Drug resistance and treatment failure in leishmaniasis: A 21st century challenge

PLoS Negl Trop Dis. 2017 Dec 14;11(12):e0006052. doi: 10.1371/journal.pntd.0006052. eCollection 2017 Dec.

Abstract

Reevaluation of treatment guidelines for Old and New World leishmaniasis is urgently needed on a global basis because treatment failure is an increasing problem. Drug resistance is a fundamental determinant of treatment failure, although other factors also contribute to this phenomenon, including the global HIV/AIDS epidemic with its accompanying impact on the immune system. Pentavalent antimonials have been used successfully worldwide for the treatment of leishmaniasis since the first half of the 20th century, but the last 10 to 20 years have witnessed an increase in clinical resistance, e.g., in North Bihar in India. In this review, we discuss the meaning of "resistance" related to leishmaniasis and discuss its molecular epidemiology, particularly for Leishmania donovani that causes visceral leishmaniasis. We also discuss how resistance can affect drug combination therapies. Molecular mechanisms known to contribute to resistance to antimonials, amphotericin B, and miltefosine are also outlined.

Publication types

  • Review

MeSH terms

  • Amphotericin B / pharmacology
  • Amphotericin B / therapeutic use
  • Antiprotozoal Agents / pharmacology
  • Antiprotozoal Agents / therapeutic use
  • Drug Resistance*
  • Drug Therapy, Combination
  • Humans
  • Leishmania / drug effects*
  • Leishmania / genetics
  • Leishmania / pathogenicity*
  • Leishmania donovani / drug effects
  • Leishmania donovani / pathogenicity
  • Leishmaniasis / drug therapy*
  • Leishmaniasis / immunology
  • Leishmaniasis / parasitology
  • Leishmaniasis, Cutaneous / drug therapy
  • Leishmaniasis, Visceral / drug therapy
  • Leishmaniasis, Visceral / parasitology
  • Molecular Epidemiology
  • Phosphorylcholine / analogs & derivatives
  • Phosphorylcholine / pharmacology
  • Phosphorylcholine / therapeutic use
  • Treatment Failure

Substances

  • Antiprotozoal Agents
  • Phosphorylcholine
  • miltefosine
  • Amphotericin B