dc.date.accessioned2022-10-25T19:54:11Z
dc.date.accessioned2023-05-23T18:54:10Z
dc.date.available2022-10-25T19:54:11Z
dc.date.available2023-05-23T18:54:10Z
dc.date.created2022-10-25T19:54:11Z
dc.date.issued2001
dc.identifierhttps://hdl.handle.net/20.500.12866/12484
dc.identifierhttps://doi.org/10.1086/324161
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/6395025
dc.description.abstractTreatment failures for leishmaniasis with pentavalent antimonials, including meglumine antimonate, are increasingly common in many endemic areas. Imiquimod (Aldara; 3M Pharmaceuticals) is a novel immune response-activating compound, approved by the United States Food and Drug Administration, that is currently used to treat cervical warts and has been shown to activate macrophage killing of Leishmania species. Therefore, an open-label, prospective study was conducted of combined imiquimod plus meglumine antimonate therapy in 12 patients with cutaneous leishmaniasis who had previously not responded to meglumine antimonate therapy. All of the patients responded well to this combination therapy, and 90% were found to be cured at the 6-month follow-up period.
dc.languageeng
dc.publisherOxford University Press
dc.relationClinical Infectious Diseases
dc.relation1537-6591
dc.rightshttps://creativecommons.org/licenses/by-nc-nd/4.0/deed.es
dc.rightsinfo:eu-repo/semantics/restrictedAccess
dc.subjectDrug-Resistant
dc.subjectImiquimod
dc.subjectImmunomodulator
dc.titleSuccessful treatment of drug-resistant cutaneous leishmaniasis in humans by use of imiquimod, an immunomodulator
dc.typeinfo:eu-repo/semantics/article


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