Abstract
Mectizan (Ivermectin) has been proved to be central to the control of onchoceriasis through self-sustainable community-based treatment. The possibility of parasitological unresponsiveness to this treatment or selection for drug resistance has emerged recently in many occasions. The reason for the reduced ability of Mectizan to maintain low levels of dermal microfilariae and early recurrent pruritus can only be speculated upon. Here, we report our own findings to address this particular issue.
MeSH terms
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Animals
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Antigens, Helminth / immunology
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Antinematodal Agents / therapeutic use*
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Cohort Studies
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Filaricides / pharmacology
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Filaricides / therapeutic use
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Humans
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Immunocompetence
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Ivermectin / therapeutic use*
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Leukocytes, Mononuclear / immunology
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Lymphocyte Activation
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Microfilariae / isolation & purification
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Onchocerca volvulus* / immunology
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Onchocerciasis / drug therapy*
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Onchocerciasis / immunology
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Onchocerciasis / pathology
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Pruritus / drug therapy*
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Pruritus / immunology
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Pruritus / pathology
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Recurrence
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Sudan / ethnology
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Treatment Outcome
Substances
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Antigens, Helminth
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Antinematodal Agents
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Filaricides
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Ivermectin