SARS-CoV-2 pre-exposure prophylaxis with tixagevimab/cilgavimab (AZD7442) provides protection in inborn errors of immunity with antibody defects: a real-world experience

被引:0
作者
Pulvirenti, Federica [1 ]
Garzi, Giulia [2 ]
Milito, Cinzia [2 ]
Sculco, Eleonora [2 ]
Sciannamea, Maddalena [2 ]
Napoli, Anna [2 ,3 ]
Cinti, Lilia [2 ,3 ]
Roberto, Piergiorgio [3 ]
Punziano, Alessandra [4 ]
Carrabba, Maria [5 ]
Piano Mortari, Eva [2 ,6 ]
Carsetti, Rita [6 ]
Antonelli, Guido [2 ,3 ]
Quinti, Isabella [1 ,2 ]
机构
[1] Sapienza Univ Hosp, Reference Ctr Primary Immune Deficiencies, Policlin Umberto I, Rome, Italy
[2] Sapienza Univ, Dept Mol Med, Rome, Italy
[3] Sapienza Univ Hosp, Microbiol & Virol Unit, Policlin Umberto I, Rome, Italy
[4] Univ Naples Federico II, Dept Translat Med Sci, Naples, Italy
[5] Fdn IRCCS Ca Granda Osped Maggiore Policlin, Internal Med Dept, Geriatr Unit, Milan, Italy
[6] Ist Ricovero & Cura Carattere Sci IRCCS, Bambino Gesu Childrens Hosp, Cell Unit B, Immunol Res Area, Rome, Italy
来源
FRONTIERS IN IMMUNOLOGY | 2023年 / 14卷
关键词
SARS-CoV-2; COVID-19; inborn errors of immunity; immunoglobulin replacement (IgRT); monoclonal antibody; tixagevimab/cilgavimab prophylaxis; common variable immune deficiency (CVID);
D O I
10.3389/fimmu.2023.1249462
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background: Preventive strategies against severe COVID-19 in Inborn Errors of Immunity (IEI) include bivalent vaccines, treatment with SARS-CoV-2 monoclonal antibodies (mAbs), early antiviral therapies, and pre-exposure prophylaxis (PrEP).Objective: To assess the effectiveness of the PrEP with tixagevimab/cilgavimab (AZD7442) in IEI with primary antibody defects during the COVID-19 Omicron wave.Methods A six-month prospective study evaluated the SARS-CoV-2 infection rate and the COVID-19 severity in the AZD7442 group, in the no-AZD7442 group, and in a group of patients with a recent SARS-CoV-2 infection (< three months). Spike-specific IgG levels were measured at regular intervals.Results: Six out of thirty-three patients (18%) and 54/170 patients (32%) became infected in the AZD7442 group and in the no-AZD7442 group, respectively. Within 90 days post-administration, the AZD7442 group was 85% less likely to be infected and 82% less likely to have a symptomatic disease than the no-AZD7442 group. This effect was lost thereafter. In the entire cohort, no mortality/hospitalisation was observed. The control group of 35 recently infected patients was 88% and 92% less likely to be infected than the AZD7442 and no-AZD7442 groups. Serum anti-Spike IgG reached the highest peak seven days post-AZD7442 PrEP then decreased, remaining over 1000 BAU/mL 180 days thereafter.Conclusion: In patients with IEI and antibody defects, AZD7442 prophylaxis had a transient protective effect, possibly lost possibly because of the appearance of new variants. However, PrEP with newer mAbs might still represent a feasible preventive strategy in the future in this population.
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