Evidence map›Paper›PMID 41540511›Full record

ReviewInfectious diseases of poverty2026

From dogma to data: charting a path forward for clinico-immunological research in Ethiopian cutaneous leishmaniasis.

Thao-Thy Pham, Saskia van Henten, Mikias Woldetensay, Mezgebu Silamsaw Asres, Eleni Ayele, Paul M Kaye, Malgorzata Anna Domagalska, Jean-Claude Dujardin, Johan van Griensven, Wim Adriaensen and 1 more

Abstract readReview
In one paragraph

Review in Infectious diseases of poverty, 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. 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

11 authors.

Thao-Thy PhamDepartment of Clinical Sciences, Institute of Tropical Medicine Antwerp, Antwerp, Belgium. thaothypham@itg.be.
Saskia van HentenDepartment of Clinical Sciences, Institute of Tropical Medicine Antwerp, Antwerp, Belgium.
Mikias WoldetensayDepartment of Dermatology and Venereology, University of Gondar, Gondar, Ethiopia.
Mezgebu Silamsaw AsresDepartment of Internal Medicine, University of Gondar, Gondar, Ethiopia.
Eleni AyeleDepartment of Internal Medicine, University of Gondar, Gondar, Ethiopia.
Paul M KayeYork Biomedical Research Institute and Hull York Medical School, University of York, York, UK.
Malgorzata Anna DomagalskaDepartment of Biomedical Sciences, Institute of Tropical Medicine Antwerp, Antwerp, Belgium.
Jean-Claude DujardinDepartment of Biomedical Sciences, Institute of Tropical Medicine Antwerp, Antwerp, Belgium.
Johan van GriensvenDepartment of Clinical Sciences, Institute of Tropical Medicine Antwerp, Antwerp, Belgium.
Wim AdriaensenDepartment of Clinical Sciences, Institute of Tropical Medicine Antwerp, Antwerp, Belgium.
Spatial CL Consortium

Funding

Stichting Dioraphte 20200033
6 · The paper itself

Abstract

backgroundRooted in long-standing assumptions and adapted from classifications mainly used for Latin American cutaneous leishmaniasis (CL), the nationally recommended clinical categories in Ethiopia for CL remain limited to localized cutaneous leishmaniasis (LCL), mucocutaneous leishmaniasis (MCL), and diffuse cutaneous leishmaniasis (DCL). However, these categories are associated with immune mechanisms which have not been validated in the Ethiopian context and thus risk misrepresenting the true clinical and immunopathological diversity. In this opinion piece, we will therefore outline key knowledge gaps and challenges in current clinico-immunological research on Ethiopian CL. MAIN BODY: In Ethiopia, Leishmania aethiopica is often assumed as the causative agent of these 'LCL', 'MCL' and 'DCL' forms, yet significant gaps in knowledge urge caution. For example, adoption of this 'LCL', 'MCL' and 'DCL' terminology and the associated immune mechanisms has led to inconsistent results. Most immunological studies on Ethiopian CL have focused on peripheral blood, resulting in little information about immune processes in the lesion, the original site of infection. Adding to the complexity, other species (including L. major, L. donovani and L. tropica as well as L. aethiopica hybrids) also circulate, with reports of Leishmania RNA virus co-infection. To address these challenges, we propose a multidimensional approach that combines standardized clinical documentation with appropriate lesion and blood sampling for in-depth profiling of both immune responses and parasite diversity. Adopting this holistic approach will require inclusive (inter)national collaborations with a focus on promoting equitable biobank and data sharing which will strengthen local research capacities.

conclusionsBy addressing the main challenges and knowledge gaps in current clinico-immunological research through a multidimensional approach, this opinion aims to provide the tools to achieve a better and unbiased understanding of the immunopathogenesis of Ethiopian CL, a severe yet under-investigated disease. Such progress is essential for improving CL management in Ethiopia and aligns with the World Health Organization priority on controlling CL.

Indexed as

LeishmaniaLeishmaniasis, CutaneousEthiopiaHumansClinico-immunologyCutaneous leishmaniasisEthiopiaImmunoparasitologyImmunopathogenesisLeishmania aethiopicaLeishmaniasis

Identifiers

PMID41540511
PMCPMC12810004

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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.