVID-19; (ii) Hybrids (H), i. e., participants who had COVID-19 before PrEP; and (iii) Break-through Infections (BTIs), i. e., participants who had COVID-19 after PrEP. The study measured several immune markers at the administration of T/C (T0) at 3 (T1), 6 (T2), and 9 (T3) months afterward. These markers included: anti-receptor-binding domain (RBD) IgG antibodies; BA. 5-neutralizing antibodies (nAbs); mucosal IgG; and T cell immunity. The incidence rate ratios for BTIs were analyzed using a Poisson regression model. Results. A total of 231 participants with a median age of 63 years (IQR 54. 0-73. 0). were included. Among these, 84% had hematological diseases and received a median of three vaccine doses. N = 72 participants belonged to the NoC group, N = 103 to the H group, and n = 56 to the BTI group (24%), with most BTIs being mild/moderate. The incidence rate (IR) of BTIs was 4. 2 per 100 patient-months (95% CI 3. 2-5. 4), with no associated risk factors identified. There was a significant increase in anti-RBD IgG levels 3 months after the T/C administration in all groups, followed by a decline at 6 months, whereas at the same time points, geometric mean titers (GMTs) of anti-BA. 5 nAbs were low for all groups and were around or below the detection threshold. No significant changes were observed in IFN-γ levels. The mucosal immune response was observed only 3 months after the PrEP administration. Conclusion. We provided a real-world experience model on the clinical efficacy of T/C PrEP in preventing severe COVID-19 during the Omicron wave through a comprehensive virological and immunological study. While waiting for the arrival of new monoclonal antibodies that can effectively neutralize the most recent variants, T/C PrEP remains the only viable strategy in the available armamentarium today to prevent COVID-19 complications in an extremely fragile population with suboptimal immune responses to COVID-19 vaccines.

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Concepts Keywords
Armamentarium cell mediated immunity
Covid humoral immunity
Immunocompromised passive pre-prophylaxis
Months SARS coronavirus
Octopus

Semantics

Type Source Name
disease MESH COVID-19
disease VO report
disease VO time
disease MESH Infections
disease IDO cell
disease MESH hematological diseases
disease VO vaccine
disease VO mucosal immune response
disease VO viable
drug DRUGBANK Nonoxynol-9
disease MESH complications
disease VO population
disease MESH Infectious Diseases
drug DRUGBANK L-Aspartic Acid
disease MESH Emerging Infectious Diseases
drug DRUGBANK Coenzyme M
disease MESH seroconversion
disease VO effectiveness
disease MESH death
disease MESH hematological malignancies
disease VO organ
disease MESH breakthrough infections
disease MESH emergency
disease VO effective
drug DRUGBANK Oxygen
disease IDO infection
disease VO regulatory agency
disease VO protocol
disease IDO blood
disease VO immunization
disease VO vaccinated
disease VO USA
disease IDO assay
disease MESH drooling
drug DRUGBANK Indoleacetic acid
disease IDO production
disease MESH non Hodgkin lymphoma
disease MESH multiple myeloma
disease MESH chronic lymphocytic leukemia
disease MESH multiple sclerosis
disease MESH comorbidity
disease MESH COPD
disease VO age
disease MESH Hypertension
disease MESH Cardiovascular Disease
disease MESH Dyslipidemia
disease MESH cancer
disease VO titer

Original Article

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