RESUMO
Toxoplasma gondii (T gondii) infection has been associated with protection against allergy and autoimmune diseases. We investigated the effects of T gondii infection on cytokine and antibody responses in atopic and nonatopic Brazilian subjects. We have measured in whole-blood cultures, Th1 (IFN-γ and IL-12), Th2 (IL-5) and regulatory cytokine IL-10 in blood cells unstimulated and stimulated with pokeweed mitogen or T gondii soluble tachyzoites antigen (STAg) or Dermatophagoides pteronyssinus antigen. A significant negative association was found between high levels of anti-dust mite IgE and T gondii seropositivity (OR = 0.46; 95%CI = 0.25-0.85). STAg stimulation induced a mixed profile of Th1 and Th2 cytokines (IFN-γ, IL-12 and IL-5) in Tg-positive atopic individuals compared with Tg-negative atopic individuals (P < .0001, P = .033 and P = .003, respectively). In contrast, IL-10 production was not different between these groups. No association was found between T gondii infection and asthma. We hypothesized that the protective effect on atopy might be related to the strong Th1 immune response to T gondii found on the seropositive subjects. From our knowledge, this is the first study to investigate the association between atopy and T gondii infection in Brazilian subjects, analysing the cellular immune responses.
Assuntos
Anticorpos Antiprotozoários/análise , Hipersensibilidade/imunologia , Imunidade Celular , Imunoglobulina E/imunologia , Toxoplasmose/imunologia , Adulto , Animais , Antígenos de Protozoários/imunologia , Asma/imunologia , Brasil , Citocinas/análise , Feminino , Humanos , Imunoglobulina G/sangue , Interleucina-10/imunologia , Pessoa de Meia-Idade , Pyroglyphidae/imunologia , Toxoplasma/imunologiaRESUMO
This work reports results of re-infection of BALB/c and C57BL/6 mice with different recombinant strains of Toxoplasma gondii. Mice were prime-infected with the non-virulent D8 strain and challenged with virulent strains. PCR-RFLP of cS10-A6 genetic marker of T. gondii demonstrated that BALB/c mice were re-infected with the EGS strain, while C57BL/6 mice were re-infected with the EGS and CH3 strains. Levels of IFN-γ and IL-10 after D8 prime-infection were lower in C57BL/6 than in BALB/c mice. Brain inflammation after D8 prime-infection was more intense in C57BL/6 than in BALB/c mice. It was shown that re-infection depends on mice lineage and genotype of the strain used in the challenge.
Assuntos
Toxoplasma/imunologia , Toxoplasmose Animal/imunologia , Animais , Bioensaio , Encéfalo/parasitologia , Encéfalo/patologia , Células Cultivadas , Galinhas , Citocinas/análise , Cães , Feminino , Genótipo , Humanos , Camundongos , Camundongos Endogâmicos BALB C , Camundongos Endogâmicos C57BL , Reação em Cadeia da Polimerase , Polimorfismo de Fragmento de Restrição , Recidiva , Baço/citologia , Baço/imunologia , Toxoplasma/classificação , Toxoplasma/genéticaRESUMO
The aim of this study was to evaluate the utility of western blot (WB) analysis as a diagnostic tool for congenital toxoplasmosis in 215 newborn infants. The children were submitted to clinical examinations to assess macular, neurological and hearing signals. The WB results obtained were compared to the persistence of IgG antibodies at the end of 12 months, which is regarded as the "gold standard" diagnosis of congenital toxoplasmosis. Association between the WB results and the clinical signs presented by the infants was also assessed. Of the 215 children, 177 had a confirmed congenital toxoplasmosis diagnosis and 38 were uninfected. IgG-WB showed a sensitivity of 73.5% and a specificity of 97.4%. IgM-WB showed a sensitivity of 54.8% and a specificity of 94.7%. The IgG-WB and IgM-WB combination increased the sensitivity to 86.5%. The IgM-WB-positive children had a 1.4-fold greater risk of presenting active macular lesions than did those that were IgM-WB-negative. This study showed that the WB assay is a useful tool to confirm a diagnosis of congenital toxoplasmosis and that the IgM-WB-positive results can indicate active macular lesions in newborn infants.
Assuntos
Anticorpos Antiprotozoários/sangue , Imunoglobulina G/sangue , Imunoglobulina M/sangue , Toxoplasma/imunologia , Toxoplasmose Congênita/diagnóstico , Western Blotting , Ensaio de Imunoadsorção Enzimática , Sangue Fetal/imunologia , Sangue Fetal/parasitologia , Humanos , Recém-Nascido , Triagem Neonatal , Sensibilidade e EspecificidadeRESUMO
Although several Toxoplasma gondii genotyping studies have been performed in Brazil, studies of isolates from animals in the state of Minas Gerais are rare. The objective of this study was to conduct a genotypic characterization of T. gondii isolates obtained from dogs, free-range chickens, and humans in Minas Gerais and to verify whether the T. gondii genotypes circulating in domestic animals correspond to the genotypes detected in humans. Genetic variability was assessed by restricted fragment length polymorphism at 11 loci (SAG1, 5'+3'SAG2, SAG2 alt, SAG3, BTUB, GRA6, c22-8, c29-2, L358, PK1, and Apico). Twelve different genotypes were identified among the 24 isolates studied, including 8 previously identified genotypes and 4 new genotypes. The genetic relationship of the 24 T. gondii isolates, together with the genotypes previously described from 24 human newborns with congenital toxoplasmosis, revealed a high degree of similarity among the genotypes circulating in humans and animals in Minas Gerais. The most common genotypes among these species were BrII, BrIII, ToxoDB #108, and ToxoDB #206. Restricted fragment length polymorphism at the CS3 locus of these 48 isolates showed that the majority of isolates presented alleles I (50%) or II (27%). Isolates harboring allele III at the CS3 locus presented low virulence for mice, whereas those harboring alleles I or II presented higher virulence. These results confirm the utility of marker CS3 for predicting the virulence of Brazilian isolates of T. gondii in mice. No association was found between the allele type and clinical manifestations of human congenital toxoplasmosis. This is the first report of T. gondii genotyping that verifies the overlapping genotypes of T. gondii from humans and animals in the same geographic region of Brazil. Our results suggest that there is a common source of infection to the species studied, most likely oocysts contaminating the environment.
Assuntos
Genótipo , Toxoplasma/classificação , Toxoplasma/genética , Toxoplasmose Animal/parasitologia , Toxoplasmose/parasitologia , Alelos , Animais , Animais Domésticos , Brasil , DNA de Protozoário/genética , Humanos , Tipagem de Sequências Multilocus , Filogenia , Toxoplasma/patogenicidade , Toxoplasmose/epidemiologia , Toxoplasmose Animal/epidemiologia , Virulência/genéticaRESUMO
Serum samples of 930 sheep were tested by ELISA to assess the prevalence of anti-Toxoplasma gondii antibodies and to identify risk factors associated with the presence of toxoplasmosis in two regions of Rio Grande do Norte (Northeast Brazil), with different climatic conditions. The overall estimated prevalence was 22.1%, with 26.3% and 17.8% positive sheep in Leste Potiguar and Central Potiguar regions, respectively. Among the positive sheep, 18.1% had low-avidity IgG antibodies, suggesting the occurrence of recent toxoplasmosis. The risk factors for toxoplasmosis in sheep were: presence of cats (odds ratio (OR) = 1.55; confidence interval (CI) 95% = 1.11-2.16), age of the animals, with adults presenting a greater chance of infection (OR = 2.44; CI 95% = 1.58-3.75), and the use of running water (OR = 1.61; CI 95% = 1.25-2.09), characterizing the existence of transmission by sporulated oocysts of T. gondii in the environment.
Assuntos
Anticorpos Antiprotozoários/sangue , Doenças dos Ovinos/epidemiologia , Toxoplasma/imunologia , Toxoplasmose Animal/epidemiologia , Fatores Etários , Animais , Afinidade de Anticorpos , Brasil/epidemiologia , Gatos , Intervalos de Confiança , Ensaio de Imunoadsorção Enzimática/veterinária , Feminino , Imunoglobulina G/sangue , Masculino , Razão de Chances , Fatores de Risco , Estudos Soroepidemiológicos , Ovinos , Doenças dos Ovinos/parasitologia , Abastecimento de ÁguaRESUMO
OBJECTIVE: To report a rare case of congenital toxoplasmosis from an immunocompetent mother with chronic infection who had reactivation of ocular disease during pregnancy. DESCRIPTION: The newborn was asymptomatic at birth and identified by neonatal screening (IgM anti-Toxoplasma gondii in dried blood) among other 190 infants with congenital toxoplasmosis during a 7-month period. His mother had had a non-treated episode of reactivation of toxoplasmic retinochoroiditis during pregnancy, with stable IgG titers and negative IgM results. Results of IgM and IgG in the newborn's serum, as well as IgG immunoblotting were positive and active retinochoroidal lesions were detected in his peripheral retina. The neonate was treated with sulfadiazine, pyrimethamine and folinic acid. At 14 months of life, the child remained asymptomatic, with regression of retinochoroidal lesions and persistence of IgG. COMMENTS: It is possible that systematic neonatal screening in areas with high prevalence of infection may identify these cases.
Assuntos
Coriorretinite/parasitologia , Transmissão Vertical de Doenças Infecciosas , Complicações Parasitárias na Gravidez , Toxoplasmose Ocular/transmissão , Coriorretinite/congênito , Coriorretinite/imunologia , Feminino , Humanos , Recém-Nascido , Triagem Neonatal/métodos , Gravidez , Complicações Parasitárias na Gravidez/tratamento farmacológico , Complicações Parasitárias na Gravidez/imunologia , Recidiva , Toxoplasmose Ocular/congênito , Toxoplasmose Ocular/imunologiaRESUMO
O município de Mossoró/RN, no Nordeste do Brasil, tem como destaque a criação de caprinos. A toxoplasmose é uma zoonose que é mais patogênico para os caprinos do que para os demais animais de abate. Em caprinos, o protozoário frequentemente é responsável por problemas reprodutivos e perdas econômicas. Com o objetivo de identificar a soroprevalência e os fatores de risco da toxoplasmose em caprinos de propriedades rurais do Município de Mossoró, amostras de soro de 338 animais (320 fêmeas e 18 machos) de 15 unidades produtoras foram testados pelo Ensaio Imunoenzimático (ELISA). Das 15 propriedades, 14 apresentaram animais soropositivos para toxoplasmose, e nestas o total de animais positivos foram de 125 (123 fêmeas e 2 machos), obtendo uma prevalência de 37,0%. Houve uma relação significativa (p<0,05) entre a prevalência e o sexo, e entre a prevalência e raça dos animais. As chances de ocorrer (OR) mais importantes associados à infecção por Toxoplasma gondii foram: fonte de água (OR=2,635), vasilhames para a água dos animais localizado fora das instalações da propriedade (OR=3,121) e a exploração do tipo leiteira (OR=2,546). Pela análise do ELISA de avidez, foram encontradas fêmeas em idade reprodutiva na fase aguda da infecção.
The municipality of Mossoró, RN, Northeastern Brazil, is featured on goat rearing. Toxoplasmosis is a zoonosis which is more pathogenic for goats when compared with other animals for slaughter. In this species, the protozoan is often responsible for reproductive problems and economic losses. In order to identify the seroprevalence and risk factors of toxoplasmosis in goats of farms in this municipality, serum samples from 338 animals (320 females and 18 males) of 15 production units were tested by enzyme immunoassay (ELISA). Of the 15 farms, 14 had animals positive for Toxoplasma gondii, and in these the total number of seropositive animals were 125 (123 females and 2 males), yielding a prevalence of 37.0%. There was a significant relationship (p<0.05) between prevalence and sex, and between the prevalence and breed of animals. The most important risk factors associated with T. gondii infection were: water supply with odds ratio (OR=2.635), containers for water animals located outside the premises of property (OR=3.121) and the exploitation of dairy type (OR=2.546). For the analysis of the avidity ELISA, was found females of reproductive age in the acute phase of infection.
Assuntos
Animais , Ensaio de Imunoadsorção Enzimática/veterinária , Ovinos/parasitologia , Toxoplasma/isolamento & purificação , Estudos Epidemiológicos , Fatores de RiscoRESUMO
Toxoplasma gondii strains displaying the Type I/III genotype are associated with acquired ocular toxoplasmosis in humans. Here, we used a mice model to characterize some immunological mechanisms involved in host resistance to infection with such strains. We have chosen the Type I/III strains D8, G2 and P-Br, which cause a chronic infection in mice that resembles human toxoplamosis. Mice deficient of molecules MyD88, IFN-gamma, and IL-12 were susceptible to all three parasite strains. This finding indicates the importance of innate mechanisms in controlling infection. On the other hand, MHC haplotype did not influenced resistance/susceptibility; since mice lineages displaying a same genetic background but different MHC haplotypes (H2b or H2d) developed similar mortality and cyst numbers after infection with those strains. In contrast, the C57BL/6 genetic background, and not MHC haplotype, was critical for development of intestinal inflammation caused by any of the studied strains. Finally, regarding effector mechanisms, we observed that B and CD8+ T lymphocytes controlled survival,whereas the inducible nitric oxide synthase influenced cyst numbers in brains of mice infected with Type I/III strains. These findings are relevant to further understanding of the immunologic mechanisms involved in host protection and pathogenesis during infection with T. gondii.
Assuntos
Haplótipos/genética , Complexo Principal de Histocompatibilidade/genética , Camundongos Endogâmicos/imunologia , Toxoplasma/genética , Toxoplasmose Animal/imunologia , Toxoplasmose Cerebral/imunologia , Animais , Modelos Animais de Doenças , Genótipo , Interferon gama/deficiência , Interferon gama/imunologia , Interleucina-12/deficiência , Interleucina-12/imunologia , Complexo Principal de Histocompatibilidade/imunologia , Camundongos , Camundongos Endogâmicos/genética , Fator 88 de Diferenciação Mieloide/deficiência , Fator 88 de Diferenciação Mieloide/imunologia , Fatores de Tempo , Receptores Toll-Like/imunologia , Toxoplasma/patogenicidade , Toxoplasmose Animal/parasitologia , Toxoplasmose Animal/patologia , Toxoplasmose Cerebral/parasitologia , Toxoplasmose Cerebral/patologia , Virulência/genéticaRESUMO
The compound 2-hydroxy-3-(1'-propen-3-phenyl)-1,4-naphthoquinone (PHNQ6) was evaluated for activity against Toxoplasma gondii, alone or combined with sulfadiazine. Treatment with PHNQ6 combined with sulfadiazine protected at least 70 and 90% of mice infected with RH and EGS strains, respectively. Mice were treated with PHNQ6 (50 mg/kg/day) alone or combined with sulfadiazine (40 mg/L) 30 days after infection with P strain. The number of brain cysts was lower in mice treated with PHNQ6 alone or combined with sulfadiazine compared to that in control mice. Degenerated bradyzoites were observed in animals treated with PHNQ6. Infectivity of bradyzoites treated with PHNQ6 alone or combined with sulfadiazine was inhibited after in vitro incubation.
Assuntos
Antiprotozoários/farmacologia , Naftoquinonas/farmacologia , Sulfadiazina/farmacologia , Toxoplasma/efeitos dos fármacos , Toxoplasmose Animal/tratamento farmacológico , Animais , Antiprotozoários/uso terapêutico , Quimioterapia Combinada , Feminino , Camundongos , Naftoquinonas/uso terapêutico , Distribuição Aleatória , Sulfadiazina/uso terapêutico , Resultado do TratamentoRESUMO
Previous studies have shown a high prevalence of toxoplasmosis and the frequent occurrence of ocular disease in Brazil. To identify the genotypes of parasite strains associated with ocular disease, we compared 25 clinical and animal isolates of Toxoplasma gondii from Brazil to previously characterized clonal lineages from North America and Europe. Multilocus nested polymerase chain reaction analysis was combined with direct sequencing of a polymorphic intron to classify strains by phylogenetic methods. The genotypes of T. gondii strains isolated from Brazil were highly divergent when compared to the previously described clonal lineages. Several new predominant genotypes were identified from different regions of Brazil, including 2 small outbreaks attributable to foodborne or waterborne infection. These findings show that the genetic makeup of T. gondii is more complex than previously recognized and suggest that unique or divergent genotypes may contribute to different clinical outcomes of toxoplasmosis in different localities.
Assuntos
Toxoplasma/genética , Toxoplasmose Ocular/parasitologia , Animais , Antígenos de Protozoários/química , Antígenos de Protozoários/genética , Brasil , DNA de Protozoário/química , DNA de Protozoário/genética , Variação Genética , Genótipo , Humanos , Glicoproteínas de Membrana/química , Glicoproteínas de Membrana/genética , Pentosiltransferases/química , Pentosiltransferases/genética , Filogenia , Reação em Cadeia da Polimerase , Polimorfismo de Fragmento de Restrição , Proteínas de Protozoários/química , Proteínas de Protozoários/genética , Toxoplasma/crescimento & desenvolvimento , Toxoplasma/isolamento & purificação , Toxoplasmose Ocular/sangueRESUMO
Objetivo: Apresentar um caso raro de toxoplasmose congênita de uma mãe imunocompetente com infecção crônica que teve reativação da doença ocular durante a gestação. Descrição: O recém-nascido estava assintomático no nascimento e foi identificado através de triagem neonatal (IgM anti-Toxoplasma gondii em sangue seco) entre outros 190 bebês com toxoplasmose congênita durante um período de 7 meses. Sua mãe tinha tido um episódio não tratado de reativação de retinocoroidite toxoplásmica durante a gestação, com títulos de IgG estáveis e resultados negativos para IgM. Os resultados de IgM e IgG no soro do recém-nascido e o teste de immunoblotting para IgG foram positivos, e detectou-se lesões retinocoroideanas ativas na periferia da retina. O recém-nascido foi tratado com sulfadiazina, pirimetamina e ácido folínico. Aos 14 meses de vida, a criança permanecia assintomática, com regressão das lesões retinocoroideanas e persistência de IgG. Comentários: É possível que a triagem neonatal sistemática em áreas com alta prevalência de infecção possa identificar esses casos.
Objectives: To report a rare case of congenital toxoplasmosis from an immunocompetent mother with chronic infection who had reactivation of ocular disease during pregnancy. Descriptions:The newborn was asymptomatic at birth and identified by neonatal screening (IgM anti-Toxoplasma gondii in dried blood) among other 190 infants with congenital toxoplasmosis during a 7-month period. His mother had had a non-treated episode of reactivation of toxoplasmic retinochoroiditis during pregnancy, with stable IgG titers and negative IgM results. Results of IgM and IgG in the newborns serum, as well as IgG immunoblotting were positive and active retinochoroidal lesions were detected in his peripheral retina. The neonate was treated with sulfadiazine, pyrimethamine and folinic acid. At 14 months of life, the child remained asymptomatic, with regression of retinochoroidal lesions and persistence of IgG. Comments: It is possible that systematic neonatal screening in areas with high prevalence of infection may identify these cases.
Assuntos
Feminino , Humanos , Recém-Nascido , Gravidez , Coriorretinite/parasitologia , Transmissão Vertical de Doenças Infecciosas , Complicações Parasitárias na Gravidez , Toxoplasmose Ocular/transmissão , Coriorretinite/congênito , Coriorretinite/imunologia , Triagem Neonatal/métodos , Complicações Parasitárias na Gravidez/tratamento farmacológico , Complicações Parasitárias na Gravidez/imunologia , Recidiva , Toxoplasmose Ocular/congênito , Toxoplasmose Ocular/imunologiaRESUMO
Herein we characterized various genetic markers and the biological behavior of a natural recombinant strain of Toxoplasma gondii (P-Br). From nine genetic markers analyzed, three (B1, ROP1, and SAG1) and three (cS10-A6, GRA6, and SAG3) markers belong to parasites from the type I and type III lineages, respectively. The SAG2 and L363 loci were shown to be type I-III chimera alleles. The cB2l-4 microsatellite marker showed a unique haplotype. The P-Br strain presented low virulence in the acute phase of infection and was cystogenic during the chronic infection. The interleukin 12/gamma interferon axis and inducible nitric oxide synthase were main determinants of resistance during the acute infection with the P-Br strain. As opposed to infection with the type II strain of T. gondii (ME-49), peroral infection with the P-Br strain led only to a light inflammatory infiltrate and no major lesions in the intestine of the C57BL/6 mice. In addition, the BALB/c (resistant to ME-49) and C57BL/6 (susceptible to ME-49) mice were shown, respectively, to be more susceptible and more resistant to cyst formation and toxoplasmic encephalitis when infected with the P-Br strain. Further, the C57BL/KsJ and DBA2/J congenic strains containing major histocompatibility complex (MHC) haplotype "d" were more resistant than the parental strains (C57BL/6 and DBA1/J), when infected with the ME-49 but not with the P-Br strain. Together, our results indicate that resistance to cyst formation and toxoplasmic encephalitis induced during infection with P-Br is not primarily controlled by the MHC haplotype d, as previously reported for type II strains of T. gondii.
Assuntos
Citocinas/fisiologia , Complexo Principal de Histocompatibilidade/fisiologia , Toxoplasmose Animal/imunologia , Animais , Haplótipos , Interferon gama/fisiologia , Interleucina-12/fisiologia , Camundongos , Camundongos Endogâmicos , Óxido Nítrico Sintase/fisiologia , Óxido Nítrico Sintase Tipo II , Recombinação Genética , Toxoplasma/genéticaRESUMO
A cross-sectional household study involving 499 individuals was undertaken in an area of Minas Gerais state, Brazil, where infection with Toxoplasma gondii is endemic. Nearly 50% (n=247) of the sample had T. gondii-specific antibodies, even individuals in the 5-9-year-old age group. Approximately 12.5% (n=28) of a random subsample of participants who were positive for T. gondii antibodies had ocular lesions associated with T. gondii infection. The frequency of ocular toxoplasmosis increased significantly with age, with approximately 50% of individuals >60 years of age having lesions. The size of the ocular lesion correlated positively (r=0.85; P=.01) with the serum level of immunoglobulin A specific for tachyzoite-derived glycoinositolphospholipids. We found that sharing the same residence accounted for 30% of the variation in infectivity among residents in the sample, whereas age was the main risk factor for development of ocular toxoplasmosis in patients who were positive for T. gondii antibodies.
Assuntos
Glicolipídeos/imunologia , Imunoglobulina A/sangue , Fosfolipídeos/imunologia , Índice de Gravidade de Doença , Toxoplasma/imunologia , Toxoplasmose Ocular/epidemiologia , Adolescente , Adulto , Distribuição por Idade , Fatores Etários , Idoso , Idoso de 80 Anos ou mais , Animais , Anticorpos Antiprotozoários/sangue , Especificidade de Anticorpos , Brasil , Criança , Pré-Escolar , Feminino , Humanos , Lactente , Masculino , Pessoa de Meia-Idade , Distribuição por Sexo , Toxoplasmose Ocular/parasitologia , Toxoplasmose Ocular/fisiopatologiaRESUMO
Toxoplasma gondii strains displaying the Type I/III genotype are associated with acquired ocular toxoplasmosis in humans. Here, we used a mice model to characterize some immunological mechanisms involved in host resistance to infection with such strains. We have chosen the Type I/III strains D8, G2 and P-Br, which cause a chronic infection in mice that resembles human toxoplamosis. Mice deficient of molecules MyD88, IFN-gamma, and IL-12 were susceptible to all three parasite strains. This finding indicates the importance of innate mechanisms in controlling infection. On the other hand, MHC haplotype did not influenced resistance/susceptibility; since mice lineages displaying a same genetic background but different MHC haplotypes (H2b or H2d) developed similar mortality and cyst numbers after infection with those strains. In contrast, the C57BL/6 genetic background, and not MHC haplotype, was critical for development of intestinal inflammation caused by any of the studied strains. Finally, regarding effector mechanisms, weobserved that B and CD8+ T lymphocytes controlled survival,whereas the inducible nitric oxide synthase influenced cyst numbers in brains of mice infected with Type I/III strains. These findings are relevant to further understanding of the immunologic mechanisms involved in host protection and pathogenesis during infection with T. gondii.
Cepas de Toxoplasma gondii que apresentam o genótipo I/III são associadas a toxoplasmose ocular adquirida em humanos. No presente trabalho, nós utilizamos um modelo da doença em camundongos para caracterizar mecanismos imunológicos envolvidos na resistência do hospedeiro à infecção por aquelas cepas. Escolhemos as cepas D8, G2 e P-Br, que causam infecção crônica em camundongos, semelhante à toxoplasmose humana. Camundongos deficientes em MyD88, IFN-G e IL-12 foram susceptíveis a infecções com todas as três linhagens do parasita. Esses dados indicam a importância de mecanismos inatos no controle da infecção. Por outro lado, o haplótipo do MHC não influenciou na resistência/susceptibilidade, na medida em que linhagens de camundongos com um mesmo "background'' genético, mas diferentes haplótipos de MHC (H2b e H2d) apresentam o índice de mortalidade e número de cistos semelhantes após a infecção com aquelas cepas do parasita. Em contraste, o "background'' genético de C57BL/6, mas não o haplótipo de MHC, foi crítico para o desenvolvimento de inflamação intestinal causada pelas cepas estudadas. Finalmente, com relação aos mecanismos efetores, observamos que linfócitos B e T CD8+ controlam a sobrevivência após infecção. Por outro lado, a ativação da enzima óxido nítrico sintase induzida foi um fator importante para controle do número de cistos cerebrais em camundongos infectados com cepas do Tipo I/III. Esses achados são relevantes para o melhor entendimento dos mecanismos imunológicos envolvidos na proteção e patogênese durante infecção com T. gondii.
Assuntos
Animais , Camundongos , Haplótipos/genética , Complexo Principal de Histocompatibilidade/genética , Camundongos Endogâmicos/imunologia , Toxoplasma/genética , Toxoplasmose Animal/imunologia , Toxoplasmose Cerebral/imunologia , Modelos Animais de Doenças , Genótipo , Interferon gama/deficiência , Interferon gama/imunologia , /deficiência , /imunologia , Complexo Principal de Histocompatibilidade/imunologia , Camundongos Endogâmicos/genética , /deficiência , /imunologia , Fatores de Tempo , Receptores Toll-Like/imunologia , Toxoplasma/patogenicidade , Toxoplasmose Animal/parasitologia , Toxoplasmose Animal/patologia , Toxoplasmose Cerebral/parasitologia , Toxoplasmose Cerebral/patologia , Virulência/genéticaRESUMO
A infeccao experimental pelo Trypanosoma cruzi foi estudada em nove caprinos jovens. Os animais foram inoculados via intraperitoneal com 1000 tripomastigotas sanguineos/Kg de peso com as cepas 147 (Grupo 1) e 229 (Grupo 2), isoladas de pacientes chagasicos cronicos de Babui, MG. Realizaram-se exames de sangue a fresco, xenodiagnostico, hemocultura e sorologia (RIFI e ELISA)...
Assuntos
Animais , Cabras/parasitologia , Reservatórios de Doenças/veterinária , Trypanosoma cruzi/isolamento & purificação , Doença de Chagas/epidemiologia , Trypanosoma cruzi/parasitologiaRESUMO
Different toxoplasma antigens were entrapped within liposomes and evaluated, in this form, for their ability to protect Swiss mice against toxoplasma infection: soluble tachyzoite antigen (L/TAg), tissue cyst (L/CAg), tachyzoite plus tissue cyst (L/TCAg) or purified antigen of tachyzoite (L/pTAg). The protein used in L/pTAg was purified from tachyzoites using a stage-specific monoclonal antibody which reacted at a molecular weight of 32 kD in SDS PAGE and silver stain using reduced condition. To compare the immuno-adjuvant action of liposomes and of Freund's Complete Adjuvant (FCA), another group of mice was immunized with soluble tachyzoite antigen (STAg) emulsified in FCA (FCA/TAg). Control groups were inoculated with (STAg) alone, phosphate-buffered saline (PBS), FCA with PBS (FCA/PBS) and empty liposomes (L/PBS). Mice were inoculated subcutaneously with these antigens six, four and two weeks before a challenge with 80 tissue cysts of the P strain of Toxoplasma gondii orally. All mice immunized with or without adjuvant showed a humoral response, as measured by Elisa. However, no correlation was found between antibody titer and protection against the challenge. All mice immunized with L/pTAg or L/TCAg survived (100), whereas 80 percent and 90 percent of mice from groups which received respectively PBS or FCA/PBS and L/PBS died. All mice immunized with antigens entrapped within liposomes (L/TAg, L/CAg, L/TCAg and L/pTAg) showed low numbers of intracerebral cysts
Assuntos
Animais , Feminino , Camundongos , Antígenos de Protozoários/administração & dosagem , Proteínas de Protozoários/imunologia , Vacinas Protozoárias/imunologia , Toxoplasma/imunologia , Toxoplasmose/prevenção & controle , Anticorpos Monoclonais , Antígenos de Protozoários/isolamento & purificação , Relação Dose-Resposta Imunológica , Portadores de Fármacos , Ensaio de Imunoadsorção Enzimática , Lipossomos , Toxoplasma/isolamento & purificação , Toxoplasmose/imunologiaRESUMO
Distinct Toxoplasma gondii antigens were entrapped within liposomes and evaluated for their ability to protect Balb/c mice against congenital transmission: soluble tachyzoite antigen (L/STAg), soluble tissue cyst antigen (L/SCAg), soluble tachyzoite plus tissue cyst (L/STCAg) or purified 32kDa antigen of tachyzoite (L/pTAg). Soluble tachyzoite antigen alone in PBS (STAg) or emulsified in Freund's Complete Adjuvant (FCA/STAg) was also evaluated. Dams were inoculated subcutaneously with these antigens 6, 4 and 2 weeks prior to a challenge with four tissue cysts of the P strain of T. gondii orally between 10 and 14 days of pregnancy. Significant diminution differences were observed between the frequency of infected pups born of the dams immunized with the antigens incorporated into liposomes and that of pups born of the dams immunized with antigen emulsified in FCA or non immunized group (p<0.05). There was a significant decrease in the number of pups born dead in the groups L/STAg, L/SCAg and L/pTAg when compared with pups from all other groups (p <0.05). All dams immunized with or without adjuvant showed an antibody response and a proliferation of T-cells. However, no correlation was found between immune response and protection against the challenge