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Antibody response following the third and fourth SARS-CoV-2 vaccine dose in individuals with common variable immunodeficiency

BACKGROUND: The antibody response after vaccination is impaired in common variable immunodeficiency (CVID). OBJECTIVE: We aimed to study the spike receptor-binding domain IgG antibody (anti-S-RBD) levels during a four-dose SARS-CoV-2 vaccination strategy and after monoclonal antibody (mAB) treatment...

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Detalles Bibliográficos
Autores principales: Nielsen, Bibi Uhre, Drabe, Camilla Heldbjerg, Barnkob, Mike Bogetofte, Johansen, Isik Somuncu, Hansen, Anne Kirstine Kronborg, Nilsson, Anna Christine, Rasmussen, Line Dahlerup
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9366053/
https://www.ncbi.nlm.nih.gov/pubmed/35967433
http://dx.doi.org/10.3389/fimmu.2022.934476
Descripción
Sumario:BACKGROUND: The antibody response after vaccination is impaired in common variable immunodeficiency (CVID). OBJECTIVE: We aimed to study the spike receptor-binding domain IgG antibody (anti-S-RBD) levels during a four-dose SARS-CoV-2 vaccination strategy and after monoclonal antibody (mAB) treatment in CVID. Moreover, we assessed the anti-S-RBD levels in immunoglobulin replacement therapy (IgRT) products. METHODS: In an observational study, we examined anti-S-RBD levels after the second, third, and fourth dose of mRNA SARS-CoV-2 vaccines. Moreover, we measured anti-S-RBD after treatment with mAB. Finally, anti-S-RBD was assessed in common IgRT products. Antibody non-responders (anti-S-RBD < 7.1) were compared by McNemar’s test and anti-S-RBD levels were compared with paired and non-paired Wilcoxon signed rank tests as well as Kruskal–Wallis tests. RESULTS: Among 33 individuals with CVID, anti-S-RBD levels increased after the third vaccine dose (165 BAU/ml [95% confidence interval: 85; 2280 BAU/ml], p = 0.006) and tended to increase after the fourth dose (193 BAU/ml, [−22; 569 BAU/ml], p = 0.080) compared to the previous dose. With increasing number of vaccinations, the proportion of patients who seroconverted (anti-S-RBD ≥ 7.1) increased non-significantly. mAB treatment resulted in a large increase in anti-S-RBD and a higher median level than gained after the fourth dose of vaccine (p = 0.009). IgRT products had varying concentrations of anti-S-RBD (p < 0.001), but none of the products seemed to affect the overall antibody levels (p = 0.460). CONCLUSION: Multiple SARS-CoV-2 vaccine doses in CVID seem to provide additional protection, as antibody levels increased after the third and fourth vaccine dose. However, anti-S-RBD levels from mAB outperform the levels mounted after vaccination. CLINICAL IMPLICATIONS: Boosting with SARS-CoV-2 vaccines seems to improve the antibody response in CVID patients. CAPSULE SUMMARY: The third and possibly also the fourth dose of mRNA SARS-CoV-2 vaccine in CVID improve the antibody response as well as stimulate seroconversion in most non-responders.