SARS-CoV-2-reactive antibody waning, booster effect and breakthrough SARS-CoV-2 infection in hematopoietic stem cell transplant and cell therapy recipients at one year after vaccination.


Journal

Bone marrow transplantation
ISSN: 1476-5365
Titre abrégé: Bone Marrow Transplant
Pays: England
ID NLM: 8702459

Informations de publication

Date de publication:
05 2023
Historique:
received: 08 11 2022
accepted: 20 02 2023
revised: 13 02 2023
medline: 8 5 2023
pubmed: 2 3 2023
entrez: 1 3 2023
Statut: ppublish

Résumé

The kinetics of SARS-CoV-2 reactive IgG antibodies after full vaccination and booster in allogeneic and autologous stem cell transplantation (allo-HSCT, ASCT) and chimeric antigen receptor T-cell therapy (CAR-T) are of utmost importance for estimating risk of infection. A prospective multicenter registry-based cohort study, conducted from December 2020 to July 2022 was used to analyze antibody waning over time, booster effect and the relationship of antibody response and breakthrough infection in 572 recipients (429 allo-HSCT, 121 ASCT and 22 CAR-T cell therapy). A significant decline in antibody titers was observed at 3 and 6 months after full vaccination in recipients without pre-vaccine SARS-CoV-2 infection, whereas recipients infected prior to vaccination showed higher and stable antibody titers over time. In poor responders, a booster dose was able to increase antibody titers in 83% of allo-HSCT and 58% of ASCT recipients but not in CART-T cell recipients [0%] (p < 0.01). One-year cumulative incidence of breakthrough infection was 15%, similar among cell therapy procedures. Immunosuppressive drugs at the time of vaccination [hazard ratio (HR) 1.81, p = 0.0028] and reduced intensity conditioning (HR 0.49, p = 0.011) were identified as the only conditions associated with different risk of breakthrough infection in allo-HSCT recipients. Antibody titers were associated with breakthrough infection and disease severity. No death was observed among the 72 breakthrough infections. Antibody level decay after the first two vaccine doses was common except in recipients with pre-vaccination SARS-CoV-2 infection. Poorly responding allo-HSCT recipients showed a response advantage with the booster as compared to ASCT and, especially, the null response found in CAR-T cell recipients. Antibody titers were positively correlated with the risk of breakthrough SARS-CoV-2 infection which was mainly driven by the immunosuppression status.

Identifiants

pubmed: 36854892
doi: 10.1038/s41409-023-01946-0
pii: 10.1038/s41409-023-01946-0
pmc: PMC9974060
doi:

Substances chimiques

Receptors, Chimeric Antigen 0
Antibodies, Viral 0

Types de publication

Multicenter Study Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

567-580

Informations de copyright

© 2023. The Author(s), under exclusive licence to Springer Nature Limited.

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Auteurs

José Luis Piñana (JL)

Hematology Department, Hospital Clínico Universitario de Valencia, Valencia, Spain. jlpinana@gmail.com.
Fundación INCLIVA, Instituto de Investigación Sanitaria Hospital Clínico Universitario de Valencia, Valencia, Spain. jlpinana@gmail.com.

Rodrigo Martino (R)

Hematology Division, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain.

Lourdes Vazquez (L)

Hematology Department, University Hospital of Salamanca (HUS/IBSAL), CIBERONC and Cancer Research Institute of Salamanca-IBMCC (USAL-CSIC), 37007, Salamanca, Spain.

Lucia López-Corral (L)

Hematology Department, University Hospital of Salamanca (HUS/IBSAL), CIBERONC and Cancer Research Institute of Salamanca-IBMCC (USAL-CSIC), 37007, Salamanca, Spain.

Ariadna Pérez (A)

Hematology Department, Hospital Clínico Universitario de Valencia, Valencia, Spain.
Fundación INCLIVA, Instituto de Investigación Sanitaria Hospital Clínico Universitario de Valencia, Valencia, Spain.

Pedro Chorão (P)

Hematology Division, Hospital universitario y politécnico La Fe, Valencia, Spain.

Alejandro Avendaño-Pita (A)

Hematology Department, University Hospital of Salamanca (HUS/IBSAL), CIBERONC and Cancer Research Institute of Salamanca-IBMCC (USAL-CSIC), 37007, Salamanca, Spain.

María-Jesús Pascual (MJ)

Hematology Division, Hospital Regional Universitario Carlos Haya, Malaga, Spain.

Andrés Sánchez-Salinas (A)

Hematology Division, Hospital Clínico Universitario Virgen de la Arrixaca, Murcia, Spain.

Gabriela Sanz-Linares (G)

Hematology Division, Institut Català Oncologia-Hospital Duran i reynals, Barcelona, Spain.

María T Olave (MT)

Hematology Division, Hospital Clínico Universitario Lozano Blesa, IIS Aragon, Zaragoza, Spain.

Ignacio Arroyo (I)

Hematology Department, Hospital Clínico Universitario de Valencia, Valencia, Spain.

Mar Tormo (M)

Fundación INCLIVA, Instituto de Investigación Sanitaria Hospital Clínico Universitario de Valencia, Valencia, Spain.

Lucia Villalon (L)

Hematology Division, Hospital Universitario Fundación Alcorcón, Madrid, Spain.

Venancio Conesa-Garcia (V)

Hematology Division, Hospital General universitari d'Elx, Elche, Spain.

Beatriz Gago (B)

Hematology Division, Hospital Regional Universitario Carlos Haya, Malaga, Spain.

María-José Terol (MJ)

Hematology Department, Hospital Clínico Universitario de Valencia, Valencia, Spain.
Fundación INCLIVA, Instituto de Investigación Sanitaria Hospital Clínico Universitario de Valencia, Valencia, Spain.

Marta Villalba (M)

Hematology Division, Hospital universitario y politécnico La Fe, Valencia, Spain.

Valentín Garcia-Gutierrez (V)

Hematology Division, Hospital Ramon y Cajal, IRYCIS, Madrid, Spain.

Almudena Cabero (A)

Hematology Department, University Hospital of Salamanca (HUS/IBSAL), CIBERONC and Cancer Research Institute of Salamanca-IBMCC (USAL-CSIC), 37007, Salamanca, Spain.

José Ángel Hernández-Rivas (JÁ)

Hematology Division, Hospital Universitario Infanta Leonor. Department of Medicine. Complutense University, Madrid, Spain.

Elena Ferrer (E)

Hematology Department, Hospital Clínico Universitario de Valencia, Valencia, Spain.
Fundación INCLIVA, Instituto de Investigación Sanitaria Hospital Clínico Universitario de Valencia, Valencia, Spain.

Irene García-Cadenas (I)

Hematology Division, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain.

Anabel Teruel (A)

Hematology Department, Hospital Clínico Universitario de Valencia, Valencia, Spain.
Fundación INCLIVA, Instituto de Investigación Sanitaria Hospital Clínico Universitario de Valencia, Valencia, Spain.

David Navarro (D)

Fundación INCLIVA, Instituto de Investigación Sanitaria Hospital Clínico Universitario de Valencia, Valencia, Spain.
Microbiology department, Hospital Clinico Universitario de Valencia, Valencia, Spain.

Ángel Cedillo (Á)

Hematopoietic Stem Cell Transplantation and Cell Therapy Group (GETH), Valencia, Spain.

Anna Sureda (A)

Hematology Division, Institut Català Oncologia-Hospital Duran i reynals, Barcelona, Spain.

Carlos Solano (C)

Hematology Department, Hospital Clínico Universitario de Valencia, Valencia, Spain.
Fundación INCLIVA, Instituto de Investigación Sanitaria Hospital Clínico Universitario de Valencia, Valencia, Spain.
Department of Medicine, School of Medicine. University of Valencia, Valencia, Spain.

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Classifications MeSH