Abstract | INTRODUCTION: METHODS: Blood samples (5 mL) 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.
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Authors | Antonio Carlos Rosário Vallinoto, Felipe Bonfim Freitas, Isabella Guirelli, Luiz Fernando Almeida Machado, Vânia Nakauth Azevedo, Izaura Cayres-Vallinoto, Marluísa Oliveira Guimarães Ishak, Ricardo Ishak |
Journal | Revista da Sociedade Brasileira de Medicina Tropical
(Rev Soc Bras Med Trop)
2011 Jan-Feb
Vol. 44
Issue 1
Pg. 1-3
ISSN: 1678-9849 [Electronic] Brazil |
PMID | 21340397
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
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Topics |
- Adult
- CD4 Lymphocyte Count
- Case-Control Studies
- HIV Infections
(blood, genetics, virology)
- HIV-1
(genetics)
- Humans
- Mannose-Binding Lectin
(blood, genetics)
- Polymerase Chain Reaction
- Polymorphism, Genetic
(genetics)
- Viral Load
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