Characterization of cytokine gene expression associated with noninfectious human immunodeficiency virus retinopathy in human autopsy eyes

Retina. 2010 Jun;30(6):952-7. doi: 10.1097/IAE.0b013e3181c700f8.

Abstract

Purpose: The purpose of this study was to determine the cytokine-related pathogenesis of human immunodeficiency virus retinopathy in human autopsy eyes.

Methods: Fresh autopsy eyes were procured from clinically diagnosed patients with acquired immunodeficiency syndrome who had died as a result of disease-related complications; eyes were immediately immersed in RNAlater. Clean 2-mm trephines were used to punch individual pathologic retina in areas of cotton-wool spots and control punches. Total RNA was extracted using the TRIzol extraction protocol, and the optimal density of the RNA was measured at an optical density of 260 nm. [Delta]Ct (cytokine) values were calculated using the comparative cytokine analysis method. The results are expressed as a mean fold modulation and as a statistical comparison of Ct values controlling for retinal areas without a lesion in the same eye.

Results: The fold modulations and the statistical comparisons of the cytokines studied in tissues from cotton-wool spots and control retina, respectively, regulated on activation normal T cell expressed and secreted (RANTES), macrophage inflammatory protein 1beta, macrophage inflammatory protein 1alpha (5.32x, P = 0.04), and Bcl-2-associated X protein (1.24x, P = 0.05) had a marked elevation of fold modulation and were statistically significant compared with control tissue. Interleukin-8 (1.09x, P = 0.18), interleukin-4, and interleukin-10 (2.7x, P = 0.30) were not significantly expressed in cotton-wool spots.

Conclusion: Certain inflammatory human immunodeficiency virus-associated and apoptotic cytokines are expressed in cotton-wool spots in eyes with human immunodeficiency virus retinopathy.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Autopsy
  • CD4 Lymphocyte Count
  • CD4-Positive T-Lymphocytes / immunology
  • Chemokine CCL3 / metabolism
  • Chemokine CCL4 / metabolism
  • Chemokine CCL5 / metabolism
  • Cytokines / genetics*
  • Eye Infections, Viral / genetics*
  • Eye Infections, Viral / virology
  • Gene Expression Regulation / physiology*
  • HIV Infections / genetics*
  • HIV Infections / virology
  • Humans
  • Middle Aged
  • RNA, Messenger / genetics
  • Real-Time Polymerase Chain Reaction
  • Retinal Diseases / genetics*
  • Retinal Diseases / virology
  • bcl-2-Associated X Protein / metabolism

Substances

  • Chemokine CCL3
  • Chemokine CCL4
  • Chemokine CCL5
  • Cytokines
  • RNA, Messenger
  • bcl-2-Associated X Protein