Vergori Alessandra, Matusali Giulia, Cimini Eleonora, Bordi Licia, Borrelli Paola, Lanini Simone, Palazzi Roberta, Paulicelli Jessica, Mariotti Davide, Mazzotta Valentina, Notari Stefania, Casetti Rita, Francalancia Massimo, Rosati Silvia, D'Abramo Alessandra, Mija Cosmina, Mencarini Paola, Milozzi Eugenia, Caraffa Emanuela, Sica Simona, Metafuni Elisabetta, Sorà Federica, Rago Angela, Siniscalchi Agostina, Abruzzese Elisabetta, Garzia Mariagrazia, Luzi Giovanni, Battistini Roberta, Prosperini Luca, Cingolani Antonella, Girardi Enrico, Maggi Fabrizio, Antinori Andrea
Viral Immunodeficiencies Unit, National Institute for Infectious Diseases "L. Spallanzani", Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS), 00149 Rome, Italy.
Laboratory of Virology, National Institute for Infectious Diseases "L. Spallanzani", Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS), 00149 Rome, Italy.
Vaccines (Basel). 2024 Jul 17;12(7):784. doi: 10.3390/vaccines12070784.
. We aimed to report the real-world use and outcomes over time in immunocompromised individuals receiving tixagevimab/cilgavimab (T/C) pre-exposure prophylaxis (PrEP). . 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. . 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. . 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.
我们旨在报告接受替沙格韦单抗/西加韦单抗(T/C)暴露前预防(PrEP)的免疫功能低下个体随着时间推移的实际使用情况和结果。这项观察性研究纳入了接受T/C PrEP的参与者,分为三组:(i)未感染新冠病毒(NoC),即从未感染过新冠病毒的参与者;(ii)混合组(H),即PrEP前感染过新冠病毒的参与者;(iii)突破性感染(BTI)组,即PrEP后感染过新冠病毒的参与者。该研究在给予T/C时(T0)、之后3个月(T1)、6个月(T2)和9个月(T3)测量了几种免疫标志物。这些标志物包括:抗受体结合域(RBD)IgG抗体;BA.5中和抗体(nAbs);黏膜IgG;以及T细胞免疫。使用泊松回归模型分析BTI的发病率比。总共纳入了231名参与者,中位年龄为63岁(四分位间距54.0 - 73.0)。其中,84%患有血液系统疾病,接受的疫苗剂量中位数为3剂。NoC组有72名参与者,H组有103名,BTI组有56名(24%),大多数BTI为轻度/中度。BTI的发病率(IR)为每100患者月4.2例(95%置信区间3.2 - 5.4),未发现相关危险因素。所有组在给予T/C后3个月抗RBD IgG水平显著升高,随后在6个月下降,而在相同时间点,所有组抗BA.5 nAbs的几何平均滴度(GMT)较低,且在检测阈值左右或以下。IFN - γ水平未观察到显著变化。仅在PrEP给药后3个月观察到黏膜免疫反应。我们通过全面的病毒学和免疫学研究,提供了一个关于T/C PrEP在奥密克戎毒株流行期间预防重症新冠病毒感染临床疗效的真实世界经验模型。在等待能够有效中和最新变体的新型单克隆抗体到来之际,T/C PrEP仍然是当今可用手段中唯一可行的策略,用于在对新冠病毒疫苗免疫反应欠佳的极其脆弱人群中预防新冠病毒感染并发症。