Fourth mRNA COVID-19 vaccination in immunocompromised patients with haematological malignancies (COBRA KAI): a cohort study.
Antibody response
Booster vaccination
COVID-19 vaccination
Haematological malignancies
Immunocompromised
SARS-CoV-2
Journal
EClinicalMedicine
ISSN: 2589-5370
Titre abrégé: EClinicalMedicine
Pays: England
ID NLM: 101733727
Informations de publication
Date de publication:
Jul 2023
Jul 2023
Historique:
received:
01
03
2023
revised:
15
05
2023
accepted:
25
05
2023
medline:
20
6
2023
pubmed:
20
6
2023
entrez:
20
6
2023
Statut:
ppublish
Résumé
Patients with haematological malignancies have impaired antibody responses to SARS-CoV-2 vaccination. We aimed to investigate whether a fourth mRNA COVID-19 vaccination improved antibody quantity and quality. In this cohort study, conducted at 5 sites in the Netherlands, we compared antibody concentrations 28 days after 4 mRNA vaccinations (3-dose primary series plus 1 booster vaccination) in SARS-CoV-2 naive, immunocompromised patients with haematological malignancies to those obtained by age-matched, healthy individuals who had received the standard primary 2-dose mRNA vaccination schedule followed by a first booster mRNA vaccination. Prior to and 4 weeks after each vaccination, peripheral blood samples and data on demographic parameters and medical history were collected. Concentrations of antibodies that bind spike 1 (S1) and nucleocapsid (N) protein of SARS-CoV-2 were quantified in binding antibody units (BAU) per mL according to the WHO International Standard for COVID-19 serological tests. Seroconversion was defined as an S1 IgG concentration >10 BAU/mL and a previous SARS-CoV-2 infection as N IgG >14.3 BAU/mL. Antibody neutralising activity was tested using lentiviral-based pseudoviruses expressing spike protein of SARS-CoV-2 wild-type (D614G), Omicron BA.1, and Omicron BA.4/5 variants. This study is registered with EudraCT, number 2021-001072-41. Between March 24, 2021 and May 4, 2021, 723 patients with haematological diseases were enrolled, of which 414 fulfilled the inclusion criteria for the current analysis. Although S1 IgG concentrations in patients significantly improved after the fourth dose, they remained significantly lower compared to those obtained by 58 age-matched healthy individuals after their first booster (third) vaccination. The rise in neutralising antibody concentration was most prominent in patients with a recovering B cell compartment, although potent responses were also observed in patients with persistent immunodeficiencies. 19% of patients never seroconverted, despite 4 vaccinations. Patients who received their first 2 vaccinations when they were B cell depleted and the third and fourth vaccination during B cell recovery demonstrated similar antibody induction dynamics as patients with normal B cell numbers during the first 2 vaccinations. However, the neutralising capacity of these antibodies was significantly better than that of patients with normal B cell numbers after two vaccinations. A fourth mRNA COVID-19 vaccination improved S1 IgG concentrations in the majority of patients with a haematological malignancy. Vaccination during B cell depletion may pave the way for better quality of antibody responses after B cell reconstitution. The Netherlands Organisation for Health Research and Development and Amsterdam UMC.
Sections du résumé
Background
UNASSIGNED
Patients with haematological malignancies have impaired antibody responses to SARS-CoV-2 vaccination. We aimed to investigate whether a fourth mRNA COVID-19 vaccination improved antibody quantity and quality.
Methods
UNASSIGNED
In this cohort study, conducted at 5 sites in the Netherlands, we compared antibody concentrations 28 days after 4 mRNA vaccinations (3-dose primary series plus 1 booster vaccination) in SARS-CoV-2 naive, immunocompromised patients with haematological malignancies to those obtained by age-matched, healthy individuals who had received the standard primary 2-dose mRNA vaccination schedule followed by a first booster mRNA vaccination. Prior to and 4 weeks after each vaccination, peripheral blood samples and data on demographic parameters and medical history were collected. Concentrations of antibodies that bind spike 1 (S1) and nucleocapsid (N) protein of SARS-CoV-2 were quantified in binding antibody units (BAU) per mL according to the WHO International Standard for COVID-19 serological tests. Seroconversion was defined as an S1 IgG concentration >10 BAU/mL and a previous SARS-CoV-2 infection as N IgG >14.3 BAU/mL. Antibody neutralising activity was tested using lentiviral-based pseudoviruses expressing spike protein of SARS-CoV-2 wild-type (D614G), Omicron BA.1, and Omicron BA.4/5 variants. This study is registered with EudraCT, number 2021-001072-41.
Findings
UNASSIGNED
Between March 24, 2021 and May 4, 2021, 723 patients with haematological diseases were enrolled, of which 414 fulfilled the inclusion criteria for the current analysis. Although S1 IgG concentrations in patients significantly improved after the fourth dose, they remained significantly lower compared to those obtained by 58 age-matched healthy individuals after their first booster (third) vaccination. The rise in neutralising antibody concentration was most prominent in patients with a recovering B cell compartment, although potent responses were also observed in patients with persistent immunodeficiencies. 19% of patients never seroconverted, despite 4 vaccinations. Patients who received their first 2 vaccinations when they were B cell depleted and the third and fourth vaccination during B cell recovery demonstrated similar antibody induction dynamics as patients with normal B cell numbers during the first 2 vaccinations. However, the neutralising capacity of these antibodies was significantly better than that of patients with normal B cell numbers after two vaccinations.
Interpretation
UNASSIGNED
A fourth mRNA COVID-19 vaccination improved S1 IgG concentrations in the majority of patients with a haematological malignancy. Vaccination during B cell depletion may pave the way for better quality of antibody responses after B cell reconstitution.
Funding
UNASSIGNED
The Netherlands Organisation for Health Research and Development and Amsterdam UMC.
Identifiants
pubmed: 37337616
doi: 10.1016/j.eclinm.2023.102040
pii: S2589-5370(23)00217-1
pmc: PMC10270678
doi:
Types de publication
Journal Article
Langues
eng
Pagination
102040Investigateurs
Iris Mj Kant
(IM)
Thecla Graas
(T)
Belle Toussaint
(B)
Sterre de Jong
(S)
Shahan Darwesh
(S)
Sandjiv S Mahes
(SS)
Dora Kamminga
(D)
Matthijs Koelewijn
(M)
Gino Faber
(G)
Guus Beaumont
(G)
Marije D Engel
(MD)
R Cheyenne N Pierie
(RCN)
Suzanne R Janssen
(SR)
Gino Faber
(G)
Edith van Dijkman
(E)
Jarom Heijmans
(J)
Yara Y Witte
(YY)
Rogers A Nahui Palomino
(RA)
Said Z Omar
(SZ)
Sonja Zweegman
(S)
Arnon P Kater
(AP)
Caya van den Vegt
(C)
Ilonka Arends-Halbesma
(I)
Emma de Pater
(E)
Margriet J Dijkstra
(MJ)
Nynke Y Rots
(NY)
Esther Siteur-van Rijnstra
(ES)
Dennis M de Rooij
(DM)
Rogier W Sanders
(RW)
Meliawati Poniman
(M)
Wouter Olijhoek
(W)
Jacqueline van Rijswijk
(J)
Tim Beaumont
(T)
Lusia Çetinel
(L)
Louis Schellekens
(L)
Yvonne M den Hartogh
(YM)
Jacqueline Cloos
(J)
Suzanne S Weijers
(SS)
Saïda Tonouh-Aajoud
(S)
Selime Avci
(S)
Elianne Roelandse-Koop
(E)
Willem A Dik
(WA)
Informations de copyright
© 2023 The Author(s).
Déclaration de conflit d'intérêts
T.M. received research grants from Celgene/BMS, Genentech, and Siemens, and received consulting fees from Kite/Gilead, Janssen, Lilly (all payments made to institution). All other authors declare no competing financial interests.
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