Evidence map›Paper›PMID 36854892›Full record

ArticleBone marrow transplantation2023

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.

José Luis Piñana, Rodrigo Martino, Lourdes Vazquez, Lucia López-Corral, Ariadna Pérez, Pedro Chorão, Alejandro Avendaño-Pita, María-Jesús Pascual, Andrés Sánchez-Salinas, Gabriela Sanz-Linares and 19 more

Open access · bronzeAbstract readMulticenter Study
In one paragraph

Article in Bone marrow transplantation, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 3 pooled it
6.6field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

18 citing papers in PubMed, 3 syntheses or guidelines pooled it, 32 citations in OpenAlex.

  1. Pooled it
  2. Vaccination of Adults With Cancer: ASCO Guideline.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2024
    Guideline
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

29 authors at 13 institutions in 1 country.

José Luis PiñanaHematology Department, Hospital Clínico Universitario de Valencia, Valencia, Spain. jlpinana@gmail.com.ORCID 0000-0001-8533-2562
Rodrigo MartinoHematology Division, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain.ORCID 0000-0001-5143-4042
Lourdes VazquezHematology Department, University Hospital of Salamanca (HUS/IBSAL), CIBERONC and Cancer Research Institute of Salamanca-IBMCC (USAL-CSIC), 37007, Salamanca, Spain.ORCID 0000-0001-8191-0046
Lucia López-CorralHematology Department, University Hospital of Salamanca (HUS/IBSAL), CIBERONC and Cancer Research Institute of Salamanca-IBMCC (USAL-CSIC), 37007, Salamanca, Spain.
Ariadna PérezHematology Department, Hospital Clínico Universitario de Valencia, Valencia, Spain.
Pedro ChorãoHematology Division, Hospital universitario y politécnico La Fe, Valencia, Spain.ORCID 0000-0001-6741-971X
Alejandro Avendaño-PitaHematology Department, University Hospital of Salamanca (HUS/IBSAL), CIBERONC and Cancer Research Institute of Salamanca-IBMCC (USAL-CSIC), 37007, Salamanca, Spain.
María-Jesús PascualHematology Division, Hospital Regional Universitario Carlos Haya, Malaga, Spain.
Andrés Sánchez-SalinasHematology Division, Hospital Clínico Universitario Virgen de la Arrixaca, Murcia, Spain.
Gabriela Sanz-LinaresHematology Division, Institut Català Oncologia-Hospital Duran i reynals, Barcelona, Spain.
María T OlaveHematology Division, Hospital Clínico Universitario Lozano Blesa, IIS Aragon, Zaragoza, Spain.
Ignacio ArroyoHematology Department, Hospital Clínico Universitario de Valencia, Valencia, Spain.
Mar TormoFundación INCLIVA, Instituto de Investigación Sanitaria Hospital Clínico Universitario de Valencia, Valencia, Spain.ORCID 0000-0001-9622-1649
Lucia VillalonHematology Division, Hospital Universitario Fundación Alcorcón, Madrid, Spain.
Venancio Conesa-GarciaHematology Division, Hospital General universitari d'Elx, Elche, Spain.ORCID 0000-0002-6412-3419
Beatriz GagoHematology Division, Hospital Regional Universitario Carlos Haya, Malaga, Spain.
María-José TerolHematology Department, Hospital Clínico Universitario de Valencia, Valencia, Spain.
Marta VillalbaHematology Division, Hospital universitario y politécnico La Fe, Valencia, Spain.
Valentín Garcia-GutierrezHematology Division, Hospital Ramon y Cajal, IRYCIS, Madrid, Spain.ORCID 0000-0003-4752-0815
Almudena CaberoHematology Department, University Hospital of Salamanca (HUS/IBSAL), CIBERONC and Cancer Research Institute of Salamanca-IBMCC (USAL-CSIC), 37007, Salamanca, Spain.
José Ángel Hernández-RivasHematology Division, Hospital Universitario Infanta Leonor. Department of Medicine. Complutense University, Madrid, Spain.
Elena FerrerHematology Department, Hospital Clínico Universitario de Valencia, Valencia, Spain.
Irene García-CadenasHematology Division, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain.ORCID 0000-0002-2994-9055
Anabel TeruelHematology Department, Hospital Clínico Universitario de Valencia, Valencia, Spain.ORCID 0000-0003-1559-7607
David NavarroFundación INCLIVA, Instituto de Investigación Sanitaria Hospital Clínico Universitario de Valencia, Valencia, Spain.ORCID 0000-0003-3010-4110
Ángel CedilloHematopoietic Stem Cell Transplantation and Cell Therapy Group (GETH), Valencia, Spain.
Anna SuredaHematology Division, Institut Català Oncologia-Hospital Duran i reynals, Barcelona, Spain.
Carlos SolanoHematology Department, Hospital Clínico Universitario de Valencia, Valencia, Spain.ORCID 0000-0003-3702-0817
Spanish Hematopoietic Stem Cell Transplantation and Cell Therapy Group (GETH-TC)
Hospital Clínico Universitario de Valencia · ESInstituto de Investigación Biomédica de Salamanca · ESDuran i Reynals Hospital · ESHospital de Sant Pau · ESHospital Regional Universitario de Málaga · ESHospital Universitari i Politècnic La Fe · ESHospital Clínico Universitario Lozano Blesa · ESHospital General Universitario de Elche · ESHospital Universitario Fundación Alcorcón · ESHospital Universitario Infanta Leonor · ESHospital Universitario Virgen de la Arrixaca · ESInstituto Ramón y Cajal de Investigación Sanitaria · ESUniversitat de València · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

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.

Indexed as

COVID-19Hematopoietic Stem Cell TransplantationReceptors, Chimeric AntigenAntibodies, ViralBreakthrough InfectionsCell- and Tissue-Based TherapyCohort StudiesHumansProspective StudiesSARS-CoV-2Transplantation, AutologousTransplant RecipientsVaccinationAntibodies, ViralReceptors, Chimeric Antigen

Identifiers

PMID36854892
PMCPMC9974060
OpenAlexW4322603814

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.