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Cutaneous Leishmaniasis in the Dorsal Skin of Hamsters: a Useful Model for the Screening of Antileishmanial Drugs
Published on: April 21, 2012
An update on pharmacotherapy for leishmaniasis.
Shyam Sundar1, Jaya Chakravarty
1Banaras Hindu University, Institute of Medical Sciences, Department of Medicine , Varanasi , India +91 542 2369632 ; drshyamsundar@hotmail.com.
Treating leishmaniasis is difficult due to limited, toxic drugs. New single-dose or combination therapies are urgently needed, especially for visceral leishmaniasis (VL) in the Indian subcontinent and for cutaneous leishmaniasis (CL).
Area of Science:
- Parasitology
- Tropical Medicine
- Pharmacology
Background:
- Leishmaniasis presents as visceral (VL), cutaneous (CL), and mucocutaneous forms.
- Current treatments for leishmaniasis are limited, toxic, and require long durations.
- Drug resistance and toxicity pose significant challenges in leishmaniasis management.
Purpose of the Study:
- To review current treatment strategies for leishmaniasis.
- To identify areas for improvement in leishmaniasis therapy.
- To highlight the need for novel treatment approaches.
Main Methods:
- Literature search conducted on PubMed focusing on leishmaniasis treatment.
- Analysis of treatment regimens for VL and CL in different geographical regions.
- Evaluation of drug combinations and single-dose therapies.
Main Results:
- Single-dose liposomal amphotericin B (L-AmB) and combination therapies are preferred for VL in the Indian subcontinent.
- Specific regimens are recommended for East African VL, Mediterranean, and South American VL.
- CL treatment decisions depend on lesion severity, species, and mucosal involvement risk.
Conclusions:
- Urgent implementation of single-dose L-AmB or combination therapy is needed for the Indian subcontinent.
- Shorter, more acceptable regimens are required for post-kala-azar dermal leishmaniasis.
- Combination therapy with new drugs requires testing in Africa; local treatment is preferred for New World CL without mucosal risk.
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