Revista da Sociedade Brasileira de Medicina Tropical (Feb 2011)

Characterization of mannose-binding lectin plasma levels and genetic polymorphisms in HIV-1-infected individuals

  • 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

DOI
https://doi.org/10.1590/S0037-86822011000100001
Journal volume & issue
Vol. 44, no. 1
pp. 1 – 3

Abstract

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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 0.05). 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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