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1.
Am J Trop Med Hyg ; 103(3): 1135-1142, 2020 09.
Artículo en Inglés | MEDLINE | ID: mdl-32588807

RESUMEN

Wambabya-Rwamarongo onchocerciasis focus is one of the eight foci Uganda verified using the WHO verification guidelines. The approach for elimination was twice yearly treatment with ivermectin for every round, treating at least 90% of all the eligible population. This was in combination with vector elimination using Abate® (BASF SE, Limburgerhof, Germany) since elimination nationwide policy was launched. From 2008 to 2013, the program distributed ivermectin with a mean treatment coverage of the ultimate treatment goal (UTG) or eligible population of 91.2%, with a range of 85-96%. In 2009, vector elimination based on ground larviciding had a dramatic impact on the Simulium vectors, as the last fly was observed in October 2009. No more Simulium vectors were observed during a period of at least 7 years, including the 3-year posttreatment surveillance (PTS) until the focus was reclassified as eliminated in August 2017. During the PTS period, none of the 10,578 trapped crabs were found infested with the aquatic stages of the vector. The last infested crab was observed in March 2010, and for at least 7 years, no infested crabs were observed. Serological surveys showed that of 2,978 young children examined in 2013, only one was OV16 positive (0.0%; 95% CI: 0-0.21). In 2017, after the PTS period, all 3,079 young children examined were negative for OV16 (95% CI: 0-0.16). Therefore, entomological and serological results provided evidence that resulted in the reclassification of Wambabya-Rwamarongo focus from "transmission interrupted" to "transmission eliminated" with no possibility of recrudescence.


Asunto(s)
Antiparasitarios/uso terapéutico , Braquiuros/parasitología , Ivermectina/uso terapéutico , Oncocercosis/epidemiología , Simuliidae/parasitología , Temefós/uso terapéutico , Animales , Erradicación de la Enfermedad , Humanos , Oncocercosis/parasitología , Oncocercosis/transmisión , Uganda/epidemiología
2.
PLoS Negl Trop Dis ; 10(6): e0004772, 2016 06.
Artículo en Inglés | MEDLINE | ID: mdl-27300294

RESUMEN

BACKGROUND: A homologue of the ecdysone receptor has previously been identified in human filarial parasites. As the ecdysone receptor is not found in vertebrates, it and the regulatory pathways it controls represent attractive potential chemotherapeutic targets. METHODOLOGY/ PRINCIPAL FINDINGS: Administration of 20-hydroxyecdysone to gerbils infected with B. malayi infective larvae disrupted their development to adult stage parasites. A stable mammalian cell line was created incorporating the B. malayi ecdysone receptor ligand-binding domain, its heterodimer partner and a secreted luciferase reporter in HEK293 cells. This was employed to screen a series of ecdysone agonist, identifying seven agonists active at sub-micromolar concentrations. A B. malayi ecdysone receptor ligand-binding domain was developed and used to study the ligand-receptor interactions of these agonists. An excellent correlation between the virtual screening results and the screening assay was observed. Based on both of these approaches, steroidal ecdysone agonists and the diacylhydrazine family of compounds were identified as a fruitful source of potential receptor agonists. In further confirmation of the modeling and screening results, Ponasterone A and Muristerone A, two compounds predicted to be strong ecdysone agonists stimulated expulsion of microfilaria and immature stages from adult parasites. CONCLUSIONS: The studies validate the potential of the B. malayi ecdysone receptor as a drug target and provide a means to rapidly evaluate compounds for development of a new class of drugs against the human filarial parasites.


Asunto(s)
Ecdisona/metabolismo , Ecdisterona/análogos & derivados , Filariasis/tratamiento farmacológico , Hidrazinas/farmacología , Receptores de Esteroides/agonistas , Aminoácidos Diaminos/administración & dosificación , Animales , Brugia Malayi/efectos de los fármacos , Brugia Malayi/aislamiento & purificación , Descubrimiento de Drogas , Evaluación Preclínica de Medicamentos , Ecdisterona/química , Ecdisterona/farmacología , Filariasis/parasitología , Gerbillinae , Células HEK293 , Humanos , Hidrazinas/química , Hidrazinas/aislamiento & purificación , Larva/efectos de los fármacos , Ligandos , Modelos Moleculares , Simulación del Acoplamiento Molecular , Receptores de Esteroides/metabolismo
3.
Am J Trop Med Hyg ; 89(2): 293-300, 2013 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-23690555

RESUMEN

The objective of the study was to determine whether annual ivermectin treatment in the Nyagak-Bondo onchocerciasis focus could safely be withdrawn. Baseline skin snip microfilariae (mf) and nodule prevalence data from six communities were compared with data collected in the 2011 follow-up in seven communities. Follow-up mf data in 607 adults and 145 children were compared with baseline (300 adults and 58 children). Flies collected in 2011 were dissected, and poolscreen analysis was applied to ascertain transmission. Nodule prevalence in adults dropped from 81.7% to 11.0% (P < 0.0001), and mf prevalence dropped from 97.0% to 23.2% (P < 0.0001). In children, mf prevalence decreased from 79.3% to 14.1% (P < 0.0001). Parous and infection rates of 401 flies that were dissected were 52.9% and 1.5%, respectively, whereas the infective rate on flies examination by polymerase chain reaction (PCR) was 1.92% and annual transmission potential was 26.9. Stopping ivermectin treatment may result in onchocerciasis recrudescence.


Asunto(s)
Antiparasitarios/uso terapéutico , Ivermectina/uso terapéutico , Onchocerca volvulus/efectos de los fármacos , Oncocercosis/prevención & control , Oncocercosis/transmisión , Adulto , Animales , Antiparasitarios/administración & dosificación , Braquiuros/parasitología , Niño , Esquema de Medicación , Humanos , Insectos Vectores/parasitología , Ivermectina/administración & dosificación , Oncocercosis/epidemiología , Simuliidae/parasitología , Uganda/epidemiología
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