Persistent myeloid cell reprogramming despite miltefosine treatment in leishmania-infected macaques

Visceral leishmaniasis (VL) is a neglected tropical disease caused by protozoan parasites. An inflammatory immune response, associated with tissue injury, occurs shortly after infection. Using a rhesus macaque model of VL, we evaluated the impact of miltefosine therapy administered during the acute phase of infection. Despite therapy, parasites persist in multiple tissues, including the spleen, bone marrow, peripheral, and mesenteric lymph nodes. Parasite burden inversely correlates with cellular miltefosine levels. Notably, <i>L. infantum</i> remains detectable three months post-treatment. Single-cell transcriptomic analysis reveals cellular heterogeneity and reprogramming of splenic myeloid cells post-treatment, including inflammatory macrophages, immature plasmacytoid dendritic cells, and type 2 dendritic cells (DCs). Flow cytometric sorting of splenic neutrophils, macrophages, and DCs confirms the presence of <i>L. infantum</i> post-treatment, highlighting the challenge of parasite clearance. Our findings reveal a disrupted innate immune landscape post-infection that persists after treatment, indicating myeloid cell reprogramming may sustain chronic infection and parasite persistence.

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Journal
iScience
Published
2025-11-05
DOI
https://doi.org/10.1016/j.isci.2025.113900
Primary Topic
Research on Leishmaniasis Studies
Type
article
Field-Weighted Citation Impact
0.00
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article

Persistent myeloid cell reprogramming despite miltefosine treatment in leishmania-infected macaques

Jane MacDougall, Ouafa Zghidi‐Abouzid, Jérôme Estaquier, Ricardo Silvestre et al.
iScience
Research on Leishmaniasis Studies
article

Persistent myeloid cell reprogramming despite miltefosine treatment in leishmania-infected macaques

Jane MacDougall, Ouafa Zghidi‐Abouzid, Jérôme Estaquier, Ricardo Silvestre, Yasmina Fortier, Julien Clain, Chloé Borde, Maria Paola Costi, Calaiselvy Soundaramourty, Arnaud Droit, Charles Joly-Beauparlant, Anabela Cordeiro‐da‐Silva, Vasco Rodrigues, Gina Racine, Alain Pruvost, Steven Boutrais, Sónia André, Morgane Picard
article en

Abstract

Visceral leishmaniasis (VL) is a neglected tropical disease caused by protozoan parasites. An inflammatory immune response, associated with tissue injury, occurs shortly after infection. Using a rhesus macaque model of VL, we evaluated the impact of miltefosine therapy administered during the acute phase of infection. Despite therapy, parasites persist in multiple tissues, including the spleen, bone marrow, peripheral, and mesenteric lymph nodes. Parasite burden inversely correlates with cellular miltefosine levels. Notably, <i>L. infantum</i> remains detectable three months post-treatment. Single-cell transcriptomic analysis reveals cellular heterogeneity and reprogramming of splenic myeloid cells post-treatment, including inflammatory macrophages, immature plasmacytoid dendritic cells, and type 2 dendritic cells (DCs). Flow cytometric sorting of splenic neutrophils, macrophages, and DCs confirms the presence of <i>L. infantum</i> post-treatment, highlighting the challenge of parasite clearance. Our findings reveal a disrupted innate immune landscape post-infection that persists after treatment, indicating myeloid cell reprogramming may sustain chronic infection and parasite persistence.

iScienceVol. 28(12)
University of Modena and Reggio Emilia (IT), Inserm (FR), Universidade do Porto (PT), Université Paris Cité (FR), Commissariat à l'Énergie Atomique et aux Énergies Alternatives (FR), Université Paris-Saclay (FR), Institut National de Recherche pour l'Agriculture, l'Alimentation et l'Environnement (FR), CEA Paris-Saclay (FR), Institut de recherches économiques et sociales (FR), i3S - Instituto de Investigação e Inovação em Saúde, Universidade do Porto (PT), Université Laval (CA), University of Minho (PT)
Openalex Percentile: Top 57%
Research on Leishmaniasis Studies
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