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SHR Neuro Cancer Cardio Lipid Metab Microb

Schulz, E; Hodl, I; Forstner, P; Hatzl, S; Sareban, N; Moritz, M; Fessler, J; Dreo, B; Uhl, B; Url, C; Grisold, AJ; Khalil, M; Kleinhappl, B; Enzinger, C; Stradner, MH; Greinix, HT; Schlenke, P; Steinmetz, I.
CD19+IgD+CD27- Naïve B Cells as Predictors of Humoral Response to COVID 19 mRNA Vaccination in Immunocompromised Patients.
Front Immunol. 2021; 12:803742 Doi: 10.3389/fimmu.2021.803742 [OPEN ACCESS]
Web of Science PubMed PUBMED Central FullText FullText_MUG

 

Leading authors Med Uni Graz
Hodl Isabel
Schulz Eduard
Stradner Martin Helmut
Co-authors Med Uni Graz
Dreo Barbara
Enzinger Christian
Fessler Johannes
Forstner Patrick
Greinix Hildegard
Grisold Andrea
Hatzl Stefan
Khalil Michael
Kleinhappl Barbara
Moritz Martina
Sareban Nazanin
Schlenke Peter
Steinmetz Ivo
Uhl Barbara
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Abstract:
Immunocompromised patients are considered high-risk and prioritized for vaccination against COVID-19. We aimed to analyze B-cell subsets in these patients to identify potential predictors of humoral vaccination response. Patients (n=120) suffering from hematologic malignancies or other causes of immunodeficiency and healthy controls (n=79) received a full vaccination series with an mRNA vaccine. B-cell subsets were analyzed prior to vaccination. Two independent anti-SARS-CoV-2 immunoassays targeting the receptor-binding domain (RBD) or trimeric S protein (TSP) were performed three to four weeks after the second vaccination. Seroconversion occurred in 100% of healthy controls, in contrast to 67% (RBD) and 82% (TSP) of immunocompromised patients, while only 32% (RBD) and 22% (TSP) achieved antibody levels comparable to those of healthy controls. The number of circulating CD19+IgD+CD27- naïve B cells was strongly associated with antibody levels (ρ=0.761, P<0.001) and the only independent predictor for achieving antibody levels comparable to healthy controls (OR 1.07 per 10-µL increase, 95%CI 1.02-1.12, P=0.009). Receiver operating characteristic analysis identified a cut-off at ≥61 naïve B cells per µl to discriminate between patients with and without an optimal antibody response. Consequently, measuring of naïve B cells in immunocompromised hematologic patients could be useful in predicting their humoral vaccination response.
Find related publications in this database (using NLM MeSH Indexing)
Adult - administration & dosage
Aged - administration & dosage
Antibodies, Neutralizing - immunology
Antibodies, Viral - immunology
B-Lymphocyte Subsets - immunology
COVID-19 - prevention & control
COVID-19 Vaccines - immunology
Female - administration & dosage
Humans - administration & dosage
Immunocompromised Host - immunology
Immunogenicity, Vaccine - immunology
Male - administration & dosage
Middle Aged - administration & dosage
SARS-CoV-2 - administration & dosage
Vaccines, Synthetic - immunology
mRNA Vaccines - immunology

Find related publications in this database (Keywords)
mRNA vaccine
COVID-19
B cells
cancer
immunodeficiencies
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