Evidence map›Paper›PMID 42553130›Full record

ArticleFrontiers in immunology2026

Spatial mapping of Ethiopian cutaneous leishmaniasis lesions reveals distinct tissue level immune programs.

Nidhi S Dey, Thao-Thy Pham, Shoumit Dey, Mekibib Kassa, Tigist Mekonnen, Helina Fikre, Pieter Monsieurs, Spatial Cl Consortium, Myrthe Pareyn, Johan van Griensven and 6 more

Abstract read
In one paragraph

Article in Frontiers in immunology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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

16 authors.

Nidhi S Dey *York Biomedical Research Institute, Hull York Medical School, University of York, York, United Kingdom.
Thao-Thy Pham *Department of Clinical Sciences, Institute of Tropical Medicine, Antwerp, Belgium.
Shoumit DeyYork Biomedical Research Institute, Hull York Medical School, University of York, York, United Kingdom.
Mekibib KassaLeishmaniasis Research and Treatment Centre, University of Gondar, Gondar, Ethiopia.
Tigist MekonnenLeishmaniasis Research and Treatment Centre, University of Gondar, Gondar, Ethiopia.
Helina FikreLeishmaniasis Research and Treatment Centre, University of Gondar, Gondar, Ethiopia.
Pieter MonsieursDepartment of Biomedical Sciences, Institute of Tropical Medicine, Antwerp, Belgium.
Spatial Cl ConsortiumYork Biomedical Research Institute, Hull York Medical School, University of York, York, United Kingdom.
Myrthe PareynDepartment of Clinical Sciences, Institute of Tropical Medicine, Antwerp, Belgium.
Johan van GriensvenDepartment of Clinical Sciences, Institute of Tropical Medicine, Antwerp, Belgium.
Malgorzata DomagalskaDepartment of Biomedical Sciences, Institute of Tropical Medicine, Antwerp, Belgium.
Jean-Claude DujardinDepartment of Biomedical Sciences, Institute of Tropical Medicine, Antwerp, Belgium.
Mezgebu Silamsaw AsresLeishmaniasis Research and Treatment Centre, University of Gondar, Gondar, Ethiopia.
Mikias WoldetensayDepartment of Dermatovenereology, University of Gondar, Gondar, Ethiopia.
Paul M KayeYork Biomedical Research Institute, Hull York Medical School, University of York, York, United Kingdom.
Wim AdriaensenDepartment of Clinical Sciences, Institute of Tropical Medicine, Antwerp, Belgium.

Funding

Wellcome Trust
6 · The paper itself

Abstract

Introduction: Human cutaneous leishmaniasis (CL) is a prevalent but neglected tropical disease characterised by inflammatory lesions that are either restricted to the site of the infected sand fly bite or disseminate to mucosae or within the skin. Compared to well-studied pre-clinical models, the nature and diversity of the tissue response in humans remains to be fully appreciated. Methods: We conducted an exploratory study using spatial transcriptomics on paired lesional and non-lesional skin punch biopsies from five Ethiopian CL patients (two infected with Results and Discussion: We identified spatially distinct immunopathological tissue responses including: i) epithelial hyperplasia with interferon-stimulated keratinocytes, ii) cytotoxicity with tertiary lymphoid structures, iii) granulomatous inflammation with proinflammatory response, iv) granulomatous inflammation with M2-polarised myeloid cell responses, and v) fibrotic remodelling with active collagen synthesis. Each patient in this case series exemplified one of these tissue responses, but immunopathological features were not mutually exclusive. This study extends our understanding of Ethiopian CL immunopathology and provides a molecular and cellular context that can be applied in larger clinical cohorts for testing hypotheses regarding the host and/or parasite determinants of CL disease diversity.

Indexed as

LeishmaniaLeishmaniasis, CutaneousSkinAdolescentAdultBiopsyEthiopiaFemaleHumansImmunohistochemistryKeratinocytesMaleMiddle AgedSpatial TranscriptomicsYoung Adultcutaneous leishmaniasisepithelial hyperplasiagranulomasimmunopathologyskinspatial transcriptomicstertiary lymphoid structures

Identifiers

PMID42553130
PMCPMC13433223

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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.