RESUMO
Sporotrichosis is a chronic infection caused by the dimorphic fungus Sporothrix schenckii, involving all layers of skin and the subcutaneous tissue. The role of innate immune toll-like receptors 2 and 4 in the defense against this fungus has been reported, but so far, there were no studies on the effect of cell wall major components over the cytosolic oligo-merization domain (NOD)-like receptors, important regulators of inflammation and responsible for the maturation of IL-1ß and IL-18, whose functions are dependents of the caspase-1 activation, that can participate of inflammasome. It was evaluated the percentage of activation of caspase-1, the production of IL-1ß, IL-18, IL-17, IFN-γ and nitric oxide in a Balb/c model of S. schenckii infection. It was observed a decreased activity of caspase-1 during the fourth and sixth weeks of infection accompanied by reduced secretion of the cytokines IL-1ß, IL-18 and IL-17 and high production of nitric oxide. IFN-γ levels were elevated during the entire time course of infection. This temporal reduction in caspase-1 activity coincides exactly with the reported period of fungal burden associated with a transitory immunosuppression induced by this fungus and detected in similar infection models. These results indicate the importance of interaction between caspase-1, cytokines IL-1ß and IL-18 in the host defense against S. schenckii infection, suggesting a participation the inflammasome in this response.
Assuntos
Caspase 1/metabolismo , Interferon gama/biossíntese , Óxido Nítrico/biossíntese , Sporothrix/imunologia , Esporotricose/imunologia , Animais , Parede Celular , Ativação Enzimática , Inflamassomos/imunologia , Interleucina-17/biossíntese , Interleucina-18/biossíntese , Interleucina-1beta/biossíntese , Masculino , Camundongos , Camundongos Endogâmicos BALB C , Pele/microbiologia , Pele/patologiaRESUMO
We synthesized a series of novel dapsone-thalidomide hybrids (3a-i) by molecular hybridization and evaluated their potential for the treatment of type 2 leprosy reactions. All of the compounds had analgesic properties. Compounds 3c and 3h were the most active antinociceptive compounds and reduced acetic acid-induced abdominal constrictions by 49.8% and 39.1%, respectively. The hybrid compounds also reduced tumor necrosis factor-α levels in lipopolysaccharide-stimulated L929 cells. Compound 3i was the most active compound; at concentrations of 15.62 and 125 µM, compound 3i decreased tumor necrosis factor-α levels by 86.33% and 87.80%, respectively. In nude mice infected with Mycobacterium leprae in vivo, compound 3i did not reduce the number of bacilli compared with controls. Compound 3i did not have mutagenic effects in Salmonella typhimurium strains TA100 and TA102, with or without metabolic activation (S9 mixture). Our results indicate that compound 3i is a novel lead compound for the treatment of type 2 leprosy reactions.
Assuntos
Antibacterianos/síntese química , Antibacterianos/farmacologia , Dapsona/farmacologia , Hanseníase/tratamento farmacológico , Mycobacterium leprae/efeitos dos fármacos , Talidomida/farmacologia , Animais , Antibacterianos/química , Linhagem Celular , Dapsona/química , Relação Dose-Resposta a Droga , Humanos , Camundongos , Camundongos Nus , Testes de Sensibilidade Microbiana , Estrutura Molecular , Relação Estrutura-Atividade , Talidomida/químicaRESUMO
We synthesized a series of novel dapsone-thalidomide hybrids (3a-i) by molecular hybridization and evaluated their potential for the treatment of type 2 leprosy reactions. All of the compounds had analgesic properties. Compounds 3c and 3h were the most active antinociceptive compounds and reduced acetic acid-induced abdominal constrictions by 49.8% and 39.1%, respectively. The hybrid compounds also reduced tumor necrosis factor-α levels in lipopolysaccharide-stimulated L929 cells. Compound 3i was the most active compound; at concentrations of 15.62 and 125 µM, compound 3i decreased tumor necrosis factor-α levels by 86.33% and 87.80%, respectively. In nude mice infected with Mycobacterium leprae in vivo, compound 3i did not reduce the number of bacilli compared with controls. Compound 3i did not have mutagenic effects in Salmonella typhimurium strains TA100 and TA102, with or without metabolic activation (S9 mixture). Our results indicate that compound 3i is a novel lead compound for the treatment of type 2 leprosy reactions.
Assuntos
Humanos , Animais , Camundongos , Relação Estrutura-Atividade , Talidomida/química , Estrutura Molecular , Linhagem Celular , Dapsona/farmacologia , Dapsona/química , Relação Dose-Resposta a Droga , Hanseníase/tratamento farmacológico , Antibacterianos/síntese química , Antibacterianos/farmacologia , Antibacterianos/química , Mycobacterium leprae/efeitos dos fármacosRESUMO
Palladium(II) complexes are an important class of cyclopalladated compounds that play a pivotal role in various pharmaceutical applications. Here, we investigated the antitumour, anti-inflammatory, and mutagenic effects of two complexes: [Pd(dmba)(Cl)tu] (1) and [Pd(dmba)(N3)tu] (2) (dmba = N,N-dimethylbenzylamine and tu = thiourea), on Ehrlich ascites tumour (EAT) cells and peritoneal exudate cells (PECs) from mice bearing solid Ehrlich tumour. The cytotoxic effects of the complexes on EAT cells and PECs were assessed using the 3-(4,5-dimethylthiazol-3-yl)-2,5-diphenyl-tetrazolium bromide (MTT) assay. The effects of the complexes on the immune system were assessed based on the production of nitric oxide (NO) (Griess assay) and tumour necrosis factor-alpha (TNF-alpha), interleukin-12 (IL-12), and interleukin-10 (IL-10) (ELISA). Finally the mutagenic activity was assessed by the Ames test using the Salmonella typhimurium strain TA 98. Cisplatin was used as a standard. The IC50 ranges for the growth inhibition of EAT cells and PECs were found to be (72.8 +/- 3.23) microM and (137.65 +/- 0.22) microM for 1 and (39.7 +/- 0.30) microM and (146.51 +/- 2.67) microM for 2, respectively. The production of NO, IL-12, and TNF-alpha, but not IL-10, was induced by both complexes and cisplatin. The complexes showed no mutagenicity in vitro, unlike cisplatin, which was mutagenic in the strain. These results indicate that the complexes are not mutagenic and have potential immunological and antitumour activities. These properties make them promising alternatives to cisplatin.
Assuntos
Anti-Inflamatórios/farmacologia , Antineoplásicos/farmacologia , Carcinoma de Ehrlich/patologia , Paládio/farmacologia , Animais , Linhagem Celular Tumoral , Camundongos , Óxido Nítrico/metabolismoRESUMO
Sporotrichosis is a subcutaneous mycosis that is caused by the dimorphic fungus Sporothrix schenckii. This disease generally occurs within the skin and subcutaneous tissues, causing lesions that can spread through adjacent lymphatic vessels and sometimes leading to systemic diseases in immunocompromised patients. Macrophages are crucial for proper immune responses against a variety of pathogens. Furthermore, macrophages can play different roles in response to different microorganisms and forms of activation, and they can be divided into "classic" or "alternatively" activated populations, as also known as M1 and M2 macrophages. M1 cells can lead to tissue injury and contribute to pathogenesis, whereas M2 cells promote angiogenesis, tissue remodeling, and repair. The aim of this study was to investigate the roles of M1 and M2 macrophages in a sporotrichosis model. Toward this end, we performed phenotyping of peritoneal exudate cells and evaluated the concomitant production of several immunomediators, including IL-12, IL-10, TGF-ß, nitric oxide, and arginase-I activity, which were stimulated ex vivo with cell wall peptide-polysaccharide. Our results showed the predominance of the M2 macrophage population, indicated by peaks of arginase-I activity as well as IL-10 and TGF-ß production during the 6th and 8th weeks after infection. These results were consistent with cellular phenotyping that revealed increases in CD206-positive cells over this period. This is the first report of the participation of M2 macrophages in sporotrichosis infections.
Assuntos
Antígenos de Fungos/imunologia , Parede Celular/imunologia , Macrófagos/imunologia , Peptídeos/imunologia , Polissacarídeos/imunologia , Sporothrix/imunologia , Esporotricose/imunologia , Animais , Líquido Ascítico/citologia , Modelos Animais de Doenças , Exsudatos e Transudatos/citologia , Imunofenotipagem , Ativação de Macrófagos , Macrófagos/química , Macrófagos/classificação , Masculino , CamundongosRESUMO
PURPOSE: Soy and its fermented products are considered functional foods. The study objective was to assess three functional food - a non-fermented soy product (NFP), fermented soy product (FSP), fermented soy product enriched with isoflavones (FI) - in terms of their ability to reduce the development of adenocarcinoma in mice, as well their ability on modulating immune system. METHODS: It was observed tumor volume and to verify correlations with the immune system it was measured levels of the cytokines IL-1ß and TNF-α produced by macrophages as well as IFN-γ produced by lymphocytes using ELISA test, and nitric oxide production by macrophages using Griess reagent. RESULTS: All products showed immunological activity, but FSP showed the most effective tumor containment, resulting in smallest tumor volumes. FI animals expressed larger amounts of nitric oxide and IL-1ß and exhibited larger tumor sizes than FSP and NFP animals. CONCLUSIONS: The results suggested that the ingestion of FSP was most efficient in tumor containment, possibly due to a positive modulation of the immune system by when Enterococcus faecium and Lactobacillus helveticus are added to the soy product.
Assuntos
Adenocarcinoma/dietoterapia , Antineoplásicos/farmacologia , Neoplasias da Mama/dietoterapia , Enterococcus faecium , Glycine max/microbiologia , Lactobacillus helveticus , Adenocarcinoma/imunologia , Adenocarcinoma/metabolismo , Animais , Neoplasias da Mama/imunologia , Neoplasias da Mama/metabolismo , Feminino , Fermentação , Interferon gama/metabolismo , Interleucina-1beta/metabolismo , Camundongos , Camundongos Endogâmicos BALB C , Óxido Nítrico/metabolismo , Fator de Necrose Tumoral alfa/metabolismoRESUMO
BACKGROUND: Ribosome-inactivating proteins (RIP) have been studied in the search for toxins that could be used as immunotoxins for cancer treatment. Pulchellin, a type 2 RIP, is suggested to induce immune responses that have a role in controlling cancer. METHODS: The percentage of dendritic cells and CD4(+) and CD8(+) T cells in the spleen (flow cytometry), cytokines' release by PECs and splenocytes (ELISA) and nitric oxide production by PECs (Griess assay) were determined from tumor-bearing mice injected intratumorally with 0.1 ml of pulchellin at 0.75 µg/kg of body weight. Statistical analysis was performed by one-way ANOVA with Tukey's post hoc test. RESULTS: Pulchellin-treated mice showed significant immune system activation, characterized by increased release of IFN-γ and Th2 cytokines (IL-4 and IL-10), while IL-6 and TGF-ß levels were decreased. There was also an increase in macrophage's activation, as denoted by the higher percentage of macrophages expressing adhesion and costimulatory molecules (CD54 and CD80, respectively). CONCLUSIONS: Our results suggest that pulchellin is promising as an adjuvant in breast cancer treatment.
Assuntos
Abrus/química , Neoplasias da Mama/tratamento farmacológico , Neoplasias da Mama/imunologia , Proteínas de Plantas/administração & dosagem , Proteínas Inativadoras de Ribossomos Tipo 2/administração & dosagem , Animais , Linfócitos T CD8-Positivos/imunologia , Linhagem Celular Tumoral , Citocinas/imunologia , Feminino , Humanos , Macrófagos/efeitos dos fármacos , Camundongos , Camundongos Endogâmicos BALB C , Baço/imunologia , Células Th2/imunologiaRESUMO
Sporotrichosis is often manifested as a chronic granulomatous infection and the monocytes/macrophages play a central role in the host defense system. Surface components of Sporothrix schenckii have been characterized and suggestions have been made as to their possible role in pathogenicity. Ergosterol peroxide, cell-wall compounds (alkali-insoluble fraction-F1 and lipid extract-LEY), and exoantigen from the yeast form of the fungus have been characterized as virulence factors, activating both innate, by cytotoxins linked to the activation of reactive oxygen and nitrogen species (H2O2 and NO), and adaptive immune response to produce cytokines Th1 and Th2 profile. In this study, preliminary results have demonstrated that, in systemic sporotrichosis, TLR-4 triggers the innate immune response, activating an oxidative burst. These data represent the first report of the participation of TLR-4 in murine sporotrichosis, in the presence of lipids from the cell wall of S. schenckii. These results taken together may open new perspectives of study leading to an antifungal agent that could be used to benefit the entire population.
Assuntos
Sporothrix/imunologia , Esporotricose/imunologia , Animais , Parede Celular/imunologia , Peróxido de Hidrogênio/metabolismo , Macrófagos Peritoneais/imunologia , Camundongos , Camundongos Endogâmicos C3H , Explosão Respiratória/imunologia , Esporotricose/microbiologia , Receptor 4 Toll-Like/imunologiaRESUMO
Mycobacterium tuberculosis is responsible for over 8 million cases of tuberculosis (TB) annually. Natural products may play important roles in the chemotherapy of TB. The immunological activity of Davilla elliptica chloroform extract (DECE) was evaluated in vitro by the determination of hydrogen peroxide (H2O2), nitric oxide (NO), and tumor necrosis factor-alpha (TNF-alpha) release in peritoneal macrophages cultures. DECE was also tested for its antimycobacterial activity against M. tuberculosis using the microplate alamar blue assay. DECE (50, 150, 250 mug/ml) stimulated the production of H2O2 (from 1,79 ± 0,23 to 7,27 ± 2,54; 15,02 ± 2,86; 20,5 ± 2,1 nmols) (means ± SD), NO (from 2,64 ± 1,02 to 25,59 ± 2,29; 26,68 ± 2,41; 29,45 ± 5,87 mumols) (means ± SD) and TNF-alpha (from 2,44 ± 1,46 to 30,37 ± 8,13; 38,68 ± 1,59; 41,6 ± 0,90 units/ml) (means ± SD) in a dose-dependent manner and also showed a promising antimycobacterial activity with a minimum inhibitory concentration of 62,5 mug/ml. This plant may have therapeutic potential in the immunological and microbiological control of TB.
Assuntos
Animais , Camundongos , Antibióticos Antituberculose/farmacologia , Dilleniaceae/química , Macrófagos/microbiologia , Mycobacterium tuberculosis/efeitos dos fármacos , Antibióticos Antituberculose/isolamento & purificação , Peróxido de Hidrogênio/metabolismo , Testes de Sensibilidade Microbiana , Macrófagos/metabolismo , Óxido Nítrico/biossíntese , Extratos Vegetais/farmacologia , Fator de Necrose Tumoral alfa/biossínteseRESUMO
In an attempt to elucidate the effects of Sporothrix schenckii infection on the immune response, our laboratory has developed a murine model of disseminated sporotrichosis. Helper T cells can be further subdivided into Th1 and Th2 phenotypes. The differentiation of two subsets of T lymphocytes is driven by IL-12 and IL-4 cytokines, respectively. Th1 cells produce IFN-gamma that activate macrophages and promote cell-mediated immunity. In addition, we found low levels of iNOS and NO production in the initial (1st and 2nd weeks) and final (9th and 10th weeks) periods of the infection, in contrast with the period of week 4 to 7 of elevated values. The determination of IFN-gamma and IL-12 are in agreement with NO/iNOS detection, showing the presence of cellular immune response throughout the infectious process. However, the production of IL-4 shows an increase in levels after the 5th and 6th weeks suggesting a participation of Th2 response in this period as well. Regarding these results, the study demonstrated that in experimental sporotrichosis infection the cellular immune response participated throughout the period analyzed as a nitric oxide dependent mechanism. In contrast, the presence of Th2 response began in the 5th week, suggesting the participation of humoral immune response in advanced stages of sporotrichosis.
Assuntos
Óxido Nítrico/imunologia , Sporothrix/imunologia , Esporotricose/imunologia , Células Th1/imunologia , Células Th2/imunologia , Animais , Interferon gama/imunologia , Interleucina-12/imunologia , Subunidade p40 da Interleucina-12 , Interleucina-4/imunologia , Fígado/imunologia , Fígado/microbiologia , Macrófagos Peritoneais/imunologia , Macrófagos Peritoneais/microbiologia , Masculino , Camundongos , Óxido Nítrico Sintase Tipo II/imunologia , Subunidades Proteicas/imunologia , Baço/imunologia , Baço/microbiologiaRESUMO
As respostas imunes säo mediadas por uma variedade de células e por moléculas que estas células secretam. Macrófagos säo as primeiras células a participarem da resposta imunológica, e quando säo ativados liberam mais de cem compostos no meio extracelular, entre eles várias citocinas(TNF-alfa) e compostos reativos intermediários de nitrogênio (NO). Neste trabalho, determinou-se a liberaçäo de óxido nítrico e TNF-alfa em culturas de macrófagos peritoneais de camundongos em presença de extrato etanólico 70 por cento bruto obtido a partir de flores de Melampodium divaricatum (Asteraceae) nas concentraçöes de 20, 10 e 5mg/ml. O extrato etanólico 70 por cento bruto de Melampodium divaricatum (flores) induziu grande liberaçäo de NO e TNF-alfa na concentraçäo de 20 mg/ml quando comparado com LPS. Concluiu-se que esse extrato é um potente estimulador de macrófagos, podendo apresentar atividade imunomoduladora.
Assuntos
Animais , Feminino , Camundongos , Asteraceae , Ativação de Macrófagos , Macrófagos Peritoneais , Óxido Nítrico , Extratos Vegetais , Fator de Necrose Tumoral alfaRESUMO
A alfa-1-antitripsina (Ó1-AT) é uma proteína de fase aguda, sendo a mais importante de várias antiproteases, pois atua como protetora contra injúrias nos tecidos. Ela migra eletroforeticamente na regiäo das alfa-globulinas. Neste trabalho foram analisadas amostras de soros de pacientes portadores de infecçöes crônicas por parasitas e bactérias quanto à verificaçäo do fenótipo de Ó1-AT, caracterizado por focalizaçäo isoelétrica, e à sua determinaçäo quantitativa mediante a capacidade de inibiçäo da tripsina. Tanto os fenótipos quanto as dosagens de Ó1-AT inseriram-se dentro dos valores normais estabelecidos para estas metodologias. Estes resultados demonstraram que näo houve correlaçäo entre as patologias analisadas e o nível deste mediador do processo inflamatório. Provavelmnente, outros fatores do hospedeiro, tais como a imunomodulaçäo por citocinas, participaçäo de anticorpos e linfócitos T citotóxicos, estejam envolvidos na cronicidade destas infecçöes.