Evidence map›Paper›PMID 41758879›Full record

ArticlePLoS neglected tropical diseases2026

Systemic inflammatory markers of visceral leishmaniasis treatment response in East Africa.

Ayenew Addisu, Alice Bayiyana, João L Reis Cunha, Daniel Matano, Brima M Younis, Karen Hogg, Rebecca Wiggins, Wilson Biwott, Finnley Osuna, Christine Ichugu and 18 more

Abstract readMulticenter Study
In one paragraph

Article in PLoS neglected tropical diseases, 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

28 authors.

Ayenew AddisuDepartment of Medical Parasitology, School of Biomedical and Laboratory Sciences, College of Medicine and Health Sciences, University of Gondar, Gondar, Ethiopia.
Alice BayiyanaDepartment of Immunology and Molecular Biology, Makerere University, Kampala, Uganda.
João L Reis CunhaYork Biomedical Research Institute, Hull York Medical School, University of York, York, United Kingdom.
Daniel MatanoCenter for Clinical Research, Kenya Medical Research Institute, Nairobi, Kenya.
Brima M YounisInstitute of Endemic Diseases, Khartoum, Sudan.
Karen HoggBioSciences Technology Facility, Dept of Biology, University of York, York, United Kingdom.
Rebecca WigginsYork Biomedical Research Institute, Hull York Medical School, University of York, York, United Kingdom.
Wilson BiwottCenter for Clinical Research, Kenya Medical Research Institute, Nairobi, Kenya.
Finnley OsunaCenter for Clinical Research, Kenya Medical Research Institute, Nairobi, Kenya.
Christine IchuguCenter for Clinical Research, Kenya Medical Research Institute, Nairobi, Kenya.
Ayalew Jejaw ZelekeDepartment of Medical Parasitology, School of Biomedical and Laboratory Sciences, College of Medicine and Health Sciences, University of Gondar, Gondar, Ethiopia.
Eleni AyeleLeishmania Research and Treatment Center, University of Gondar Comprehensive and Specialized Hospital, Gondar, Ethiopia.
James Obondo SandeDepartment of Immunology and Molecular Biology, Makerere University, Kampala, Uganda.
Eltahir A G KhalilInstitute of Endemic Diseases, Khartoum, Sudan.
Hussam M H IbrahimInstitute of Endemic Diseases, Khartoum, Sudan.
Mahmoud A MahmoudInstitute of Endemic Diseases, Khartoum, Sudan.
Ahmed I B ZakariaInstitute of Endemic Diseases, Khartoum, Sudan.
Brenda AdikoDepartment of Immunology and Molecular Biology, Makerere University, Kampala, Uganda.
Peter O'TooleBioSciences Technology Facility, Dept of Biology, University of York, York, United Kingdom.
Flavia D'AlessioEuropean Vaccine Initiative, Heidelberg, Germany.
Charles J N LaceyYork Biomedical Research Institute, Hull York Medical School, University of York, York, United Kingdom.
Jane MbuiCenter for Clinical Research, Kenya Medical Research Institute, Nairobi, Kenya.
Asrat M HailuDepartment of Medical Parasitology, School of Biomedical and Laboratory Sciences, College of Medicine and Health Sciences, University of Gondar, Gondar, Ethiopia.
Paul M KayeYork Biomedical Research Institute, Hull York Medical School, University of York, York, United Kingdom.ORCID https://orcid.org/0000-0002-8796-4755
Margaret MbuchiCenter for Clinical Research, Kenya Medical Research Institute, Nairobi, Kenya.
Ahmed M MusaInstitute of Endemic Diseases, Khartoum, Sudan.
Joseph OloboDepartment of Immunology and Molecular Biology, Makerere University, Kampala, Uganda.
Immstat@Cure Consortium

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundVisceral leishmaniasis (VL) is the most severe form of leishmaniasis, with East Africa accounting for ~70% of global burden. It primarily affects malnourished children, young adults, and HIV co-infected individuals. Clinical outcomes range from asymptomatic to fatal, with relapse mostly linked to HIV co-infection, splenomegaly, high parasite load, poor immune responses, and elevated IgG1 concentration. In rodent VL models, systemic immune and metabolic abnormalities persist at the end of the drug treatment regime. However, the immune status of VL patients in East Africa at the end of treatment is not fully understood. METHODOLOGY/PRINCIPAL

findingsWe conducted ImmStat@cure, a multicentre clinical study to assess clinical and immune profiles of VL patients at admission and end of treatment (EoT) in East African countries. Clinical, haematological and inflammatory markers data were collected from patients from Ethiopia, Kenya, Sudan and Uganda on both time points and from convenience controls at a single time point. By integrating clinical data with haematological and inflammation markers, we have shown that patient clinical and inflammatory profiles varied at admission and partially reverted to healthy range at EoT. Partial least squares determination and logistic regression showed that concentrations of inflammatory markers, including soluble TNF receptors and sCD40L, consistently changed between admission and EoT in all four countries, and were associated with increased odds of hepatomegaly and splenomegaly. CONCLUSIONS/SIGNIFICANCE: The recovery of haematological parameters, alongside a reduction in systemic inflammatory markers may be indicative of successful treatment of VL in East Africa. The biomarker dynamics suggest a partial resolution of inflammation and restoration of immune homeostasis during treatment. To confirm their predictive value, these markers should be evaluated in cohorts with a larger number of patients who experience treatment failure.

Indexed as

Antiprotozoal AgentsBiomarkersInflammationLeishmaniasis, VisceralAdolescentAdultAfrica, EasternChildChild, PreschoolFemaleHumansMaleTreatment OutcomeYoung AdultAntiprotozoal AgentsBiomarkers

Identifiers

PMID41758879
PMCPMC12965683

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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.