Skip to content


BMC Proceedings

Open Access

Do scars caused by past history of Leishmania major Ainfection may harbor persistent parasites?

  • Rabiaa Manel Sghaier1, 3,
  • Fouad Benhnini1, 3,
  • Amor Zaatour2, 3,
  • Hanène Attia1, 3,
  • Ghada Mkannez1, 3,
  • Aymen Bali1, 3,
  • Fatma Zahra Guerfali1, 3,
  • Afif Ben-Salah2, 3,
  • Dhafer Laouini1, 3 and
  • Koussay Dellagi1, 3
BMC Proceedings20115(Suppl 1):P42

Published: 10 January 2011


LeishmaniasisDrain Lymph NodeCutaneous LeishmaniasisEnrich MediumDisease Reactivation

Based on the knowledge that a cured infection protects the individual from re-infection, the development of a vaccine to prevent leishmaniasis has been a goal for nearly a century. Indeed, it is generally believed that after healing of leishmaniasis, sterile cure is never achieved and that few residual living parasites will remain sequestered within some host cells that offer them a safe shelter and hence maintain anti-parasite immune memory. This statement is mainly supported by data from experimental leishmaniasis in mice of susceptible or resistant phenotype, in which, live parasites could be recovered from lesions even after healing, and in which disease reactivation can be obtained by immune manipulation even after apparent complete cure.

Whether maintenance of a long-term immune effector memory in humans will also require persistence of live parasites is presently unknown but is very important in the perspective of a vaccine development. Our aim herein was to address the issue of Leishmania major parasite persistence vs. sterile healing in zoonotic cutaneous leishmaniasis (ZCL) by analyzing biopsies of scars from healed volunteers.

Skin-punch scars’ biopsies (n=59, range of scar age: 1–5 years) have been obtained from volunteers (18–55 years old) living in two ZCL endemic foci, who had a confirmed past history, are clinically cured of ZCL and who gave their written consent. The whole protocol was approved by the local IRB. The specimens were taken under sterile conditions and local anaesthesia. Each specimen was divided into three parts: (i) the first sample was processed for quantitative real time PCR, (ii) the second was cultured in vitro in enriched medium and (iii) the third was inoculated into the footpad of susceptible BALB/c mice which were kept under observation for five months.

For in vitro isolation and after microscopic observation for at least 8 weeks, all cultures were found negative. For in vivo isolation, biopsy-inoculated mice were killed five months later, and skin fragments, draining lymph nodes and spleen were inoculated into culture medium, observed carefully for at least 8 weeks before being also designated as negative. PCR results were found negative for the majority of biopsies. These results indicate that any potential persistent living parasites after cure are unlikely to be sequestered in ZCL scars. This issue is of importance in strategies for control of leishmaniasis and requires further discussion.



Supported by Grant #5P50AI074178 from NIH/NIAID.

Authors’ Affiliations

Laboratory of Immuno-Pathology, Vaccinology and Molecular Genetics, Institut Pasteur de Tunis, Tunis-Belvedere, Tunisia
Laboratory of Medical Epidemiology, Institut Pasteur de Tunis, Tunis-Belvedere, Tunisia
WHO Collaborating Center for Research and Training in Leishmaniasis, Institut Pasteur de Tunis, Tunis-Belvedere, Tunisia


© Sghaier et al; licensee BioMed Central Ltd. 2011

This article is published under license to BioMed Central Ltd. This is an open access article distributed under the terms of the Creative Commons Attribution License (, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.