Immunogenicity and safety of a third and subsequent COVID-19 vaccine doses in patients with plasma cell dyscrasias

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Authors: Sita Bhella, Gerard Agbayani, Katrina Hueniken, Abi Vijenthira, Allison M. Wilkin, Michaël Sébag, Peng Wang, Lisa K. Hicks, Annette E. Hay, Seyed Mohammadmehdi Hosseini-Moghaddam, Sarit E. Assouline, Amaris Karin Balitsky
+33 more Graeme Fraser, Joy E. Mangel, Carolyn Owen, Tony Reiman, Laurie Helen Sehn, Heather J. Sutherland, Corey R. Arnold, Arleigh B. Robertson McCurdy, Donna Ellen Reece, Tamara Leite, Erinn McCarthy, Curtis Cooper, Angela M. Crawley, Marc‐André Langlois, C. Arianne Buchan, David Allan, Andrew Aw, Stephen Betschel, Shelly Bolotin, Joseph M. Brandwein, Christopher Bredeson, James Brooks, Matthew Cheung, Michael Patvin Chu, Vikas Gupta, Natasha K. Kekre, Deepali Kumar, Caroline Moltzan, Anca A. Prica, Julie Stakiw, Alissa Wright, Tara Baetz, Jill J. Dudebout
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References: 34

Abstract

ABSTRACT: Plasma cell dyscrasias (PCD) are a group of hematologic disorders associated with immune dysfunction from underlying disease and/or treatment. With the continued circulation of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), optimizing and maintaining durable protection in this vulnerable population through vaccination remains important. A prospective cohort study was conducted between August 2021 and January 2023 across 12 sites in Canada to evaluate humoral immunity to COVID-19 vaccination in participants with hematologic malignancies. Participants were monitored longitudinally, and finger-prick dried blood spot cards were obtained at specific intervals based on vaccination. Serum antibodies against SARS-CoV-2 proteins after the third, fourth, and fifth dose were measured by high-throughput enzyme-linked immunosorbent assay. Differences in antispike (anti-S) seropositivity by vaccine dose number and clinical risk factors were analyzed by logistic regression. A total of 262 unique participants with 983 samples were included for analysis, among which 66% were diagnosed with PCD. Analysis of the predicted probability of immunity showed consistently higher proportions of participants with PCD with vaccine (anti-S) immunity compared with those with infection-derived (antinucleocapsid) immunity throughout the study. Although vaccine responses appeared to wane 6 months after dose 3 and, to a lesser extent, after dose 4, subsequent doses cumulatively increased anti-S immunity. Seropositivity decreased with anti-CD38 therapy and older age, although the receipt of additional vaccine doses significantly improved anti-S immunity. Overall, this study demonstrated that the third and subsequent COVID-19 vaccine doses could safely improve humoral immunity in participants with PCD. Although anti-CD38 therapy and age reduced seropositivity, antibody responses could still be enhanced with vaccine doses beyond the primary 3-dose series.

Fields of Study & Subjects

SARS-CoV-2 and COVID-19 Research Vaccine Coverage and Hesitancy COVID-19 Clinical Research Studies

Publication details

Journal / source
Blood Advances
Volume
10
Issue
9
Pages
2890–2903
Publication date
27 January 2026
Language
EN