Evidence map›Paper›PMID 40145092›Full record

ArticleFrontiers in immunology2025

The XBB.1.5 mRNA booster vaccine does not significantly increase the percentage of XBB.1.5 mono-reactive T cells.

Joel Sop, Alicia Mercado, Alexis Figueroa, Tyler P Beckey, Caroline C Traut, Li Zhang, Kellie N Smith, Joel N Blankson

Abstract read
In one paragraph

Article in Frontiers in immunology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. 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

8 authors.

Joel SopDepartment of Medicine, Johns Hopkins Medicine, Baltimore, MD, United States.
Alicia MercadoDepartment of Medicine, Johns Hopkins Medicine, Baltimore, MD, United States.
Alexis FigueroaDepartment of Medicine, Johns Hopkins Medicine, Baltimore, MD, United States.
Tyler P BeckeyDepartment of Medicine, Johns Hopkins Medicine, Baltimore, MD, United States.
Caroline C TrautDepartment of Medicine, Johns Hopkins Medicine, Baltimore, MD, United States.
Li ZhangBloomberg-Kimmel Institute for Cancer Immunotherapy, Johns Hopkins Medicine, Baltimore, MD, United States.
Kellie N Smith *Bloomberg-Kimmel Institute for Cancer Immunotherapy, Johns Hopkins Medicine, Baltimore, MD, United States.
Joel N Blankson *Department of Medicine, Johns Hopkins Medicine, Baltimore, MD, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recent efforts in vaccine development have targeted spike proteins from evolving SARS-CoV-2 variants. In this study, we analyzed T cell responses to the XBB.1.5 and BA.2.86 subvariants in individuals who previously received bivalent vaccines containing mRNA for ancestral and BA.5 spike proteins. T cell-mediated cytokine responses to spike proteins from both variants were largely preserved. To determine the mechanism of this preserved recognition, we utilized the functional expansion of specific T cells (FEST) assay to distinguish between the presence of T cells that cross-recognized ancestral and variant epitopes versus distinct populations of T cells that were mono-reactive for ancestral or variant epitopes. We found the majority of spike-specific T cells cross-recognized the ancestral spike and the XBB.1.5 and BA.2.86 subvariants, with less than 10% of T cells being mono-reactive for either variant. Interestingly, immunization with the XBB.1.5 monovalent booster vaccine did not significantly increase the percentage of XBB.1.5 mono-reactive T cells. Our results suggest a potential limitation in the induction of mono-reactive T cell responses by variant-specific booster vaccines.

Indexed as

COVID-19COVID-19 VaccinesSARS-CoV-2Spike Glycoprotein, CoronavirusT-LymphocytesAdultCross ReactionsEpitopes, T-LymphocyteFemaleHumansImmunization, SecondaryMaleMiddle AgedmRNA VaccinesCOVID-19 VaccinesEpitopes, T-LymphocytemRNA VaccinesSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2BA.2.86bivalent vaccineSARS-CoV-2T cell receptorXBB.1.5

Identifiers

PMID40145092
PMCPMC11936820

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.