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Antibody response following the third and fourth SARS-CoV-2 vaccine dose in individuals with common variable immunodeficiency.
Nielsen, Bibi Uhre; Drabe, Camilla Heldbjerg; Barnkob, Mike Bogetofte; Johansen, Isik Somuncu; Hansen, Anne Kirstine Kronborg; Nilsson, Anna Christine; Rasmussen, Line Dahlerup.
  • Nielsen BU; Department of Infectious Diseases, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark.
  • Drabe CH; Department of Infectious Diseases, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark.
  • Barnkob MB; Department of Clinical Immunology, Odense University Hospital, Odense, Denmark.
  • Johansen IS; Department of Infectious Diseases, Odense University Hospital, & Research Unit for Infectious Diseases, University of Southern Denmark, Odense, Denmark.
  • Hansen AKK; Department of Infectious Diseases, Odense University Hospital, & Research Unit for Infectious Diseases, University of Southern Denmark, Odense, Denmark.
  • Nilsson AC; Department of Clinical Immunology, Odense University Hospital, Odense, Denmark.
  • Rasmussen LD; Department of Infectious Diseases, Odense University Hospital, & Research Unit for Infectious Diseases, University of Southern Denmark, Odense, Denmark.
Front Immunol ; 13: 934476, 2022.
Article in English | MEDLINE | ID: covidwho-2141953
ABSTRACT

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.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Viral Vaccines / Common Variable Immunodeficiency / COVID-19 Type of study: Observational study / Prognostic study Topics: Vaccines Limits: Humans Language: English Journal: Front Immunol Year: 2022 Document Type: Article Affiliation country: Fimmu.2022.934476

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Viral Vaccines / Common Variable Immunodeficiency / COVID-19 Type of study: Observational study / Prognostic study Topics: Vaccines Limits: Humans Language: English Journal: Front Immunol Year: 2022 Document Type: Article Affiliation country: Fimmu.2022.934476