Evidence map›Paper›PMID 35143540›Full record

ArticlePloS one2022

Poor neutralization and rapid decay of antibodies to SARS-CoV-2 variants in vaccinated dialysis patients.

Jessica Bassi, Olivier Giannini, Chiara Silacci-Fregni, Laura Pertusini, Paolo Hitz, Tatiana Terrot, Yves Franzosi, Francesco Muoio, Christian Saliba, Marcel Meury and 25 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
3.3field-weighted citation impact, top 6% 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

16 citing papers in PubMed, 33 citations in OpenAlex.

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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

35 authors at 7 institutions in 4 countries.

Jessica BassiHumabs BioMed SA, A Subsidiary of Vir Biotechnology, Bellinzona, Switzerland.
Olivier GianniniFaculty of Biomedical Sciences, Università della Svizzera italiana, Lugano, Switzerland.
Chiara Silacci-FregniHumabs BioMed SA, A Subsidiary of Vir Biotechnology, Bellinzona, Switzerland.
Laura PertusiniDivision of Nephrology, Ente Ospedaliero Cantonale, Lugano, Switzerland.
Paolo HitzFaculty of Biomedical Sciences, Università della Svizzera italiana, Lugano, Switzerland.
Tatiana TerrotClinical Trial Unit, Ente Ospedaliero Cantonale, Lugano, Switzerland.
Yves FranzosiClinical Trial Unit, Ente Ospedaliero Cantonale, Lugano, Switzerland.
Francesco MuoioHumabs BioMed SA, A Subsidiary of Vir Biotechnology, Bellinzona, Switzerland.ORCID 0000-0003-4963-8665
Christian SalibaHumabs BioMed SA, A Subsidiary of Vir Biotechnology, Bellinzona, Switzerland.
Marcel MeuryVir Biotechnology, San Francisco, California, United States of America.
Exequiel A DellotaVir Biotechnology, San Francisco, California, United States of America.
Josh R DillenVir Biotechnology, San Francisco, California, United States of America.
Patrick HernandezVir Biotechnology, San Francisco, California, United States of America.
Nadine CzudnochowskiVir Biotechnology, San Francisco, California, United States of America.
Elisabetta CameroniHumabs BioMed SA, A Subsidiary of Vir Biotechnology, Bellinzona, Switzerland.
Nicola BeriaDivision of Nephrology, Ente Ospedaliero Cantonale, Lugano, Switzerland.
Mariangela VentrescaDivision of Nephrology, Ente Ospedaliero Cantonale, Lugano, Switzerland.
Alberto BadellinoDivision of Nephrology, Ente Ospedaliero Cantonale, Lugano, Switzerland.
Soraya Lavorato-HadjeresDivision of Nephrology, Ente Ospedaliero Cantonale, Lugano, Switzerland.
Elisabetta LecchiDivision of Nephrology, Ente Ospedaliero Cantonale, Lugano, Switzerland.
Tecla BonoraDivision of Nephrology, Ente Ospedaliero Cantonale, Lugano, Switzerland.
Matteo MattioloDivision of Nephrology, Ente Ospedaliero Cantonale, Lugano, Switzerland.
Guido TrinciDivision of Nephrology, Ente Ospedaliero Cantonale, Lugano, Switzerland.
Daniela GarzoniDivision of Nephrology, Ente Ospedaliero Cantonale, Lugano, Switzerland.
Giuseppe BonforteDivision of Nephrology, Ente Ospedaliero Cantonale, Lugano, Switzerland.
Valentina Forni-OgnaDivision of Nephrology, Ente Ospedaliero Cantonale, Lugano, Switzerland.
Davide GiunzioniDivision of Nephrology, Ente Ospedaliero Cantonale, Lugano, Switzerland.
Lorenzo BerwertDivision of Nephrology, Ente Ospedaliero Cantonale, Lugano, Switzerland.
Ravindra K GuptaCambridge Institute of Therapeutic Immunology & Infectious Disease (CITIID), Cambridge, United Kingdom.
Paolo FerrariFaculty of Biomedical Sciences, Università della Svizzera italiana, Lugano, Switzerland.ORCID 0000-0002-9619-3104
Alessandro CeschiFaculty of Biomedical Sciences, Università della Svizzera italiana, Lugano, Switzerland.
Pietro CippàDepartment of Medicine, Ente Ospedaliero Cantonale, Bellinzona, Switzerland.
Davide CortiHumabs BioMed SA, A Subsidiary of Vir Biotechnology, Bellinzona, Switzerland.
Antonio LanzavecchiaHumabs BioMed SA, A Subsidiary of Vir Biotechnology, Bellinzona, Switzerland.
Luca PiccoliHumabs BioMed SA, A Subsidiary of Vir Biotechnology, Bellinzona, Switzerland.ORCID 0000-0002-1085-6502
Ente Ospedaliero Cantonale · CHVir Biotechnology (Switzerland) · CHVIR Biotechnology (United States) · USUniversità della Svizzera italiana · CHUniversity of Cambridge · GBUniversity of Zurich · CHUNSW Sydney · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Patients on dialysis are at risk of severe course of SARS-CoV-2 infection. Understanding the neutralizing activity and coverage of SARS-CoV-2 variants of vaccine-elicited antibodies is required to guide prophylactic and therapeutic COVID-19 interventions in this frail population. By analyzing plasma samples from 130 hemodialysis and 13 peritoneal dialysis patients after two doses of BNT162b2 or mRNA-1273 vaccines, we found that 35% of the patients had low-level or undetectable IgG antibodies to SARS-CoV-2 Spike (S). Neutralizing antibodies against the vaccine-matched SARS-CoV-2 and Delta variant were low or undetectable in 49% and 77% of patients, respectively, and were further reduced against other emerging variants. The fraction of non-responding patients was higher in SARS-CoV-2-naïve hemodialysis patients immunized with BNT162b2 (66%) than those immunized with mRNA-1273 (23%). The reduced neutralizing activity correlated with low antibody avidity. Patients followed up to 7 months after vaccination showed a rapid decay of the antibody response with an average 21- and 10-fold reduction of neutralizing antibodies to vaccine-matched SARS-CoV-2 and Delta variant, which increased the fraction of non-responders to 84% and 90%, respectively. These data indicate that dialysis patients should be prioritized for additional vaccination boosts. Nevertheless, their antibody response to SARS-CoV-2 must be continuously monitored to adopt the best prophylactic and therapeutic strategy.

Indexed as

Neutralization TestsRenal DialysisVaccinationAnimalsAntibodies, NeutralizingAntibody AffinityCase-Control StudiesCHO CellsCOVID-19 VaccinesCricetulusDose-Response Relationship, ImmunologicFollow-Up StudiesHEK293 CellsHumansImmunoglobulin GmRNA VaccinesAntibodies, NeutralizingCOVID-19 VaccinesImmunoglobulin GmRNA Vaccines

Identifiers

PMID35143540
PMCPMC8830698
OpenAlexW4210992476

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.