Humoral and cellular responses to SARS‐CoV‐2 in patients with B‐cell haematological malignancies improve with successive vaccination

Author:

Pinder Christopher L.1ORCID,Jankovic Dylan1,Fox Thomas A.12ORCID,Kirkwood Amy3,Enfield Louise2,Alrubayyi Aljawharah1,Touizer Emma1,Ford Rosemarie1,Pocock Rachael2,Shin Jin‐Sup2,Ziegler Joseph2,Thomson Kirsty J.2,Ardeshna Kirit M.2,Peppa Dimitra1,McCoy Laura E.1ORCID,Morris Emma C.12

Affiliation:

1. Division of Infection and Immunity University College London London UK

2. Department of Clinical Haematology University College London Hospitals, NHS Foundation Trust London UK

3. CR UK and UCL Cancer Trials Centre UCL Cancer Institute, UCL London UK

Abstract

SummaryPatients 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.

Funder

University College London Hospitals NHS Foundation Trust

Medical Research Council

Publisher

Wiley

Subject

Hematology

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