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A Review: The Current in Vivo Models for the Discovery and Utility of New Anti-Leishmanial Drugs Targeting Cutaneous Leishmaniasis Publisher Pubmed



Mears ER1, 2 ; Modabber F3, 4 ; Don R3 ; Johnson GE1
Authors
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Authors Affiliations
  1. 1. College of Medicine, Swansea University, Swansea, United Kingdom
  2. 2. School of Biological Sciences, The University of Auckland, Auckland, New Zealand
  3. 3. Drugs for Neglected Diseases initiative, Geneva, Switzerland
  4. 4. Center for Research and Training on Skin Diseases and Leprosy (CRTSDL), Tehran University Medical Sciences, Tehran, Iran

Source: PLoS Neglected Tropical Diseases Published:2015


Abstract

The current in vivo models for the utility and discovery of new potential anti-leishmanial drugs targeting Cutaneous Leishmaniasis (CL) differ vastly in their immunological responses to the disease and clinical presentation of symptoms. Animal models that show similarities to the human form of CL after infection with Leishmania should be more representative as to the effect of the parasite within a human. Thus, these models are used to evaluate the efficacy of new anti-leishmanial compounds before human clinical trials. Current animal models aim to investigate (i) host–parasite interactions, (ii) pathogenesis, (iii) biochemical changes/pathways, (iv) in vivo maintenance of parasites, and (v) clinical evaluation of drug candidates. This review focuses on the trends of infection observed between Leishmania parasites, the predictability of different strains, and the determination of parasite load. These factors were used to investigate the overall effectiveness of the current animal models. The main aim was to assess the efficacy and limitations of the various CL models and their potential for drug discovery and evaluation. In conclusion, we found that the following models are the most suitable for the assessment of anti-leishmanial drugs: L. major–C57BL/6 mice (or–vervet monkey, or–rhesus monkeys), L. tropica–CsS-16 mice, L. amazonensis–CBA mice, L. braziliensis–golden hamster (or–rhesus monkey). We also provide in-depth guidance for which models are not suitable for these investigations. © 2015 Mears et al.