Evidence map›Paper›PMID 40898724›Full record

ArticleBrain and behavior2025

De Novo Immune Induction After COVID-19 Vaccination Under B-Cell Depletion Is Characterized by Robust T-Cellular Immunity in Patients With Inflammatory Central Nervous System Disease.

Mathias Fousse, Verena Klemis, Saskia Bronder, Rebecca Urschel, Franziska Hielscher, Klaus Faßbender, Urban Sester, Martina Sester, Tina Schmidt

Abstract read
In one paragraph

Article in Brain and behavior, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Article
  2. Article
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

9 authors.

Mathias FousseDepartment of Neurology, Saarland University, Homburg, Germany.ORCID https://orcid.org/0000-0001-5489-1492
Verena KlemisDepartment of Transplant and Infection Immunology, Saarland University, Homburg, Germany.ORCID https://orcid.org/0000-0002-5636-1273
Saskia BronderDepartment of Transplant and Infection Immunology, Saarland University, Homburg, Germany.ORCID https://orcid.org/0000-0001-5863-1268
Rebecca UrschelDepartment of Transplant and Infection Immunology, Saarland University, Homburg, Germany.ORCID https://orcid.org/0009-0008-2677-5118
Franziska HielscherDepartment of Transplant and Infection Immunology, Saarland University, Homburg, Germany.ORCID https://orcid.org/0000-0001-8527-8412
Klaus FaßbenderDepartment of Neurology, Saarland University, Homburg, Germany.ORCID https://orcid.org/0000-0003-3596-868X
Urban SesterSHG Kliniken, Völklingen, Germany.ORCID https://orcid.org/0000-0003-4007-5595
Martina SesterDepartment of Transplant and Infection Immunology, Saarland University, Homburg, Germany.ORCID https://orcid.org/0000-0001-5482-0002
Tina SchmidtDepartment of Transplant and Infection Immunology, Saarland University, Homburg, Germany.ORCID https://orcid.org/0000-0001-7929-5283

Funding

German Federal ministry of Education and Research COVIM 2.0German Federal ministry of Education and Research FZK 01KX2121State Chancellery of the Saarland
6 · The paper itself

Abstract

backgroundImmune induction under B-cell depletion is complex and far from being fully understood.

methodsWe investigated clinical and immunological responses after dual homologous mRNA vaccination with BNT162b2 and after booster vaccination or infection in 14 B-cell depleted patients with inflammatory central nervous system disease in comparison to 28 healthy controls. Spike-specific IgG were determined using ELISA and neutralizing activity by surrogate assay. Reactive T cells were flow-cytometrically analyzed after spike-specific and polyclonal stimulation. Reactogenicity was self-reported using a questionnaire.

resultsVaccination was well tolerated, with slightly more systemic events reported by patients. Spike-specific antibodies were induced in all controls, but only 43% of patients with significantly lower IgG levels and reduced neutralizing capacity (p < 0.0001). In contrast, spike-reactive T cells were induced in both groups with similar CD4 and higher CD8 T-cell levels in patients. Functional characterization of spike-reactive T cells revealed equally high CTLA-4 expression in both groups, but higher proportions of polyfunctional, triple-cytokine expressing CD4 and CD8 T cells in patients especially after the third immunization. Three patients experienced mild breakthrough infections after second vaccination.

conclusionsDespite limited ability of B-cell depleted patients to mount a humoral immune response after multiple doses of SARS-CoV-2 mRNA vaccination, the vaccine-induced T-cell response is robust, which may have implications for protection against severe disease.

Indexed as

B-LymphocytesCOVID-19COVID-19 VaccinesImmunity, CellularT-LymphocytesAdultAgedAntibodies, NeutralizingAntibodies, ViralBNT162 VaccineCD8-Positive T-LymphocytesFemaleHumansImmunoglobulin GLymphocyte DepletionMaleAntibodies, NeutralizingAntibodies, ViralBNT162 VaccineCOVID-19 VaccinesImmunoglobulin GSpike Glycoprotein, CoronavirusB‐cell depletionmultiple sclerosisSARS‐CoV‐2T cellsvaccination

Identifiers

PMID40898724
PMCPMC12405670

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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.