Evidence map›Paper›PMID 41977242›Full record

ArticleInternational journal of molecular sciences2026

Antileishmanial and Immunomodulatory Activity of Paclitaxel and Docetaxel Combined with Miltefosine and Paromomycin.

Estela Melcón-Fernández, Rafael Balaña-Fouce, Carlos García-Estrada, Rosa M Reguera, Celia Fernández-Rubio, Marta Cendón-Álvarez, Yolanda Pérez-Pertejo

Abstract read
In one paragraph

Article in International journal of molecular sciences, 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

7 authors.

Estela Melcón-FernándezDepartamento de Ciencias Biomédicas, Facultad de Veterinaria, Universidad de León, 24071 León, Spain.ORCID 0000-0002-9663-060X
Rafael Balaña-FouceDepartamento de Ciencias Biomédicas, Facultad de Veterinaria, Universidad de León, 24071 León, Spain.ORCID 0000-0003-0418-6116
Carlos García-EstradaDepartamento de Ciencias Biomédicas, Facultad de Veterinaria, Universidad de León, 24071 León, Spain.ORCID 0000-0001-5617-9669
Rosa M RegueraDepartamento de Ciencias Biomédicas, Facultad de Veterinaria, Universidad de León, 24071 León, Spain.ORCID 0000-0001-9148-2997
Celia Fernández-RubioDepartamento de Ciencias Biomédicas, Facultad de Veterinaria, Universidad de León, 24071 León, Spain.ORCID 0000-0001-5254-8121
Marta Cendón-ÁlvarezDepartamento de Ciencias Biomédicas, Facultad de Veterinaria, Universidad de León, 24071 León, Spain.ORCID 0009-0007-2001-6041
Yolanda Pérez-PertejoDepartamento de Ciencias Biomédicas, Facultad de Veterinaria, Universidad de León, 24071 León, Spain.ORCID 0000-0003-2361-3785

Funding

Dirección General de Universidades e Investigación Junta de Castilla y León LE017-G24
6 · The paper itself

Abstract

A wide range of Leishmania species, transmitted by phlebotomine, cause leishmaniasis, which presents diverse clinical manifestations. Leishmaniasis has a high impact on vulnerable communities, primarily affecting people suffering from malnutrition or poor housing. Because leishmaniasis is associated with poverty, access to treatment is limited. In addition, high drug toxicity and therapeutic failure, related to drug resistance, remain major challenges. Therefore, there is a need to develop new therapeutic approaches that are safer and more effective. Drug combinations and repurposing are two strategies used in the development of treatments. The combination of drugs with different mechanisms of action can minimise resistance and allow dose reduction, increasing the likelihood of successful drug repurposing. This study evaluated the antileishmanial effects of combining antitumoral agents (paclitaxel and docetaxel) with standard drugs (miltefosine and paromomycin). Results demonstrated synergistic effects at higher doses. Furthermore, the antitumoral compounds enhanced the host immune response by promoting macrophage polarisation toward the M1 phenotype, essential for parasite control. These findings highlight a promising approach that could improve efficacy and reduce resistance.

Indexed as

Antiprotozoal AgentsDocetaxelImmunologic FactorsLeishmaniaLeishmaniasisPaclitaxelParomomycinPhosphorylcholineAnimalsDrug SynergismHumansMacrophagesMiceAntiprotozoal AgentsDocetaxelImmunologic FactorsmiltefosinePaclitaxelParomomycinPhosphorylcholinecytokinesdocetaxeldrug combinationsdrug repurposingleishmaniasismiltefosinepaclitaxelparomomycin

Identifiers

PMID41977242
PMCPMC13073897

What OpenQuestion holds

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LicenceCC BY
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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.