Evidence map›Paper›PMID 34669144›Full record

ArticleJournal of clinical immunology2021

SARS-CoV-2 Vaccine Induced Atypical Immune Responses in Antibody Defects: Everybody Does their Best.

Ane Fernandez Salinas, Eva Piano Mortari, Sara Terreri, Concetta Quintarelli, Federica Pulvirenti, Stefano Di Cecca, Marika Guercio, Cinzia Milito, Livia Bonanni, Stefania Auria and 9 more

Open access · hybridAbstract read
In one paragraph

Article in Journal of clinical immunology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 63 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
63citing papers in PubMed, 1 pooled it
5.1field-weighted citation impact, top 4% 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

63 citing papers in PubMed, 1 synthesis or guideline pooled it, 85 citations in OpenAlex.

  1. Pooled it
  2. Elevated CD21Journal of clinical immunology · 2022
    Trial
  3. Observational
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  5. Article
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  7. Review
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  10. Article
  11. Observational
  12. Article
  13. Review
  14. T Cell Abnormalities in X-Linked Agammaglobulinaemia: an Updated Review.Clinical reviews in allergy & immunology · 2023
    Review
  15. Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. Article

3 more citing papers are in PubMed but not listed here.

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

19 authors at 4 institutions in 1 country.

Ane Fernandez SalinasDepartment of Molecular Medicine, Sapienza University of Rome, Viale Dell'Università, 37, Rome, Italy.
Eva Piano MortariDiagnostic Immunology Research Unit, Multimodal Medicine Research Area, Bambino Gesù Children's Hospital, IRCCS, Viale Di San Paolo, 15, Rome, Italy.
Sara TerreriDiagnostic Immunology Research Unit, Multimodal Medicine Research Area, Bambino Gesù Children's Hospital, IRCCS, Viale Di San Paolo, 15, Rome, Italy.
Concetta QuintarelliDepartment Onco-Haematology, and Cell and Gene Therapy, Bambino Gesù Children Hospital, IRCCS, Rome, Italy.
Federica PulvirentiRegional Reference Centre for Primary Immune Deficiencies, Azienda Ospedaliera Universitaria Policlinico Umberto I, Rome, Italy.
Stefano Di CeccaDepartment Onco-Haematology, and Cell and Gene Therapy, Bambino Gesù Children Hospital, IRCCS, Rome, Italy.
Marika GuercioDepartment Onco-Haematology, and Cell and Gene Therapy, Bambino Gesù Children Hospital, IRCCS, Rome, Italy.
Cinzia MilitoDepartment of Molecular Medicine, Sapienza University of Rome, Viale Dell'Università, 37, Rome, Italy.
Livia BonanniRegional Reference Centre for Primary Immune Deficiencies, Azienda Ospedaliera Universitaria Policlinico Umberto I, Rome, Italy.
Stefania AuriaDepartment of Molecular Medicine, Sapienza University of Rome, Viale Dell'Università, 37, Rome, Italy.
Laura RomaggioliDepartment of Molecular Medicine, Sapienza University of Rome, Viale Dell'Università, 37, Rome, Italy.
Giuseppina CusanoDepartment of Molecular Medicine, Sapienza University of Rome, Viale Dell'Università, 37, Rome, Italy.
Christian AlbanoDiagnostic Immunology Research Unit, Multimodal Medicine Research Area, Bambino Gesù Children's Hospital, IRCCS, Viale Di San Paolo, 15, Rome, Italy.
Salvatore ZaffinaOccupational Medicine/Health Technology Assessment and Safety Research Unit, Clinical-Technological Innovations Research Area, Bambino Gesù Children's Hospital, IRCCS, Viale di San Paolo, 15, Rome, Italy.
Carlo Federico PernoMultimodal Medicine Research Area, Bambino Gesù Children's Hospital, IRCCS, Piazza Sant'Onofrio, 4, Rome, Italy.
Giuseppe SpadaroDepartment of Translational Medical Sciences, University of Naples Federico II, 80131, Naples, Italy.
Franco LocatelliDepartment Onco-Haematology, and Cell and Gene Therapy, Bambino Gesù Children Hospital, IRCCS, Rome, Italy.
Rita Carsetti *Diagnostic Immunology Research Unit, Multimodal Medicine Research Area, Bambino Gesù Children's Hospital, IRCCS, Viale Di San Paolo, 15, Rome, Italy.
Isabella Quinti *Department of Molecular Medicine, Sapienza University of Rome, Viale Dell'Università, 37, Rome, Italy. isabella.quinti@uniroma1.it.ORCID http://orcid.org/0000-0002-3328-7584
Bambino Gesù Children's Hospital · ITSapienza University of Rome · ITPoliclinico Umberto I · ITUniversity of Naples Federico II · IT

Funding

ministero della salute COVID-2020-12371817ministero della salute RF2013-02358960
6 · The paper itself

Abstract

backgroundData on immune responses to SARS-CoV-2 in patients with Primary Antibody Deficiencies (PAD) are limited to infected patients and to heterogeneous cohorts after immunization.

methodsForty-one patients with Common Variable Immune Deficiencies (CVID), six patients with X-linked Agammaglobulinemia (XLA), and 28 healthy age-matched controls (HD) were analyzed for anti-Spike and anti-receptor binding domain (RBD) antibody production, generation of Spike-specific memory B-cells, and Spike-specific T-cells before vaccination and one week after the second dose of BNT162b2 vaccine.

resultsThe vaccine induced Spike-specific IgG and IgA antibody responses in all HD and in 20% of SARS-CoV-2 naive CVID patients. Anti-Spike IgG were detectable before vaccination in 4 out 7 CVID previously infected with SARS-CoV-2 and were boosted in six out of seven patients by the subsequent immunization raising higher levels than patients naïve to infection. While HD generated Spike-specific memory B-cells, and RBD-specific B-cells, CVID generated Spike-specific atypical B-cells, while RBD-specific B-cells were undetectable in all patients, indicating the incapability to generate this new specificity. Specific T-cell responses were evident in all HD and defective in 30% of CVID. All but one patient with XLA responded by specific T-cell only.

conclusionIn PAD patients, early atypical immune responses after BNT162b2 immunization occurred, possibly by extra-follicular or incomplete germinal center reactions. If these responses to vaccination might result in a partial protection from infection or reinfection is now unknown. Our data suggests that SARS-CoV-2 infection more effectively primes the immune response than the immunization alone, possibly suggesting the need for a third vaccine dose for patients not previously infected.

Indexed as

Antibodies, ViralCOVID-19COVID-19 VaccinesHumansImmunoglobulin GImmunologic Deficiency SyndromesImmunologic MemoryLymphocytesSARS-CoV-2Spike Glycoprotein, CoronavirusAntibodies, ViralCOVID-19 VaccinesImmunoglobulin GSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2BNT162b2 vaccineCommon variable immune deficienciesCOVID-19Memory cellsPrimary antibody deficienciesReceptor-binding-domainSARS-CoV-2Spike proteinX-linked agammaglobulinemia

Identifiers

PMID34669144
PMCPMC8527979
OpenAlexW3206020366

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.