» Articles » PMID: 36642057

Improvement of Humoral Immunity by Repeated Dose-intensified COVID-19 Vaccinations in Primary Non- to Low-responders and B Cell Deficient Rheumatic Disease Patients

Abstract

Objective: To determine whether repeated, dose-intensified mRNA vaccinations against COVID-19 increase humoral immunity in previously low-responding patients with autoimmune rheumatic diseases (AIRD), including rituximab-treated and B cell depleted patients.

Methods: Of 308 AIRD patients receiving basic immunization, 98 had a low serological response against SARS-CoV-2 with a neutralizing capacity of < 70% using surrogate neutralization assay. 38 patients received a third vaccination with 30 μg BNT162b2 16 weeks after second vaccination. If neutralizing serum capacity was below 70% four weeks after the last vaccination, then the fourth vaccination (n = 19) and the fifth (n = 4) vaccination with 100 μg mRNA-1273 took place eight weeks after the last vaccination.

Results: Each of the three booster vaccinations resulted in a significant increase of mean serum neutralizing capacity (3rd: Δ = 42%, p < 0.001; 4th: Δ = 19%, p = 0.049 and 5th: Δ = 51%, p = 0.043) and produced a significant proportion of high-responders (3rd: 34%; 4th: 32% and 5th: 75%). Low B cell counts (p = 0.047), lower previous antibody response (p < 0.001) and rituximab therapy (p = 0.021) were negatively associated with successful response to the third but not to the fourth vaccination. Remarkably, substantial increases in neutralization capacity of up to 99% were observed after repeated vaccinations in B cell depleted patients.

Conclusion: AIRD patients with low humoral response benefited from up to three repeated dose-intensified mRNA booster vaccinations - despite low B cell count and previous rituximab therapy. Each additional vaccination substantially reduced the number of low-responding, vulnerable patients.

Citing Articles

Safety, efficacy, and immunogenicity of SARS-CoV-2 mRNA vaccination in children and adult patients with rheumatic diseases: a comprehensive literature review.

Dhanasekaran P, Karasu B, Mak A Rheumatol Int. 2024; 44(12):2757-2794.

PMID: 39576327 DOI: 10.1007/s00296-024-05734-x.


Effect of DMARDs on the immunogenicity of vaccines.

van Sleen Y, van der Geest K, Huckriede A, van Baarle D, Brouwer E Nat Rev Rheumatol. 2023; 19(9):560-575.

PMID: 37438402 DOI: 10.1038/s41584-023-00992-8.

References
1.
Arumahandi de Silva A, Frommert L, Albach F, Klotsche J, Scholz V, Jeworowski L . Pausing methotrexate improves immunogenicity of COVID-19 vaccination in elderly patients with rheumatic diseases. Ann Rheum Dis. 2022; 81(6):881-888. PMC: 9120396. DOI: 10.1136/annrheumdis-2021-221876. View

2.
Schulze-Koops H, Krueger K, Vallbracht I, Hasseli R, Skapenko A . Increased risk for severe COVID-19 in patients with inflammatory rheumatic diseases treated with rituximab. Ann Rheum Dis. 2020; 80(5):e67. DOI: 10.1136/annrheumdis-2020-218075. View

3.
Glaesener S, Quach T, Onken N, Weller-Heinemann F, Dressler F, Huppertz H . Distinct effects of methotrexate and etanercept on the B cell compartment in patients with juvenile idiopathic arthritis. Arthritis Rheumatol. 2014; 66(9):2590-600. PMC: 4288311. DOI: 10.1002/art.38736. View

4.
Arnold J, Winthrop K, Emery P . COVID-19 vaccination and antirheumatic therapy. Rheumatology (Oxford). 2021; 60(8):3496-3502. PMC: 7989162. DOI: 10.1093/rheumatology/keab223. View

5.
Loarce-Martos J, Garcia-Fernandez A, Lopez-Gutierrez F, Garcia-Garcia V, Calvo-Sanz L, Del Bosque-Granero I . High rates of severe disease and death due to SARS-CoV-2 infection in rheumatic disease patients treated with rituximab: a descriptive study. Rheumatol Int. 2020; 40(12):2015-2021. PMC: 7499013. DOI: 10.1007/s00296-020-04699-x. View