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1.
Rev. peru. med. exp. salud publica ; 35(4): 689-694, oct.-dic. 2018. graf
Article in Spanish | LILACS | ID: biblio-985777

ABSTRACT

RESUMEN La hidatidosis es una zoonosis causada por el parásito Echinococcus granulosus. Perú es una zona endémica para esta infección, presentamos el caso de una mujer de 33 años, procedente de la región de Ica; que durante la gestación se le diagnosticó hidatidosis hepática y pulmonar y posterior al término de la gestación fue referida con tubo de drenaje torácico, disnea y dolor torácico en hemitórax derecho, de curso progresivo e imagen tomográfica de tórax que mostró quiste pulmonar basal posterior derecho. Los exámenes serológicos fueron positivos, la paciente fue sometida a resección quirúrgica con resultado histopatológico de quiste hidatídico pulmonar complicado no viable y estructura micótica consistente con aspergiloma. La coexistencia de estas dos entidades es rara y pueden ser amenazas potenciales para los pacientes. El diagnóstico y tratamiento tempranos son vitales para prevenir posibles complicaciones como la hemoptisis masiva o incluso enfermedad invasiva.


ABSTRACT Hydatidosis is a zoonosis caused by the parasite Echinococcus granulosus and Peru is an endemic zone for this infection. We present the case of a 33-year old woman from the region of Ica who, during gestation, was diagnosed with liver and pulmonary hydatidosis. After gestation was terminated, she was referred with thoracic drainage tube, dyspnea, and thoracic pain in right hemithorax, with progressive course and tomographic image of thorax showing right posterior basal pulmonary cyst. The serological analysis was positive, the patient underwent surgical resection with histopathologic result as complex non-viable pulmonary hydatidic cyst and mycotic structure consistent with aspergilloma. The coexistence of these two diseases is rare and can mean potential threats for patients. The early diagnosis and treatment are vital to prevent possible complications such as massive hemoptysis or even invasive disease.


Subject(s)
Adult , Animals , Female , Humans , Pregnancy , Pregnancy Complications, Infectious/parasitology , Echinococcosis, Pulmonary/complications , Pulmonary Aspergillosis/complications , Echinococcosis, Pulmonary/diagnosis , Echinococcosis, Pulmonary/drug therapy , Pulmonary Aspergillosis/diagnosis , Pulmonary Aspergillosis/drug therapy
2.
Rev. chil. infectol ; 33(2): 191-216, abr. 2016. ilus, tab
Article in Spanish | LILACS | ID: lil-784870

ABSTRACT

There is a lot of bacterial, viral or parasite infections who are able to be transmitted vertically from the mother to the fetus or newborn which implicates an enormous risk for it. The TORCH acronym is used universally to refer to a fetus or newborn which presents clinical features compatible with a vertically acquired infection and allows a rational diagnostic and therapeutic approach. The traditional "TORCH test" is nowadays considered not appropriate and it has been replaced for specific test for specific pathogens under well defined circumstances. The present document reviews the general characteristics, epidemiology, pathogenesis, diagnostic and therapeutic options for the most frequently involved pathogens in the fetus or newborn with TORCH suspicion.


Existen numerosas infecciones bacterianas, virales y parasitarias que pueden transmitirse desde la madre al feto o recién nacido (RN) y que significan un riesgo para él. El acrónimo TORCH se utiliza en forma universal para caracterizar a aquel feto o RN que presenta un cuadro clínico compatible con una infección congénita y que permite un enfrentamiento racional, tanto diagnóstico como terapéutico. El concepto tradicional de realizar un "test de TORCH" sin consideraciones específicas a cada paciente, hoy en día se considera no adecuado y ha sido reemplazado por exámenes específicos para patógenos específicos bajo circunstancias bien definidas. El presente documento revisa las características generales, epidemiológicas, patogénicas, diagnósticas y terapéuticas de los patógenos más frecuentemente involucrados en el estudio de pacientes con sospecha de TORCH.


Subject(s)
Humans , Male , Female , Pregnancy , Infant, Newborn , Infant, Newborn, Diseases/microbiology , Infant, Newborn, Diseases/parasitology , Infant, Newborn, Diseases/virology , Pregnancy Complications, Infectious/microbiology , Pregnancy Complications, Infectious/parasitology , Pregnancy Complications, Infectious/virology , Prenatal Diagnosis , Rubella/congenital , Rubella/diagnosis , Rubella/therapy , Syndrome , Toxoplasmosis, Congenital/diagnosis , Toxoplasmosis, Congenital/therapy , Risk Factors , Chagas Disease/congenital , Chagas Disease/diagnosis , Chagas Disease/therapy , Practice Guidelines as Topic , Cytomegalovirus Infections/congenital , Cytomegalovirus Infections/diagnosis , Cytomegalovirus Infections/therapy , Fetus , Herpes Simplex/congenital , Herpes Simplex/diagnosis , Herpes Simplex/therapy
3.
Biomédica (Bogotá) ; 34(4): 631-641, oct.-dic. 2014. ilus, mapas, tab
Article in Spanish | LILACS | ID: lil-730947

ABSTRACT

Durante la última década se han reportado numerosos casos de infección por Trypanosoma cruzi por vía oral, debidos a la contaminación de alimentos con heces de triatominos silvestres o con secreciones de reservorios en áreas donde los vectores domiciliados han sido controlados o no hay antecedentes de domiciliación. Con base en criterios epidemiológicos, clínicos y socioeconómicos, la Organización de las Naciones Unidas para la Agricultura y la Alimentación (FAO) y la Organización Mundial de la Salud (OMS) establecieron una clasificación de los parásitos transmitidos por contaminación de alimentos en diferentes regiones del mundo, en la cual T. cruzi ocupó el décimo lugar de importancia en un grupo de 24 parásitos. Los cambios ambientales, como la deforestación y el calentamiento global, han afectado los ecotopos y el comportamiento de los vectores y de los reservorios de T. cruzi , de manera que estos se han desplazado a nuevas zonas, generando una nueva forma de transmisión por contaminación de alimentos que requiere su evaluación en el país. La presente revisión aborda la transmisión oral de la enfermedad de Chagas con énfasis en los estudios orientados a identificar los factores de riesgo, las especies de triatominos involucrados, la fisiopatología de la infección oral y los genotipos del parásito que están implicados en esta forma de transmisión en Colombia y en otras regiones de América Latina, así como la necesidad de adoptar políticas para su control y vigilancia epidemiológica.


Many cases of infection caused by the oral transmission of Trypanosoma cruzi have been reported during the last decade. These have been due to the contamination of food by faeces from sylvatic triatomines or by leakage from reservoirs in areas where domiciliated vectors have been controlled or where there has been no prior background of domiciliation. The United Nations Food and Agriculture Organization (FAO) and the World Health Organization (WHO) have used epidemiological, clinical and socioeconomic criteria for ranking parasites transmitted by the contamination of food in different areas of the world; T. cruzi was placed tenth in importance amongst a group of 24 parasites in such ranking. Environmental changes such as deforestation and global warming have affected ecotopes and the behaviour of T. cruzi vectors and reservoirs so that these have become displaced to new areas, thereby leading to such new transmission scenario caused by the contamination of food, which requires evaluation in Colombia. The current review deals with the oral transmission of Chagas´ disease, emphasising studies aimed at identifying the pertinent risk factors, the triatomine species involved, the physiopathology of oral infection, the parasite´s genotypes implicated in this type of transmission in Colombia and other Latin American regions, as well as the need for ongoing epidemiological surveillance and control policies.


Subject(s)
Animals , Female , Humans , Pregnancy , Chagas Disease/transmission , Food Parasitology , Feces/parasitology , Fruit/parasitology , Insect Vectors/parasitology , Meat/parasitology , Rhodnius/parasitology , Trypanosoma cruzi/isolation & purification , Vegetables/parasitology , Animals, Wild/parasitology , Armadillos/parasitology , Blood Donors , Beverages/parasitology , Blood Transfusion/adverse effects , Colombia , Chagas Disease/congenital , Chagas Disease/epidemiology , Chagas Disease/parasitology , Disease Reservoirs/parasitology , Genotype , Gastric Mucosa/parasitology , Housing , Mouth Mucosa/parasitology , Parasitemia/parasitology , Parasitemia/transmission , Peptide Hydrolases/physiology , Pregnancy Complications, Infectious/parasitology , Protozoan Proteins/chemistry , Protozoan Proteins/physiology , Risk Factors , Trypanosoma cruzi/genetics , Trypanosoma cruzi/pathogenicity , Trypanosoma cruzi/physiology , Variant Surface Glycoproteins, Trypanosoma/chemistry , Variant Surface Glycoproteins, Trypanosoma/physiology
4.
Biomédica (Bogotá) ; 32(4): 519-526, oct.-dic. 2012. tab
Article in Spanish | LILACS | ID: lil-669099

ABSTRACT

Introducción. El termino ToRCH comprende a los patógenos Toxoplasma gondii, virus de la rubéola, citomegalovirus y virus herpes simple 1 y 2. En mujeres embarazadas expuestas pueden ser causa de abortos y malformaciones congénitas en el neonato. Objetivo. Determinar la seroprevalencia de infección por los agentes causantes del síndrome ToRCH en mujeres en edad fértil de algunas comunidades indígenas yukpa de Venezuela. Materiales y métodos. En el año 2007 fueron seleccionadas 109 muestras de 151 mujeres, en edades comprendidas entre 14 y 40 años. La detección de anticuerpos se hizo por el método de inmunoensayo enzimático indirecto o ELISA de Smartest Diagnostics™. Resultados. El 85,5 % presentó anticuerpos contra T. gondii, el 95,4 % para rubéola, el 75,2 % para citomegalovirus y el 97,2 % para el virus herpes simple 1 y 2. Se observa que el 21,1 % y el 30,2 % presentaron relación entre la variable aborto y las infecciones por citomegalovirus y virus herpes simple 1 y 2, respectivamente. Conclusiones. Existe alta seroprevalencia de infecciones por los agentes causantes del síndrome ToRCH en mujeres en edad fértil de la etnia indígena yukpa. Las condiciones sanitarias precarias y el consumo de agua contaminada con ooquistes, favorecen la adquisición de la infección por T. gondii. El hacinamiento, el inicio a temprana de edad de la actividad sexual y el número de parejas, pueden incidir en la presencia de citomegalovirus y virus herpes simple 1 y 2.


Introduction. The ToRCH syndrome includes the following infectious pathogens: Toxoplasma gondii, rubella, cytomegalovirus and herpes simplex virus 1 and 2. In susceptible pregnant women, these pathogens can cause abortions and congenital malformation in the newborn babies. Objective. The seroprevalence of infection by ToRCH agents was determined in women of childbearing age in several Venezuelan Yukpa indigenous communities. Material and methods. In 2007, 109 samples were selected from 151 women with an age range of 14 to 40 years old. The determination of antibodies against ToRCH agents was carried out through the indirect enzyme immunoassay technique by ELISA´s technique of Smartest Diagnostics. Results. Of the 109 samples, 85.5% presented antibodies against T. gondii, 95.4% for rubella, 75.2% for cytomegalovirus and 97.2% for and herpes simplex virus 1 and 2. A relationship between abortion and infection by cytomegalovirus and herpes simplex virus 1and 2 was noted in 21.1% and 30.2% of women presented, respectively. Conclusions. The findings show a high prevalence of ToRCH agents in women in childbearing age in Yukpa indigenous communities in Venezuela. Poor sanitary conditions and consumption of water contaminated with oocysts may be an important way of transmission of T. gondii. Overcrowding in the communities, sexual activity at an early age and number of partners and may be related to the presence of cytomegalovirus and herpes simplex virus HSV-1 and 2.


Subject(s)
Adolescent , Adult , Female , Humans , Pregnancy , Young Adult , Antibodies, Protozoan/blood , Antibodies, Viral/blood , Cytomegalovirus Infections/epidemiology , Ethnicity/statistics & numerical data , Herpes Simplex/epidemiology , Indians, South American/statistics & numerical data , Measles/epidemiology , Toxoplasmosis/epidemiology , Abortion, Spontaneous/epidemiology , Abortion, Spontaneous/parasitology , Abortion, Spontaneous/virology , Cultural Characteristics , Cytomegalovirus Infections/blood , Cytomegalovirus/immunology , Herpes Simplex/blood , Herpes Simplex/virology , Herpesvirus 1, Human/immunology , /immunology , Measles virus/immunology , Measles/blood , Parity , Prevalence , Pregnancy Complications, Infectious/epidemiology , Pregnancy Complications, Infectious/parasitology , Pregnancy Complications, Infectious/virology , Seroepidemiologic Studies , Toxoplasma/immunology , Toxoplasmosis/blood , Venezuela/epidemiology
5.
Biomédica (Bogotá) ; 32(4): 527-535, oct.-dic. 2012. mapas, tab
Article in Spanish | LILACS | ID: lil-669100

ABSTRACT

Introducción. La determinación de la eficacia de la cloroquina contra Plasmodium vivax permite mejorar la capacidad de vigilancia de la resistencia a los antipalúdicos. Objetivo. Evaluar la eficacia terapéutica de la cloroquina como tratamiento de malaria no complicadapor P. vivax en Riberalta, Guayaramerín y Yacuiba, Bolivia. Materiales y métodos. Se llevó a cabo un estudio de la eficacia in vivo en pacientes mayores de cinco años; se suministró cloroquina (25 mg/kg en tres días) y se hizo seguimiento por 28 días, midiendo los niveles de cloroquina en sangre y desetilcloroquina, el día dos y el día de registro de reaparición de parasitemia. Para la evaluación de la incidencia acumulada de falla del tratamiento, se usó el análisis de supervivencia de Kaplan-Meier. Resultados. Se estudiaron 223 pacientes (Riberalta, 84; Guayaramerín, 80; Yacuiba, 59). Las medias de densidad parasitaria (formas asexuadas) del día 0 en Riberalta fueron de 6.147, en Guayaramerín, 4.251, y en Yacuiba, 5.214 parásitos/μl de sangre. En el mismo orden, los promedios de concentraciones sanguíneas de cloroquina-desetilcloroquina del día 2 fueron de 783, 817 y 815 ng/ml. Mientras en Yacuiba no se presentaron fracasos terapéuticos, en Riberalta ocurrieron con frecuencia de 6,2 % y en Guayaramerín de 10 %. Los valores de cloroquina y desetilcloroquina en sangre de pacientes con fracaso terapéutico fueron menores de 70 ng/ml en el día de reaparición de parasitemia. Conclusión. No se evidenció resistencia de P. vivax a la cloroquina en las tres regiones de evaluación en Bolivia. Se requieren mayores estudios de la concentración de la cloroquina en sangre.


Introduction. Knowledge of the therapeutic efficacy of chloroquine for Plasmodium vivax infections improves the capacity for surveillance of anti-malarial drug resistance. Objective. The therapeutic efficacy of chloroquine as treatment was evaluated for uncomplicated Plasmodium vivax malaria in Bolivia. Materials and methods. An in vivo efficacy study of chloroquine was undertaken in three regions of Bolivia--Riberalta, Guayaramerín and Yacuiba. Two hundred and twenty-three patients (84, 80, and 59 in the three regions, respectively) aged over 5 years old were administered with chloroquine (25 mg/kg/three days) and followed for 28 days. Blood levels of chloroquine and desethylchloroquine were measured on day 2 and on the day of reappearance of parasitemia. The cumulative incidence of treatment failure was calculated using the Kaplan and Meier survival analysis. Results. The mean parasitemias (asexual) on day 0 were 6,147 parasites/μl of blood in the Riberalta population, 4,251 in Guayaramerín and 5,214 in Yacuiba. The average blood concentrations of chloroquine-desethylchloroquine during day 2 were 783, 817, and 815 ng/ml, respectively. No treatment failures were observed in Yacuiba, whereas in Riberalta and Guayaramerín, the frequencies of treatment failures were 6.2% and 10%. Blood levels of chloroquine and desethylchloroquine in patients with treatment failure showed values below 70 ng/ml on the day of reappearance of parasitemia. Conclusion. Resistance of Plasmodium vivax to chloroquine was not demonstrated in three regions of Bolivia.


Subject(s)
Adolescent , Adult , Animals , Child , Child, Preschool , Female , Humans , Male , Middle Aged , Pregnancy , Young Adult , Antimalarials/therapeutic use , Chloroquine/therapeutic use , Malaria, Vivax/drug therapy , Parasitemia/drug therapy , Plasmodium vivax/drug effects , Antimalarials/blood , Bolivia/epidemiology , Chloroquine/analogs & derivatives , Chloroquine/blood , Drug Resistance , Malaria, Vivax/epidemiology , Malaria, Vivax/parasitology , Parasite Load , Parasitemia/epidemiology , Parasitemia/parasitology , Pregnancy Complications, Infectious/drug therapy , Pregnancy Complications, Infectious/epidemiology , Pregnancy Complications, Infectious/parasitology , Rural Population
6.
Braz. j. infect. dis ; 16(2): 170-1174, May-Apr. 2012. ilus, tab
Article in English | LILACS | ID: lil-622739

ABSTRACT

OBJECTIVE: Compare the anti-T. gondii IgG titer between HIV-1 infected and non HIV-1 infected pregnant women and report three cases of congenital toxoplasmosis resulting from reactivation of infection during pregnancy of HIV-1 infected women. METHODS: This study was conducted among 2,270 pregnant women with chronic Toxoplasma gondii infection (absence of IgM and presence of IgG), including 82 HIV-1 infected and 2,188 non-infected women. RESULTS: The average anti-T. gondii IgG titer was 127 for the 2,188 non-HIV-1 infected women, and 227 for the 82 HIV-1-infected women (p = 0,007). These results suggested that higher anti-T. gondii IgG titers in HIV-1-infected pregnant women may not be indicative of an elevated risk for fetal infection. In this study three cases of congenital toxoplasmosis that resulted from infection reactivation during pregnancy of HIV-1-infected women were manifested by fetal death, symptomatic infection, and infant without symptoms, respectively. In two of these women, a ten-fold increase in IgG levels above used cutoff was observed (2,320 UI/mL and 3,613 UI/mL, respectively). In the third pregnant women anti-T. gondii IgG titers during pregnancy did not rise despite the occurrence of congenital toxoplasmosis (204; 198; 172 UI/mL). CONCLUSIONS: Congenital toxoplasmosis resulting reactivation of infection during pregnancy in the studied group leads us to believe that it is a public health problem, especially in our population, in which seroprevalence of T. gondii infections is high. These findings also suggest that special attention is necessary during pregnancy, because the serologic diagnosis may not be indicative of toxoplasmosis reactivation.


Subject(s)
Adult , Female , Humans , Infant, Newborn , Pregnancy , Young Adult , AIDS-Related Opportunistic Infections/parasitology , Antibodies, Protozoan/blood , Immunoglobulin G/blood , Pregnancy Complications, Infectious/parasitology , Toxoplasma/immunology , Toxoplasmosis, Congenital/diagnosis , Toxoplasmosis/transmission , AIDS-Related Opportunistic Infections/immunology , Pregnancy Complications, Infectious/immunology , Retrospective Studies , Risk Factors , Toxoplasmosis, Congenital/immunology , Toxoplasmosis/immunology , Viral Load
7.
Rev. salud pública ; 12(2): 317-326, abr. 2010. ilus, graf
Article in Spanish | LILACS | ID: lil-560860

ABSTRACT

La toxoplasmosis es una zoonosis parasitaria de amplia distribución mundial, que infecta una gran proporción de poblaciones humanas y animales, producida por el parásito Toxoplasma gondii, siendo de gran importancia el contagio de mujeres gestantes, puesto que ésta zoonosis causa enfermedades en los fetos a través de infección transplacentaria; tradicionalmente se ha utilizado una tasa de infección madre-feto constante; sin embargo, hay evidencias de una fuerte relación con la semana de gestación de la madre en el momento de contagiar al feto. Este trabajo describe la dinámica de transmisión de la toxoplasmosis congénita a través de un modelo estructurado en la edad que tiene en cuenta la semana de gestación de la madre; el modelo está acoplado con un modelo espacio-temporal que describe la dispersión de T. gondii a través de gatos, el cual proporciona la cantidad de parásitos en el ambiente, de la cual depende que una mujer gestante se infecte. Se hacen simulaciones variando la cantidad de parásitos y la distancia a la que se encuentra la gestante del lugar del inóculo; además, se varían algunos parámetros equivalentes a posibles medidas de control. Se encuentran cambios importantes al comparar el comportamiento de las poblaciones de gestantes infectadas, cuando se usa tasa de infección madrefeto constante y cuando se usa tasa dependiente de la semana de gestación, lo que permite concluir que la semana de gestación en la que se encuentra la población de gestantes infectadas es fundamental en la transmisión de la infección al feto.


Toxoplasmosis is a parasitic zoonosis having worldwide distribution; it infects many human and animal populations and is produced by the parasite Toxoplasma gondii, this being of great importance in contagion of pregnant women since this zoonosis causes illness in the fetus through transplacental infection. A constant mother-foetus infection rate has traditionally been used. Nevertheless, there is evidence of a strong relationship between a mother's gestation week and the moment when a foetus becomes infected. This work describes congenital toxoplasmosis transmission dynamics by using an age-structured model taking a mother's gestational week into account. The model was adapted to a space-time model describing T. gondii dispersion through cats; this provided the amount of parasites in the environment depending on which a pregnant woman would become infected. Simulations were done, varying the amount of parasites and the pregnant mother-inoculum distance. Some parameters related to possible control measures were also varied. Important changes were found when comparing infected pregnant female population patterns, when a constant mother-fetus infection rate was used and when a dependent pregnancy week rate was used. This led to concluding that the gestation week in which the mothers became infected is fundamental in infection being transmitted to their fetuses.


Subject(s)
Adult , Animals , Cats , Female , Humans , Infant, Newborn , Pregnancy , Computer Simulation , Infectious Disease Transmission, Vertical , Models, Theoretical , Toxoplasmosis, Congenital/transmission , Algorithms , Cat Diseases/transmission , Environmental Exposure , Gestational Age , Pregnancy Complications, Infectious/epidemiology , Pregnancy Complications, Infectious/parasitology , Prenatal Exposure Delayed Effects , Toxoplasmosis, Animal/transmission , Toxoplasmosis, Congenital/epidemiology , Toxoplasmosis, Congenital/parasitology , Toxoplasmosis/epidemiology , Toxoplasmosis/parasitology , Zoonoses
8.
Braz. j. infect. dis ; 11(5): 496-506, Oct. 2007. ilus, tab
Article in English | LILACS | ID: lil-465775

ABSTRACT

Toxoplasmosis is caused by an intracellular protozoan, Toxoplasma gondii, which has a wide geographical distribution. The main infection routes are ingestion of cysts from raw or badly-cooked meat, ingestion of oocysts from substrates contaminated with the feces of infected felines and congenital transmission by tachyzoites. The congenital form results in a severe systemic disease, because if the mother is infected for the first time during gestation, she can present a temporary parasitemia that will infect the fetus. Many of the clinical symptoms are seen in congenitally-infected children, from a mild disease to serious signs, such as mental retardation. Early diagnosis during the pregnancy is highly desirable, allowing prompt intervention in cases of infection, through treatment of pregnant women, reducing the probability of fetal infection and consequent substantial damage to the fetus. Conventional tests for establishment of a fetal diagnosis of toxoplasmosis include options from serology to PCR. Prevention of human toxoplasmosis is based on care to avoid infection, understanding the disease and serological exams during gestation. Pregnant women should be tested serologically from three months gestation, until one month after childbirth. Inclusion of serology for congenital toxoplasmosis along with the basic Guthrie test for PKU is of fundamental importance for early diagnosis of infection and so that treatment is initiated, in order to avoid possible sequels in the infant.


Subject(s)
Female , Humans , Infant, Newborn , Pregnancy , Pregnancy Complications, Infectious/parasitology , Toxoplasmosis, Congenital/prevention & control , Pregnancy Complications, Infectious/diagnosis , Pregnancy Complications, Infectious/therapy , Risk Factors , Toxoplasmosis, Congenital/diagnosis , Toxoplasmosis, Congenital/epidemiology , Toxoplasmosis/diagnosis , Toxoplasmosis/therapy
9.
Rev. argent. microbiol ; 37(4): 217-228, oct.-dic. 2005. ilus, tab
Article in Spanish | LILACS | ID: lil-634509

ABSTRACT

Neospora caninum es agente causal de aborto en bovinos de regiones ganaderas de todo el mundo. Su ciclo de vida es heteroxeno siendo el perro (Canis familiaris) y el coyote (Canis latrans) los hospedadores definitivos reconocidos hasta el presente. La infección transplacentaria es un eficiente mecanismo de transmisión de la enfermedad pero existe evidencia que demuestra la transmisión postnatal en los bovinos. Debido a las pérdidas económicas que causa la neosporosis, diversas técnicas diagnósticas han sido desarrolladas. La fisiopatología del aborto causado por N. caninum no ha sido completamente esclarecida. La modulación del sistema inmune por efecto de la preñez ocasiona un período de susceptibilidad al aborto por N. caninum. Aunque la resistencia al parásito ha sido asociada con una respuesta de linfocitos T tipo 1, dicha respuesta inmune es incompatible con una preñez exitosa. Sin embargo, los mecanismos inmunes presentes en animales crónicamente infectados protegen del aborto ante una segunda exposición al protozoo. La comprensión de esa respuesta inmune adquirida constituye un desafío para el desarrollo de inmunógenos. Este trabajo menciona conceptos generales de la neosporosis bovina haciendo énfasis en los mecanismos inmunes y las perspectivas para la vacunación.


Neospora caninum causes abortions in cattle worldwide. The Neospora-cycle of life is heteroxenous. Dogs (Canis familiaris) and coyotes (Canis latrans) are the definitive hosts known at present. Although, transplacental infection is an efficiently mode of transmission in cattle; there are also experimental and field data that prove horizontal transmission. Several techniques are available for diagnosis since neosporosis is recognized as a disease that causes economic losses in cattle. The mechanisms that produce the abortion are not completely understood. The immunomodulation observed during the pregnancy, is associated with a susceptible period where Neospora-abortion can occur. Resistance to the parasite is dependent on T helper cell 1 cytokine responses. This has important repercussions for pregnant female bovine because strong T helper cell 1 cytokine responses are incompatible with successful pregnancy. However, it was demonstrated that chronically infected cows develop immune mechanisms against the abortion caused by a second Neospora-exposure. The comprehension of those mechanisms is needed for the formulation of Neospora-vaccines that prevent bovine neosporosis. General concepts about neosporosis with emphasis in the immune response and perspectives for vaccination are mentioned in the present review.


Subject(s)
Animals , Cattle , Dogs , Female , Pregnancy , Abortion, Veterinary/etiology , Cattle Diseases/parasitology , Coccidiosis/veterinary , Neospora , Pregnancy Complications, Infectious/veterinary , Abortion, Veterinary/epidemiology , Abortion, Veterinary/immunology , Abortion, Veterinary/parasitology , Abortion, Veterinary/prevention & control , Antibodies, Protozoan/immunology , Argentina/epidemiology , Coccidiostats , Cattle Diseases/diagnosis , Cattle Diseases/epidemiology , Cattle Diseases/immunology , Cattle Diseases/prevention & control , Coccidiosis/diagnosis , Coccidiosis/epidemiology , Coccidiosis/immunology , Coccidiosis/parasitology , Coccidiosis/prevention & control , Dog Diseases/parasitology , Dog Diseases/transmission , Immunity, Cellular , Life Cycle Stages , Neospora/growth & development , Neospora/immunology , Neospora/isolation & purification , Pregnancy Complications, Infectious/epidemiology , Pregnancy Complications, Infectious/parasitology , Pregnancy Complications, Infectious/prevention & control , Protozoan Vaccines/immunology , Th1 Cells/immunology , Vaccination/veterinary
10.
Braz. j. infect. dis ; 6(4): 201-205, aug. 2002.
Article in English | LILACS | ID: lil-331030

ABSTRACT

This report describes a case of Toxoplasma encephalitis during pregnancy of an HIV infected woman who was severely immunosuppressed (CD(4): 17 cells/mm3), had a high viral load (RNA PCR:230,000 copies/ml), was treated with sulfadiazine, pyrimethamine and folinic acid for toxoplasmosis and was being treated with highly potent antiretroviral drugs (AZT, 3TC and nelfinavir) for HIV infection. The newborn was born through an elective C-section, received six weeks of AZT according to the 076 protocol and was clinically normal at birth. Subsequently he had two RNA PCR negatives for HIV, seroreverted and had no clinical or laboratory evidence of congenital toxoplasmosis. Despite the concerns of the use of these combined therapies on the foetus during pregnancy, their efficacy illustrates that keeping the mother alive and in good health is an important strategy to protect the unborn child from acquiring these two infections.


Subject(s)
Adult , Animals , Female , Humans , Infant, Newborn , Pregnancy , AIDS-Related Opportunistic Infections/drug therapy , AIDS-Related Opportunistic Infections/parasitology , HIV Infections/complications , HIV Infections/transmission , Infectious Disease Transmission, Vertical , Toxoplasmosis, Cerebral , Anti-HIV Agents , Antiretroviral Therapy, Highly Active , Pregnancy Complications, Infectious/drug therapy , Pregnancy Complications, Infectious/parasitology , Pregnancy Complications, Infectious/virology , Infant, Newborn, Diseases/drug therapy , Infant, Newborn, Diseases/parasitology , Infant, Newborn, Diseases/virology , HIV , AIDS-Related Opportunistic Infections/transmission , HIV Infections/drug therapy , HIV Infections/virology , Infectious Disease Transmission, Vertical , Toxoplasma , Toxoplasmosis, Cerebral , Treatment Outcome , Viral Load
11.
Rev. Soc. Bras. Med. Trop ; 22(2): 99-101, abr.-jun. 1989.
Article in Portuguese | LILACS | ID: lil-92355

ABSTRACT

Em 1982 e em 1985 foram observados em Humaitá, Estado do Amazonas, respectivamente, uma criança lactente e uma gestante tercigesta, no segundo trimestre da gravidez, ambas com malária pelo Plamodium falciparum. O lactente, masculino, natural do Amazonas tinha um mês de idade e apresentava malária desde o décimo dia após o nascimento. Sua mäe tinha 19 anos, era natural do Amazonas e apresentara a primo-infecçäo palustre no dia do parto, desse que era o seu segundo filho. O outro caso era o de uma gestante com 22 anos, natural do Amazonas, que tinha 2 filhos, um de 8 e outro de 6 anos e apresentara três surtos prévios de malária, o primeiro em 1983 e o último em março de 1985. Quando foi atendida estava com malária e no 2§ trimestre do gestaçäo. Tanto o lactente, quanto a gestante foram tratados com clindamicina e tiveram cura clínica e parasitária. O lactente provavelmente apresentou malária congênita, ou intraparto, pelo curto período de incubaçäo, que apresentou. Ao contrário do que tem sido descrito em áreas hiperendêmicas a gestante apresentou malária na terceira gestaçäo, embora tenha se comportado como primigesta, do ponto de vista da imunidade, pois os surtos prévios que teve ocorreram após as gestaçöes anteriores


Subject(s)
Humans , Pregnancy , Infant, Newborn , Adult , Animals , Male , Female , Malaria/parasitology , Pregnancy Complications, Infectious/parasitology , Malaria/drug therapy , Malaria/transmission , Plasmodium falciparum , Pregnancy Complications, Infectious/drug therapy
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