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Lymphoid Cells and Tissues01:18

Lymphoid Cells and Tissues

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Articles linked to this work by shared authors, journal, and citation graph.

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Sodium stibogluconate resistance in Leishmania donovani correlates with greater tolerance to macrophage antileishmanial responses and trivalent antimony therapy.

Parasitology·2005
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Noninvasive management of Indian visceral leishmaniasis: clinical application of diagnosis by K39 antigen strip testing at a kala-azar referral unit.

Clinical infectious diseases : an official publication of the Infectious Diseases Society of America·2002
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Immunochromatographic strip-test detection of anti-K39 antibody in Indian visceral leishmaniasis.

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In vivo Imaging of Transgenic Leishmania Parasites in a Live Host
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Published on: July 27, 2010

Tissue granuloma structure-function in experimental visceral leishmaniasis.

H W Murray1

  • 1Department of Medicine, Weill College of Cornell University, New York 10021, USA. hwmurray@med.cornell.edu

International Journal of Experimental Pathology
|November 13, 2001
PubMed
Summary

Visceral leishmaniasis resistance in mice depends on T cells and macrophages forming granulomas. Studies reveal diverse granuloma structures, some ineffective, some enhancing parasite killing, and others with no visible tissue reaction.

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Area of Science:

  • Immunology
  • Parasitology
  • Cell Biology

Background:

  • Experimental visceral leishmaniasis (VL) in mice involves Leishmania donovani, a protozoan parasite.
  • Resistance to L. donovani relies on T cells, Th1 cytokine production, and activated macrophages.
  • Mature hepatic granulomas, composed of Kupffer cells, T cells, and monocytes, are crucial for controlling L. donovani infection.

Purpose of the Study:

  • To review known structure-function relationships of granulomas in experimental VL.
  • To illustrate the spectrum of granuloma responses beyond effective anti-leishmanial function.
  • To explore how different granuloma structures impact parasite control.

Main Methods:

  • Experimental modification of visceral leishmaniasis models in mice (BALB/c, C57BL/6).
  • Histological and functional analysis of hepatic granulomas.
  • Assessment of Leishmania donovani parasite burden and host immune responses.

Main Results:

  • Identified seven distinct granuloma structure-function relationships in L. donovani infection.
  • Demonstrated 'ineffective' granulomas with intact structure but no anti-parasitic function.
  • Observed 'hypertrophied' granulomas with enhanced parasite killing and 'invisible' granulomas with effective activity but no tissue reaction.

Conclusions:

  • Granuloma structure in visceral leishmaniasis is highly variable and dictates anti-parasitic function.
  • The relationship between granuloma morphology and host defense is complex and multifaceted.
  • Understanding these diverse granuloma responses is key to developing effective treatments for leishmaniasis.