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2.
Microbiol Res ; 163(5): 579-85, 2008.
Artigo em Inglês | MEDLINE | ID: mdl-16962755

RESUMO

The increase in the number of infections caused by Candida species and the consequent use of antifungal agents favours an increase of resistant isolates. The aim of this study was to evaluate the antifungal susceptibility of Candida spp. isolates from patients with different systemic predisposing factors to candidosis. Seventy-nine Candida spp. isolates were assayed for in vitro susceptibility to amphotericin B, fluconazole, 5-flucytosine and itraconazole using the technique proposed by the Clinical and Laboratory Standards Institute (CLSI). Four C. albicans, one C. guilliermondii, four C. parapsilosis and two C. tropicalis isolates were resistant to amphotericin B. Only two isolate was resistant to itraconazole. All the isolates tested were susceptible to fluconazole and flucytosine. It could be concluded that the most efficient drugs against the Candida isolates studied were fluconazole and flucytosine and that all of the antifungal agents used in this study were effective against the Candida spp. isolates tested.


Assuntos
Antifúngicos/farmacologia , Candida/efeitos dos fármacos , Candidíase/microbiologia , Candida/isolamento & purificação , Candidíase/tratamento farmacológico , Candidíase/etiologia , Suscetibilidade a Doenças , Farmacorresistência Fúngica , Feminino , Humanos , Masculino , Testes de Sensibilidade Microbiana
3.
Trop Med Infect Dis ; 3(4)2018 Nov 21.
Artigo em Inglês | MEDLINE | ID: mdl-30469320

RESUMO

Schistosomiasis, a disease historically associated with poverty, lack of sanitation and social inequality, is a chronic, debilitating parasitic infection, affecting hundreds of millions of people in endemic countries. Although chemotherapy is capable of reducing morbidity in humans, rapid re-infection demonstrates that the impact of drug treatment on transmission control or disease elimination is marginal. In addition, despite more than two decades of well-executed control activities based on large-scale chemotherapy, the disease is expanding in many areas including Brazil. The development of the Sm14/GLA-SE schistosomiasis vaccine is an emblematic, open knowledge innovation that has successfully completed phase I and phase IIa clinical trials, with Phase II/III trials underway in the African continent, to be followed by further trials in Brazil. The discovery and experimental phases of the development of this vaccine gathered a robust collection of data that strongly supports the ongoing clinical phase. This paper reviews the development of the Sm14 vaccine, formulated with glucopyranosyl lipid A (GLA-SE), from the initial experimental developments to clinical trials including the current status of phase II studies.

4.
Vaccine ; 34(4): 586-594, 2016 Jan 20.
Artigo em Inglês | MEDLINE | ID: mdl-26571311

RESUMO

DESIGN: Safety and immunogenicity of a recombinant 14kDa, fatty acid-binding protein(FABP) from Schistosoma mansoni (rSm14) were evaluated through an open, non-placebo-controlled, dose-standardized trial, performed at a single research site. The vaccine was formulated with glucopyranosyl lipid A (GLA) adjuvant in an oil-in-water emulsion (SE) and investigated in 20 male volunteers from a non-endemic area for schistosomiasis in the state of Rio de Janeiro, Brazil. Fifty microgram rSm14 with 10 µg GLA-SE (rSm14/GLA-SE)/dose were given intramuscularly three times with 30-day intervals. Participants were assessed clinically, biochemically and immunologically for up to 120 days. METHODS: Participants were screened for inclusion by physical examination, haematology and blood chemistry; then followed to assess adverse events and immunogenicity. Sera were tested for IgG (total and isotypes) and IgE. T cell induction of cytokines IL-2, IL-5, IL-10, IFNγ and TNFα was assessed by Milliplex kit and flow cytometry. RESULTS: The investigational product showed high tolerability; some self-limited, mild adverse events were observed during and after vaccine administration. Significant increases in Sm14-specific total IgG, IgG1 and IgG3 were observed 30 days after the first vaccination with specific IgG2 and IgG4 after 60 days. An increase in IgE antibodies was not observed at any time point. The IgG response was augmented after the second dose and 88% of all vaccinated subjects had developed high anti-Sm14 IgG titres 90 days after the first injection. From day 60 and onwards, there was an increase in CD4(+) T cells producing single cytokines, particularly TNFα and IL-2, with no significant increase of multi-functional TH1 cells. CONCLUSION: Clinical trial data on tolerability and specific immune responses after vaccination of adult, male volunteers in a non-endemic area for schistosomiasis with rSm14/GLA-SE, support this product as a safe, strongly immunogenic vaccine against schistosomiasis paving the way for follow-up Phase 2 trials. Study registration ID: NCT01154049 at http://www.clinicaltrials.gov.


Assuntos
Proteínas de Ligação a Ácido Graxo/imunologia , Proteínas de Helminto/imunologia , Schistosoma mansoni , Esquistossomose/prevenção & controle , Vacinas/uso terapêutico , Adjuvantes Imunológicos/administração & dosagem , Adolescente , Adulto , Animais , Anticorpos Anti-Helmínticos/sangue , Brasil , Citocinas/imunologia , Humanos , Imunoglobulina G/sangue , Masculino , Pessoa de Meia-Idade , Linfócitos T/imunologia , Vacinas/efeitos adversos , Vacinas/imunologia , Adulto Jovem
7.
Mem Inst Oswaldo Cruz ; 99(2): 147-52, 2004 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-15250467

RESUMO

The patterns of genetic variation of samples of Candida spp. isolated from patients infected with human immunodeficiency virus in Vitória, state of Espírito Santo, Brazil, were examined. Thirty-seven strains were isolated from different anatomical sites obtained from different infection episodes of 11 patients infected with the human immunodeficiency virus (HIV). These samples were subjected to randomly amplified polymorphic DNA (RAPD) analysis using 9 different primers. Reproducible and complex DNA banding patterns were obtained. The experiments indicated evidence of dynamic process of yeast colonization in HIV-infected patients, and also that certain primers are efficient in the identification of species of the Candida genus. Thus, we conclude that RAPD analysis may be useful in providing genotypic characters for Candida species typing in epidemiological investigations, and also for the rapid identification of pathogenic fungi.


Assuntos
Candida/genética , DNA Fúngico/genética , Variação Genética , Infecções Oportunistas Relacionadas com a AIDS/microbiologia , Sequência de Bases , Candida/isolamento & purificação , Candidíase/microbiologia , Amplificação de Genes , Genótipo , Humanos , Dados de Sequência Molecular , Técnica de Amplificação ao Acaso de DNA Polimórfico
8.
Can J Microbiol ; 50(7): 514-20, 2004 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-15381977

RESUMO

PCR was used to amplify a targeted region of the ribosomal DNA of 76 Candida spp. isolates from immunocompromised and seriously diseased patients. Thirty-seven strains isolated from different anatomical sites of 11 patients infected with HIV (Vitória, ES, Brazil), 26 isolates from patients under treatment at Odilon Behrens Hospital and 13 isolates from skin and urine samples from São Marcos Clinical Analysis Laboratory (Belo Horizonte, Brazil) were scored. Fragments of rDNA were amplified using primer pairs ITS1-ITS4, for the amplification of ITS1 and ITS2 regions, including the gene for the 5.8 s subunit. Amplification resulted in fragments ranging in size from 350 to 950 bp. Amplicons were digested with eight restriction enzymes. A pattern of species-specificity among the different medically important Candida species could be identified following restriction digestion of the PCR products. Candida albicans was the species most frequently observed, except for the group of newborns under treatment at the Odilon Behrens Hospital and for the isolates from the clinical analysis laboratory. C. parapsilosis was the species most frequently observed in these two groups.


Assuntos
Candida/classificação , Candida/isolamento & purificação , Candidíase/microbiologia , DNA Ribossômico/análise , Hospedeiro Imunocomprometido , Polimorfismo de Fragmento de Restrição , Candida/genética , Candida albicans/classificação , Candida albicans/genética , Candida albicans/isolamento & purificação , Análise por Conglomerados , Impressões Digitais de DNA , Enzimas de Restrição do DNA/metabolismo , DNA Fúngico/análise , DNA Fúngico/isolamento & purificação , DNA Ribossômico/isolamento & purificação , DNA Ribossômico/metabolismo , DNA Espaçador Ribossômico/isolamento & purificação , DNA Espaçador Ribossômico/metabolismo , Genes de RNAr , Humanos , Epidemiologia Molecular , Técnicas de Tipagem Micológica , Filogenia , Reação em Cadeia da Polimerase , RNA Ribossômico 5,8S/genética
9.
Mem. Inst. Oswaldo Cruz ; 99(2): 147-152, Mar. 2004. ilus, tab
Artigo em Inglês | LILACS | ID: lil-360967

RESUMO

The patterns of genetic variation of samples of Candida spp. isolated from patients infected with human immunodeficiency virus in Vitória, state of Espírito Santo, Brazil, were examined. Thirty-seven strains were isolated from different anatomical sites obtained from different infection episodes of 11 patients infected with the human immunodeficiency virus (HIV). These samples were subjected to randomly amplified polymorphic DNA (RAPD) analysis using 9 different primers. Reproducible and complex DNA banding patterns were obtained. The experiments indicated evidence of dynamic process of yeast colonization in HIV-infected patients, and also that certain primers are efficient in the identification of species of the Candida genus. Thus, we conclude that RAPD analysis may be useful in providing genotypic characters for Candida species typing in epidemiological investigations, and also for the rapid identification of pathogenic fungi.


Assuntos
Humanos , Candida , DNA Fúngico , Variação Genética , Infecções Oportunistas Relacionadas com a AIDS , Sequência de Bases , Candida , Candidíase , Amplificação de Genes , Genótipo , Dados de Sequência Molecular , Técnica de Amplificação ao Acaso de DNA Polimórfico
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