Humoral Immune Responses after an Omicron-Adapted Booster BNT162b2 Vaccination in Patients with Lymphoid Malignancies
Line Dam Heftdal, Cecilie Bo Hansen, Sebastian Rask Hamm, Laura Pérez-Alós, Kamille Fogh, Mia Pries-Heje, Rasmus Bo Hasselbalch, Dina Leth Møller, Anne Ortved Gang, Sisse Rye Ostrowski, Ruth Frikke-Schmidt, Erik Sørensen, Linda Hilsted, Henning Bundgaard, Peter Garred

TL;DR
This study shows that patients with lymphoid malignancies had improved antibody responses after receiving an Omicron-adapted booster vaccine, regardless of the specific variant included.
Contribution
The study provides evidence that Omicron-adapted booster vaccines can boost immune responses in immunocompromised patients with lymphoid malignancies.
Findings
Antibody concentrations increased by 0.09 log10 AU/mL/month after Omicron-adapted vaccination.
Neutralizing capacity increased by 0.9 percent points/month in patients with lymphoid malignancies.
The increase in immune response was not associated with the specific Omicron variant in the vaccine.
Abstract
To accommodate waning COVID-19 vaccine immunity to emerging SARS-CoV-2 variants, variant-adapted mRNA vaccines have been introduced. Here, we examine serological responses to the BA.1 and BA.4-5 Omicron variant-adapted BNT162b2 COVID-19 vaccines in people with lymphoid malignancies. We included 233 patients with lymphoid malignancies (chronic lymphocytic B-cell leukemia: 73 (31.3%), lymphoma: 89 (38.2%), multiple myeloma/amyloidosis: 71 (30.5%)), who received an Omicron-adapted mRNA-based COVID-19 vaccine. IgG and neutralizing antibodies specific for the receptor-binding domain (RBD) of SARS-CoV-2 were measured using ELISA-based methods. Differences in antibody concentrations and neutralizing capacity and associations with risk factors were assessed using mixed-effects models. Over the period of vaccination with an Omicron-adapted COVID-19 vaccine, the predicted mean concentration of…
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Taxonomy
TopicsSARS-CoV-2 and COVID-19 Research · Immunotherapy and Immune Responses · CAR-T cell therapy research
