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Investigating the Phagocytosis of Leishmania using Confocal Microscopy
Published on: July 29, 2021
The Capsular Polysaccharides GXM and GXMGal from Cryptococcus neoformans Modulate Macrophages Infected with
Idália Maria Ferreira-Dos-Santos1, Elias Barbosa da Silva-Junior1, Afonso Santine M M Velez2
1Instituto de Biofísica Carlos Chagas Filho, Universidade Federal do Rio de Janeiro, Rio de Janeiro 21941-902, Brazil.
Abstract:
Leishmania spp. are obligatory intracellular parasites that primarily infect macrophages. The macrophage immune response plays a pivotal role in determining the control or progression of infection. "M1-like" macrophages mediate parasite clearance through the production of nitric oxide, pro-inflammatory cytokines, and reactive oxygen species, whereas "M2-like" macrophages contribute to infection progression by exerting anti-inflammatory effects. The capsular polysaccharides Glucuronoxylomannan (GXM) and glucuronoxylomannogalactan (GXMGal) from Cryptococcus neoformans are capable of immunomodulating the macrophage response. GXM exhibits immunoregulatory activity, whereas GXMGal induces a pro-inflammatory response. Although the activity of these polysaccharides has been studied in cryptococcosis, their immunomodulatory potential in other infectious models remains largely unexplored. Here, we investigated the effects of GXM and GXMGal on Leishmania major infection in murine peritoneal macrophages. Murine peritoneal macrophages were infected with L. major and, 24 h post-infection, treated with 50 μg of either GXM or GXMGal. Our data revealed that GXM treatment enhanced L. major infection, while GXMGal treatment had no significant effect on the parasitic load in infected macrophages.
Insights
Glucuronoxylomannan (GXM) from Cryptococcus neoformans worsened Leishmania major infection in macrophages. Glucuronoxylomannogalactan (GXMGal) had no significant impact on parasitic load, suggesting differential immunomodulatory effects.
Area of Science:
- Immunology
- Parasitology
- Microbiology
Background:
- Leishmania spp. are intracellular parasites infecting macrophages, crucial for immune response.
- Macrophage polarization (M1 vs. M2) dictates infection control or progression.
- Cryptococcus neoformans polysaccharides GXM and GXMGal modulate macrophage responses.
Purpose of the Study:
- To investigate the immunomodulatory effects of GXM and GXMGal on Leishmania major infection.
- To explore the potential of these fungal polysaccharides in a leishmaniasis model.
Main Methods:
- Murine peritoneal macrophages were infected with Leishmania major.
- Post-infection, macrophages were treated with GXM or GXMGal.
- Parasitic load was assessed to determine treatment effects.
Main Results:
- GXM treatment significantly enhanced Leishmania major infection in macrophages.
- GXMGal treatment showed no significant effect on parasitic load.
- Fungal polysaccharides exhibit differential impacts on Leishmania infection.
Conclusions:
- GXM exacerbates Leishmania major infection, indicating a detrimental immunomodulatory role in this context.
- GXMGal does not significantly alter Leishmania major parasitic load.
- These findings highlight the complex interactions between fungal components and host immune cells during parasitic infections.
Related Concept Videos
Cryptococcal Meningitis
Leishmaniasis

