May 2008
Volume 49, Issue 13
ARVO Annual Meeting Abstract  |   May 2008
Tnf- Gene Polymorphism in Patients With Toxoplasmic Retinochoroiditis
Author Affiliations & Notes
  • C. A. Cordeiro
    Uveitis, San Geraldo Hospital, Campos, Brazil
  • F. Orefice
    Uveitis, San Geraldo Hospital, Belo Horizonte, Brazil
  • W. R. Campos
    Uveitis, San Geraldo Hospital, Campos, Brazil
  • P. R. Moreira
    ICB, UFMG, Belo Horizonte, Brazil
  • A. L. Teixeira
    ICB, UFMG, Belo Horizonte, Brazil
  • W. O. Dutra
    ICB, UFMG, Belo Horizonte, Brazil
  • Footnotes
    Commercial Relationships  C.A. Cordeiro, None; F. Orefice, None; W.R. Campos, None; P.R. Moreira, None; A.L. Teixeira, None; W.O. Dutra, None.
  • Footnotes
    Support  None.
Investigative Ophthalmology & Visual Science May 2008, Vol.49, 5135. doi:
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      C. A. Cordeiro, F. Orefice, W. R. Campos, P. R. Moreira, A. L. Teixeira, W. O. Dutra; Tnf- Gene Polymorphism in Patients With Toxoplasmic Retinochoroiditis. Invest. Ophthalmol. Vis. Sci. 2008;49(13):5135. doi:

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      © ARVO (1962-2015); The Authors (2016-present)

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Purpose: : Considering the importance of TNF-α in pathogenesis of toxoplasmic retinochoroiditis (TR) and that the presence of this functional polymorphism affect the levels of cytokines produced, we aim to investigate the possible association between TNF-α (-308G/A) polymorphism and TR in humans.

Methods: : Cross-sectional study which included one hundred Brazilian patients meeting well-defined criteria for the diagnosis of TR and fifty age and gender matched control subjects with no signs of ocular toxoplasmosis in whom anti-toxoplasma antibody analysis revealed positive immunoglobulin G titers. Genomic DNA was obtained from oral swabs of all subjects and amplified using the polymerase chain reaction (PCR) with specific primers flanking the locus -308 of TNF-α. PCR products were submitted to restriction endonuclease digestion and analyzed by polyacrylamide gel electrophoresis, to distinguish alleles G and A of the TNF-α gene, allowing for the determination of the genotypes and detection of the polymorphism.

Results: : There was no significant difference in the genotype (x² = 0.79, P = 0.67), allele (x² = 0.095, P = 0.75), and allele carriage (x² = 0.70, P = 0.40) distribuitions in patients with TR compared with control subjects. Prevalences of the genotype (x² = 0.2.05, P = 0.35) and allele (x² = 0.13, P = 0.71) distribuitions did not significantly differ between with and without recurrence episode groups.

Conclusions: : This study is the first to study the association between the TNF-α polymorphism and occurrence of TR in humans. We demonstrated that the TNF-α (-308G/A) is not associated with occurrence or recurrence of TR.

Keywords: retinochoroiditis • immunomodulation/immunoregulation • inflammation 

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