Antiprotozoal Drugs
Amoebiasis, Giardiasis, Leishmaniasis & Trypanosomiasis — Agents, Mechanisms, Resistance & Recent Advances
Past MUHS · 1
MUHSSummer '21
Introduction & scope
- Antiprotozoal (non-malarial) drugs — agents against pathogenic human protozoa other than Plasmodium — Entamoeba histolytica (amoebiasis), Giardia lamblia (giardiasis), Trichomonas vaginalis (trichomoniasis), Leishmania spp. (kala-azar), Trypanosoma spp. (sleeping sickness, Chagas) and Toxoplasma gondii.
- Why they matter — no effective vaccines exist, so chemotherapy is the only means to treat and to reduce transmission; many protozoa cause severe/opportunistic disease in the immunosuppressed (HIV/AIDS, transplant) — leishmaniasis, cryptosporidiosis and toxoplasmosis are recognised AIDS-associated infections.
- Indian burden — amoebiasis is endemic across most of India (~15% infected); India, with Bihar as the epicentre, carries a large share of the world's visceral leishmaniasis — Bihar alone ~50% of global VL — driving distinctive Indian treatment policy.
- Central problem — many antiprotozoals are toxic at therapeutic doses and drug resistance is rising (antimony-resistant kala-azar, metronidazole-resistant Trichomonas, melarsoprol resistance).
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Antiprotozoal Drugs
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