Journalartikel

Humoral immunogenicity of COVID-19 vaccines in patients with inflammatory rheumatic diseases under treatment with Rituximab: a case-control study (COVID-19VacRTX)


AutorenlisteSchumacher, Falk; Mrdenovic, Nikola; Scheicht, Dennis; Pons-Kuehnemann, Joern; Scheibelhut, Christine; Strunk, Johannes

Jahr der Veröffentlichung2022

Seiten3912-3918

ZeitschriftRheumatology

Bandnummer61

Heftnummer10

ISSN1462-0324

eISSN1462-0332

Open Access StatusGreen

DOI Linkhttps://doi.org/10.1093/rheumatology/keac036

VerlagOxford University Press


Abstract
Objectives Patients with inflammatory rheumatic diseases (IRDs) treated with the anti-CD20 mAb rituximab (RTX) have been identified as high-risk for severe COVID-19 outcomes. Additionally, there is increased risk due to reduced humoral immune response, induced by therapeutic B cell depletion. This study sought to quantify humoral response after vaccination against SARS-CoV-2 in patients with IRD treated with RTX. It also sought to elucidate the influence of the time frame between the last RTX dose and the first vaccination, or the status of B cell depletion on antibody titre. Methods In this case-control study, patients with IRDs previously treated with RTX were examined for humoral immune response after completing the first series of vaccinations with approved vaccines [BNT162b2 (Biontech/Pfizer), RNA-1273 (Moderna), AZD1222 (AstraZeneca/Oxford), Ad26.COV2.S (Janssen/Johnson & Johnson)]. Antibody levels were quantified using the Euroimmun Anti-SARS-CoV-2 QuantiVac ELISA (EI-S1-IgG-quant). Blood samples were taken just before the next infusion with RTX after the vaccination. The interval between the last RTX infusion and the first vaccination against SARS-CoV-2 and other possible factors influencing the antibody levels were evaluated. Results A total of 102 patients were included. Of these, 65 (64%) showed a negative antibody level (<24 IU (international unit)/ml) after the vaccination. The comparative univariate analysis of the antibody levels achieved a significant result (P = 0.0008) for the time between the last RTX infusion and first vaccination against SARS-CoV-2. No CD19+ peripheral B-cells could be detected in 73 of the patients (72%). Conclusion The study confirms the negative impact of RTX on antibody level after vaccination against SARS-CoV-2. A clear relationship exists between the antibody titre and the interval between the last RTX infusion and the first vaccination, the number of peripheral B-cells, and immunoglobulin quantity. Improved understanding of the effect of these parameters can help guide synchronization of vaccination in relation to the RTX therapy regimen.



Autoren/Herausgeber




Zitierstile

Harvard-ZitierstilSchumacher, F., Mrdenovic, N., Scheicht, D., Pons-Kuehnemann, J., Scheibelhut, C. and Strunk, J. (2022) Humoral immunogenicity of COVID-19 vaccines in patients with inflammatory rheumatic diseases under treatment with Rituximab: a case-control study (COVID-19VacRTX), Rheumatology, 61(10), pp. 3912-3918. https://doi.org/10.1093/rheumatology/keac036

APA-ZitierstilSchumacher, F., Mrdenovic, N., Scheicht, D., Pons-Kuehnemann, J., Scheibelhut, C., & Strunk, J. (2022). Humoral immunogenicity of COVID-19 vaccines in patients with inflammatory rheumatic diseases under treatment with Rituximab: a case-control study (COVID-19VacRTX). Rheumatology. 61(10), 3912-3918. https://doi.org/10.1093/rheumatology/keac036



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ANCA-ASSOCIATED VASCULITISIMMUNOGENICITYRARITUXIMAB


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