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In vivo Imaging of Transgenic Leishmania Parasites in a Live Host
Published on: July 27, 2010
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Leishmaniasis and IFN-γ dependent chemokines
P Fallahi1, G Elia2, A Bonatti1
1Department of Clinical and Experimental Medicine, University of Pisa, Pisa.
La Clinica Terapeutica
|November 16, 2016
Summary
Interferon-gamma-induced protein (IP)-10 plays a crucial role in the immune response to Leishmaniasis. Higher IP-10 levels correlate with disease severity but also indicate a protective immune response, suggesting therapeutic potential.
Area of Science:
- Immunology
- Infectious Diseases
- Parasitology
Background:
- Leishmaniasis is a significant global health concern caused by Leishmania parasites, transmitted by sandflies, affecting millions worldwide.
- The disease manifests in three forms: Cutaneous (CL), Mucocutaneous, and Visceral Leishmaniasis (VL), with VL having a substantial incidence.
- Immune responses involving cytokines and chemokines, particularly Interferon-gamma (IFN-γ) and its dependent chemokines, are critical in mediating host defense against Leishmania infection.
Purpose of the Study:
- To investigate the role of Interferon-gamma-induced protein (IP)-10 in the immune response to Leishmaniasis.
- To explore the correlation between IP-10 expression, disease severity, and host-protective immunity in Leishmaniasis patients.
- To evaluate the potential of IP-10 as a therapeutic target for Leishmaniasis.
Main Methods:
- Analysis of skin biopsies from Cutaneous Leishmaniasis patients to assess IP-10 expression in lesions.
- Detection of IP-10 and its receptor (CXCR3) expression in monocytes following Leishmania infection.
- Evaluation of IP-10's role in host-protective immunity during vaccination models against Leishmania infection.
Main Results:
- Higher expression of IP-10 was observed in recent CL lesions compared to late lesions.
- Enhanced IP-10 and CXCR3 expression was predominantly found in CD14(+) monocytes after L. braziliensis infection, potentially increasing disease severity.
- IP-10 was associated with a strong T helper cell type 1 (Th1) immune response and conferred protection against Visceral Leishmaniasis, with high clinical scores correlating positively with IP-10 expression.
Conclusions:
- IP-10 is a key mediator in the immune response to Leishmaniasis, influencing both disease progression and protective immunity.
- IP-10's role in cellular recruitment and its association with Th1 responses highlight its significance in combating Leishmania infection.
- Further research into IP-10's function in Leishmaniasis is warranted to explore its potential as a therapeutic target.

