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DOI 10.3390/ijms27073055

Медицинская библиотека · International journal of molecular sciences · 2026

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

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

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Аннотация

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.

Для цитирования: Melcón-Fernández Estela, Balaña-Fouce Rafael, García-Estrada Carlos, Reguera Rosa M, Fernández-Rubio Celia, Cendón-Álvarez Marta, Pérez-Pertejo Yolanda. Antileishmanial and Immunomodulatory Activity of Paclitaxel and Docetaxel Combined with Miltefosine and Paromomycin.. International journal of molecular sciences. 2026. DOI: 10.3390/ijms27073055.

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