Chemotherapeutics of visceral leishmaniasis: present and future developments

Parasitology. 2018 Apr;145(4):481-489. doi: 10.1017/S0031182017002116. Epub 2017 Dec 7.

Abstract

Treatment of Visceral Leishmaniasis (VL), a neglected tropical disease, is very challenging with few treatment options. Long duration of treatment and drug toxicity further limit the target of achieving VL elimination. Chemotherapy remains the treatment of choice. Single dose of liposomal amphotericin B (LAmB) and multidrug therapy (LAmB + miltefosine, LAmB + paromomycin (PM), or miltefosine + PM) are recommended treatment regimen for treatment of VL in Indian sub-continent. Combination therapy of pentavalent antimonials (Sbv) and PM in East Africa and LAmB in the Mediterranean region/South America remains the treatment of choice. Various drugs having anti-leishmania properties are in preclinical phase and need further development. An effective treatment and secondary prophylaxis of HIV-VL co-infection should be developed to decrease treatment failure and drug resistance.

Keywords: Amphoterecin B; Kala-Azar; Miltefosine; Paromomycin; Visceral leishmaniasis.

Publication types

  • Research Support, N.I.H., Extramural
  • Review

MeSH terms

  • Amphotericin B / pharmacology
  • Amphotericin B / therapeutic use
  • Amphotericin B / toxicity
  • Animals
  • Antiprotozoal Agents / adverse effects
  • Antiprotozoal Agents / pharmacology
  • Antiprotozoal Agents / therapeutic use*
  • Antiprotozoal Agents / toxicity
  • Clinical Trials as Topic
  • Drug Resistance, Multiple
  • Drug Therapy, Combination
  • HIV Infections / drug therapy
  • HIV Infections / parasitology
  • Humans
  • India / epidemiology
  • Leishmania donovani / drug effects*
  • Leishmaniasis, Visceral / drug therapy*
  • Leishmaniasis, Visceral / epidemiology
  • Meglumine Antimoniate / administration & dosage
  • Meglumine Antimoniate / adverse effects
  • Meglumine Antimoniate / therapeutic use
  • Paromomycin / pharmacology
  • Paromomycin / therapeutic use
  • Paromomycin / toxicity
  • Phosphorylcholine / analogs & derivatives
  • Phosphorylcholine / pharmacology
  • Phosphorylcholine / therapeutic use
  • Phosphorylcholine / toxicity
  • Psychodidae / parasitology
  • Sheep
  • South America / epidemiology
  • Treatment Outcome*

Substances

  • Antiprotozoal Agents
  • Phosphorylcholine
  • miltefosine
  • Paromomycin
  • Meglumine Antimoniate
  • Amphotericin B