Humoral and cellular responses to SARS-CoV-2 in patients with B-cell haematological malignancies improve with successive vaccination |
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Authors: | Christopher L. Pinder Dylan Jankovic Thomas A. Fox Amy Kirkwood Louise Enfield Aljawharah Alrubayyi Emma Touizer Rosemarie Ford Rachael Pocock Jin-Sup Shin Joseph Ziegler Kirsty J. Thomson Kirit M. Ardeshna Dimitra Peppa Laura E. McCoy Emma C. Morris |
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Affiliation: | 1. Division of Infection and Immunity, University College London, London, UK;2. CR UK and UCL Cancer Trials Centre, UCL Cancer Institute, UCL, London, UK;3. Department of Clinical Haematology, University College London Hospitals, NHS Foundation Trust, London, UK;4. Division of Infection and Immunity, University College London, London, UK Department of Clinical Haematology, University College London Hospitals, NHS Foundation Trust, London, UK |
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Abstract: | Patients with haematological malignancies are more likely to have poor responses to vaccination. Here we provide detailed analysis of the humoral and cellular responses to COVID-19 vaccination in 69 patients with B-cell malignancies. Measurement of anti-spike IgG in serum demonstrated a low seroconversion rate with 27.1% and 46.8% of patients seroconverting after the first and second doses of vaccine, respectively. In vitro pseudoneutralisation assays demonstrated a poor neutralising response, with 12.5% and 29.5% of patients producing a measurable neutralising titre after the first and second doses, respectively. A third dose increased seropositivity to 54.3% and neutralisation to 51.5%, while a fourth dose further increased both seropositivity and neutralisation to 87.9%. Neutralisation titres post-fourth dose showed a positive correlation with the size of the B-cell population measured by flow cytometry, suggesting an improved response correlating with recovery of the B-cell compartment after B-cell depletion treatments. In contrast, interferon gamma ELISpot analysis showed a largely intact T-cell response, with the percentage of patients producing a measurable response boosted by the second dose to 75.5%. This response was maintained thereafter, with only a small increase following the third and fourth doses, irrespective of the serological response at these timepoints. |
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Keywords: | antibodies B cells haematological malignancies infection vaccines T cells |
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