Navegando por Autor "FREITAS, Felipe Bonfim"

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Acesso aberto (Open Access)
Characterization of mannose-binding lectin plasma levels and genetic polymorphisms in HIV-1-infected individuals
(2011-02) VALLINOTO, Antonio Carlos Rosário; FREITAS, Felipe Bonfim; GUIRELLI, Isabella; MACHADO, Luiz Fernando Almeida; AZEVEDO, Vânia Nakauth; VALLINOTO, Izaura Maria Vieira Cayres; ISHAK, Marluísa de Oliveira Guimarães; ISHAK, Ricardo
INTRODUCTION: The present study investigated the association between mannose-binding lectin (MBL) gene polymorphism and serum levels with infection by HIV-1. METHODS: Blood samples (5mL) were collected from 97 HIV-1-infected individuals resident in Belém, State of Pará, Brazil, who attended the Special Outpatient Unit for Infections and Parasitic Diseases (URE-DIPE). CD4+ T-lymphocyte count and plasma viral load were quantified. A 349bp fragment of exon 1 of the MBL was amplified via PCR, using genomic DNA extracted from controls and HIV-1-infected individuals, following established protocols. MBL plasma levels of the patients were quantified using an enzyme immunoassay kit. RESULTS: Two alleles were observed: MBL*O, with a frequency of 26.3% in HIV-1-infected individuals; and the wild allele MBL*A (73.7%). Similar frequencies were observed in the control group (p > 0.05). Genotype frequencies were distributed according to the Hardy-Weinberg equilibrium in both groups. Mean MBL plasma levels varied by genotype, with statistically significant differences between the AA and AO (p < 0.0001), and AA and OO (p < 0.001) genotypes, but not AO and OO (p = 0.17). Additionally, CD4+ T-lymphocytes and plasma viral load levels did not differ significantly by genotype (p > 0.05). CONCLUSIONS: The results of this study do not support the hypothesis that MBL gene polymorphism or low plasma MBL concentrations might have a direct influence on HIV-1 infection, although a broader study involving a large number of patients is needed.
Acesso aberto (Open Access)
Clinical and pathological importance of vacA allele heterogeneity and cagA status in peptic ulcer disease in patients from North Brazil
(2005-12) MARTINS, Luisa Caricio; CORVELO, Tereza Cristina de Oliveira; DEMACHKI, Sâmia; ARAÚJO, Marialva Tereza Ferreira de; ASSUMPÇÃO, Mônica Baraúna de; VILAR, Simone Cristina Araujo Jucá; FREITAS, Felipe Bonfim; BARBOSA, Hivana Patricia Melo; FECURY, Amanda Alves; AMARAL, Renata Kelly Costa do; SANTOS, Sidney Emanuel Batista dos
We have examined the prevalence of gene cagA and vacA alleles in 129 patients, 69 with gastritis and 60 with peptic ulcer diseases from North Brazil and their relation with histopathological data. vacA and cagA genotype were determined by polymerase chain reaction. Hematoxylin-eosin staining was used for histological diagnosis. 96.6% of the patients were colonized by Helicobacter pylori strains harboring single vacA genotype (nont-mixed infection). Among them, 11.8% had subtype s1a, 67.8% had subtype s1b, and 17% subtype s2. In regard to the middle region analysis, m1 alleles were found in 75.4% and m2 in 21.2% of patients. The cagA gene was detected in 78% patients infected with H. pylori and was associated with the s1-m1 vacA genotype. The H. pylori strains, vacA s1b m1/cagA-positive, were associated with increased risk of peptic ulcer disease and higher amounts of lymphocytic and neutrophilic infiltrates and the presence of intestinal metaplasia. These findings show that cagA and vacA genotyping may have clinical relevance in Brazil.