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Updated: Aug 21, 2026

In vivo Imaging of Transgenic Leishmania Parasites in a Live Host
Published on: July 27, 2010
[Effects of cytokine-activated macrophages on intracellular leishmania]
Abstract:
The effects of activated macrophages on Leishmania donovani amastigotes and nitrite (NO2-) release were determined by in vitro inducement of macrophage activation with recombinant IFN-r, TNF-alpha, and rIL-3. The results indicated that rIFN-r or rTNF-alpha at 40,000U/L was able to induce a significant but modest level of macrophage activity, and synergistic effect of rIFN-r and rTNF-alpha was apparent in the induction of macrophage activation. 48 hours after macrophages were induced with both rIFN-r and rTNF-alpha, the percentage of the macrophages infected by Leishmania donovani was 16%, and the mean number of the parasite per infected macrophage was 1.2 +/- 0.04. There was a strikingly significant difference in comparison with the control group, in which the infection rate of macrophages was 62% and the mean number of the parasite per infected macrophage was 6.8 +/- 0.10. However, no significant difference was noted between rIL-3 at 1/100 concentration, alone or combined with rIFN-r, and the control in leishmanicidal activity of macrophages. An increase of NO2- in the culture supernatants was paralleled by the ability of various cytokine-activated macrophages to kill the intracellular parasites.
Insights
Recombinant IFN-γ or TNF-α activates macrophages to combat Leishmania donovani, reducing parasite load. This cytokine-induced macrophage activation offers a potential strategy against leishmaniasis.
Area of Science:
- Immunology
- Parasitology
Context:
- Leishmania donovani is a protozoan parasite that causes leishmaniasis, a neglected tropical disease.
- Macrophages play a crucial role in the host immune response against Leishmania donovani.
Purpose:
- To investigate the in vitro effects of recombinant interferon-gamma (IFN-γ), tumor necrosis factor-alpha (TNF-α), and interleukin-3 (IL-3) on macrophage activation and their leishmanicidal activity against Leishmania donovani amastigotes.
Summary:
- Recombinant IFN-γ or TNF-α, particularly when used synergistically, significantly enhanced macrophage activity and leishmanicidal capacity against Leishmania donovani amastigotes in vitro.
- Activated macrophages showed a reduced infection rate (16%) and parasite burden (1.2 parasites/macrophage) compared to control (62% infection, 6.8 parasites/macrophage).
- Nitrite (NO2-) release in culture supernatants correlated with the enhanced ability of cytokine-activated macrophages to kill intracellular parasites, while IL-3 alone or with IFN-γ did not show significant leishmanicidal effects.
Impact:
- This study highlights the potential of IFN-γ and TNF-α in modulating macrophage function for controlling Leishmania donovani infection.
- The findings suggest that cytokine-based therapies could be explored for treating leishmaniasis.
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