SUMMARYThe aim of this study was to estimate the frequency of human toxocariasis in Cauday district, Cajamarca, Peru, using a dot-ELISA test. From June to October 2005, a total of 256 adult subjects were studied. Blood samples were collected for serology by a dot-ELISA test and for hematological examination. Parasitological examination was also carried out in stool samples to check cross-reactions in the dot-ELISA. The frequency observed was 44.92%, with a significant higher proportion of positivity in male subjects. From subjects with positive serology, 45.6% had respiratory symptoms, 40.44% abdominal pain, 32.35% hepatic symptoms, 14.7% cutaneous signs, 13.23% ocular manifestations, 43.38% eosinophilia, and all of these were statistically associated to serology. Among the population evaluated, 90.23% (231/256) were parasitized. From subjects with positive serology, 92.17% had at least one intestinal parasite and the most frequent were: Blastocystis hominis (68.38%), Giardia lamblia (28.68%), Hymenolepis nana (20.0%), Ascaris lumbricoides (15.65%), Entamoeba histolytica/E. dispar (13.24%), Cyclospora cayetanensis (4.41%), Cryptosporidium sp. (1.47%), Enterobius vermicularis (0.87%), Strongyloides stercoralis (0.87%), Taenia sp. (0.87%), and Trichuris trichiura (0.87%). The rate of false positives in the dot-ELISA test was improved by serum absorption each with A. suum antigens, with a decrease of cross-reactions. In conclusion, human toxocariasis is highly frequent in this population and some risk factors like dog/cat ownership, presence of pets within house, and previous history of geophagia were observed in the present study.

SUMMARYThe aim of this study was to estimate the frequency of human toxocariosis in a child population from Morrope district, Lambayeque, Peru. From October to December 2005, 182 school children (96 male and 86 female) were studied. Blood samples were collected for Toxocara ELISA-IgG test and hematological examination. Additionally, stool samples were collected for coproparasitological examination to check cross reactions. We found frequency of positives in 32.4% (59/182) with a significant higher proportion of positivity in male children (p < 0.00001). 71.2% of the children with positive serology (52 male and seven female), were between five and 10 years old, 77.96% had respiratory symptoms, 61.02% had ocular manifestations, 38.98% had hepatic symptoms, 38.98% had mild or moderate eosinophilia, signs statistically associated with seropositivity. 83.5% of studied population had some intestinal parasite, such as: Blastocystis hominis (53.3%), Giardia lamblia (31.3%), Entamoeba coli (29.1%), Entamoeba histolytica/E. dispar (1.1%), Hymenolepis nana (5.49%), and Ascaris lumbricoides (3.3%), but they had not any association with serology results. The ownership of dogs or/and cats were significantly associated with seropositivity to antiToxocara antibodies although the presence of such pets within the house was not. In conclusion, clinical and serological evidence of Toxocara infection exists in the studied population.

Human toxocarosis is an important parasitic zoonosis caused by larval stages of Toxocara species, the roundworms from dogs and cats. Larval migration through different soft tissues in the human generates several clinical entities in the patient, such as visceral larva migrans, ocular toxocarosis, and neurotoxocarosis. Definitive diagnosis by histopathological methods is very difficult or almost impossible and, nowadays, the diagnosis is usually made by clinical signs/symptoms, epidemiological background of the patient and the use of hematological and immunological tests which finally help to confirm the clinical suspicion of the illness. The purpose of this paper was to update the available knowledge on the use of different tools for both the diagnosis and following up of human toxocarosis.

SUMMARYThe aim of this study was to assess the seroprevalence of human toxocariasis in three Andean communities from the Northeast of Lima, Peru. A total of 303 subjects including children and adults were studied and blood samples were collected to detect anti-Toxocara antibodies by ELISA-IgG test and by hematological examination; stool samples were collected also for parasitological examination. The overall seroprevalence of toxocariasis observed in the total population was 20.46%, with a significant high proportion in children from one to 10 years old (p = 0.034). Among the subjects with positive serology, 32.26% of them had respiratory disturbances, 22.58% hepatomegaly, 17.74% ocular signs or symptoms, 14.51% abdominal pain, 9.68% neurological involvement, and 4.84% cutaneous signs, but none of these clinical features were associated to a positive serology by multivariate analysis. Furthermore, 79.03% of seropositive subjects also harbored at least one intestinal parasite, which was associated to a positive serology (p < 0.05). The presence of pets within the houses, a previous history of pica or geophagia and the use of public places were also present in this population, but only the latter was associated to the serology (p < 0.05). In conclusion, clinical, serological, and epidemiological evidences for larval Toxocara infection were found in the studied population.

La toxocarosis humana es una importante zoonosis parasitaria causada por formas larvarias de especies del género Toxocara, un parásito nematodo de los perros y los gatos. La migración de la larva por los diferentes tejidos blandos en el ser humano genera una serie de entidades clínicas en el paciente, tales como el síndrome de larva migrans visceral, la toxocarosis ocular y la neurotoxocarosis. El diagnóstico definitivo es mediante la histopatología en biopsias, pero resulta ser casi imposible de realizar y actualmente su diagnóstico se establece mediante el análisis de la sintomatología clínica, los antecedentes epidemiológicos del paciente y el uso de pruebas hematológicas e inmunológicas de laboratorio que son las que finalmente ayudan a confirmar la sospecha clínica de la enfermedad. El propósito del presente artículo es actualizar los conocimientos que se tienen sobre el uso de las diferentes herramientas para establecer el diagnóstico y el monitoreo de la toxocarosis humana.

Se realizó una revisión bibliográfica para actualizar y sistematizar la información existente sobre la infección humana por el género Toxocara. Se describe los mecanismos de transmisión, epidemiología, formas clínicas, métodos de diagnóstico, esquemas de tratamiento. Además, se resalta su importancia como causa infecciosa de ceguera, en población joven, que resulta potencialmente prevenible y curable mediante el diagnóstico precoz. Por lo cual, se plantea propuestas para implementar la vigilancia epidemiológica. Asimismo, algunas sugerencias para mejorar la legislación existente que permita disminuir el riesgo de la transmisión a la población en general e incrementar el conocimiento que existe sobre esta infección en nuestro país.

Objetivo: Estimar la prevalencia de la infección por coccidios intestinales en niños asintomáticos de una comunidad urbano marginal de Lima. Material y Métodos: Se recolectó muestras fecales de 79 niños asintomáticos de 7 meses a 7 años de edad del Asentamiento Humano “Las Casuarinas de Villa”. Se revisó por el método directo y se preparó frotis para la coloración con la técnica de Kinyoun. Una parte de la muestra se colocó en frascos con bicromato de potasio al 2,5% para la esporulación. Después de 10 días, se preparó frotis para colorearlos con Kinyoun. Resultados: El examen directo detectó una muestra con Cryptosporidium (1,3%); en los frotis coloreados previa esporulación se encontró 3 muestras con Cryptosporidium (3,8%) y una con Isospora belli (1,3%) y en los frotis coloreados postesporulación se detectó 6 muestras con Cryptosporidium (7,6%) y una con Isospora belli. Conclusión: La esporulación permitió aumentar la posibilidad de detectar casos con Cryptosporidium.

RESUMENOBJETIVO: Estandarizar la técnica ELISA para el diagnóstico de infección humana por Toxocara canis con antígeno excretado-secretado preparado en nuestro medio. MATERIAL Y MÉTODOS: Se colectó huevos de T. canis y se les incubó con formol (2%) a 28 o C hasta obtener larvas de tercer estadio, las que luego de ser liberadas fueron incubadas en RPMI a 37°C por 7 días; se reemplazó el medio por otro similar y almacenó a -20°C. Se concentró el antígeno y se dosó proteínas. Para la técnica de ELISA se utilizó sueros de pacientes con toxocariasis y de niños recién nacidos, como controles positivos y negativos, respectivamente, diluidos desde ¼ hasta 1/1024. Se sensibilizó placas de poliestireno con varias concentraciones de antígeno, utilizándose conjugado de peroxidasa e IgG de carnero anti IgG humana y sustrato OPD. Se realizó lectura de absorbancia a 492 nm con espectrofotómetro (Multiskan plus labsystems), siendo el punto de corte el promedio aritmético de la absorbancia de los sueros negativos más 3 desviaciones estándar. RESULTADOS: La concentración óptima del antígeno fue 50 ug/mL, la dilución del suero 1/128, la dilución del conjugado 1/1000 con densidad óptica mayor a 0,241. CONCLUSIONES: La técnica de ELISA para diagnóstico serológico de infección humana por Toxocara canis podría ser utilizada en estudios epidemiológicos en nuestro país. Queda pendiente la evaluación de su eficacia en futuros estudios. Palabras clave: Toxocara canis; toxocariasis; serología; ELISA. ELISA TECHNIQUE STANDARDISATION FOR HUMAN TOXOCARIASIS DIAGNOSIS SUMMARYOBJECTIVE: To standardise ELISA technique for Toxocara canis human infection diagnosis by using excreted-secreted antigen prepared in our country. MATERIAL AND METHODS: T. canis eggs were collected by incubation with formalin (2%) at 28 o C in order to obtain third stage larvae that were freed and incubated in RPMI at 37°C for 7 days; the medium was replaced by a similar one and stored at -20°C. Antigen was concentrated and protein dosage was made. Sera from patients with toxocariasis and newborns were used as positive and negative controls by ELISA technique, dilutions ¼ to 1/1024. Polystyrene plates were sensitised with antigen in several concentrations and conjugated peroxidase with horseradish IgG, anti human IgG and substrate OPD were used. Absorbance was read with spectrophotometer (Multiskan plus labsystems) at 492 nm. Cut off point was determined by negative sera absorbencies arithmetic mean plus 3 standard deviations. RESULTS: Antigen concentration was 50 ug/mL, sera dilution 1/128, conjugate dilution 1/1000 with optical density above 0,241. CONCLUSIONS: ELISA technique for serologic diagnosis of human infection by Toxocara canis could be used in epidemiological studies in our country. Its efficacy will be determined in future studies.