Evidence map›Paper›PMID 39653555›Full record

ArticleJournal for immunotherapy of cancer2024

DNA barcoded peptide-MHC multimers to measure and monitor minor histocompatibility antigen-specific T cells after allogeneic stem cell transplantation.

Kyra J Fuchs, Marcus Göransson, Michel G D Kester, Natasja W Ettienne, Marian van de Meent, Rob C M de Jong, Eva A S Koster, Constantijn J M Halkes, Ferenc Scheeren, Mirjam H M Heemskerk and 4 more

Abstract read
In one paragraph

Article in Journal for immunotherapy of cancer, 2024. 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. Review
  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

14 authors.

Kyra J Fuchs *Department of Hematology, Leiden University Medical Center, Leiden, The Netherlands.ORCID 0000-0002-4704-8218
Marcus Göransson *Department of Health Technology, Technical University of Denmark, Lyngby, Denmark.
Michel G D KesterDepartment of Hematology, Leiden University Medical Center, Leiden, The Netherlands.
Natasja W EttienneDepartment of Health Technology, Technical University of Denmark, Lyngby, Denmark.
Marian van de MeentDepartment of Hematology, Leiden University Medical Center, Leiden, The Netherlands.
Rob C M de JongDepartment of Hematology, Leiden University Medical Center, Leiden, The Netherlands.
Eva A S KosterDepartment of Hematology, Leiden University Medical Center, Leiden, The Netherlands.ORCID 0000-0002-8446-5133
Constantijn J M HalkesDepartment of Hematology, Leiden University Medical Center, Leiden, The Netherlands.
Ferenc ScheerenDepartment of Dermatology, Leiden University Medical Center, Leiden, The Netherlands.ORCID 0000-0002-8304-9023
Mirjam H M HeemskerkDepartment of Hematology, Leiden University Medical Center, Leiden, The Netherlands.ORCID 0000-0001-6320-9133
Peter van BalenDepartment of Hematology, Leiden University Medical Center, Leiden, The Netherlands.
J H Frederik FalkenburgDepartment of Hematology, Leiden University Medical Center, Leiden, The Netherlands.
Sine R HadrupDepartment of Health Technology, Technical University of Denmark, Lyngby, Denmark.ORCID 0000-0002-5937-4344
Marieke GriffioenDepartment of Hematology, Leiden University Medical Center, Leiden, The Netherlands m.griffioen@lumc.nl.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Allogeneic stem cell transplantation (alloSCT) provides a curative treatment option for hematological malignancies. After HLA-matched alloSCT, donor-derived T cells recognize minor histocompatibility antigens (MiHAs), which are polymorphic peptides presented by HLA on patient cells. MiHAs are absent on donor cells due to genetic differences between patient and donor. T cells targeting broadly expressed MiHAs induce graft-versus-leukemia (GvL) reactivity as well as graft-versus-host disease (GvHD), while T cells for MiHAs with restricted or preferential expression on hematopoietic or non-hematopoietic cells may skew responses toward GvL or GvHD, respectively. Besides tissue expression, overall strength of GvL and GvHD is also determined by T-cell frequencies against MiHAs.Here, we explored the use of DNA barcode-labeled peptide-MHC multimers to detect and monitor antigen-specific T cells for the recently expanded repertoire of HLA-I-restricted MiHAs. In 16 patients who experienced an immune response after donor lymphocyte infusion, variable T-cell frequencies up to 30.5% of CD8

Indexed as

Graft vs Host DiseaseMinor Histocompatibility AntigensTransplantation, HomologousAdultAgedCD8-Positive T-LymphocytesFemaleGraft vs Leukemia EffectHematopoietic Stem Cell TransplantationHumansMaleMiddle AgedPeptidesStem Cell TransplantationMinor Histocompatibility AntigensPeptidesGraft versus host disease - GVHDGraft versus leukemiaHematologic MalignanciesT cellTransplant

Identifiers

PMID39653555
PMCPMC11629015

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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.