Beta amyloid precursor protein and patterns of HIV p24 immunohistochemistry in different brain areas of AIDS patients

AIDS. 2001 Mar 30;15(5):571-5. doi: 10.1097/00002030-200103300-00005.

Abstract

Objectives: To evaluate the correlation between immunohistochemical positive patterns (globular and filamentous structures) of beta-amyloid precursor protein (beta-APP), used as a marker of axonal damage, and the different distribution of HIV p24 antigens, in three different brain areas of AIDS patients.

Methods: Eighteen AIDS patients with HIV-related brain lesions were included in the study. Forty-nine sections from basal ganglia, frontal cortex and hippocampus were selected. After microwave oven pre-treatment, the sections were incubated with anti-HIV p24 and anti-beta-APP monoclonal antibodies; the reactions were developed with peroxidase/3,3'diaminobenzidine. The positivity was graded by semi-quantitative scores. Double immunohistochemical staining was used to evaluate the co-localization of the antigens.

Results: HIV p24 immunohistochemistry was positive in 44 of 49 sections (89%), with a prevalence of interstitial positive cells and positive microglial nodules in 27 and 13 sections respectively. beta-APP-positive structures were demonstrated in 23 of 44 sections (52%) with HIV-related lesions, and were absent from the five sections without viral expression. Globular and filamentous lesions were observed in 21 of 23 sections and 10 of 23 lesions respectively. Moreover, a high grade of globular type lesion was related to an elevated presence of diffuse interstitial HIV p24-positive cells in basal ganglia; double immunohistochemical reactions demonstrated the co-localization of beta-APP globules and HIV p24 antigens.

Conclusions: The data obtained confirm the coexpression of beta-APP and viral antigens in particular areas of the brain with HIV-related lesions; there is a strict correlation between beta-APP globules (indicating chronic cerebral damage) and the interstitial pattern of HIV p24 immunohistochemistry.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acquired Immunodeficiency Syndrome / epidemiology
  • Acquired Immunodeficiency Syndrome / metabolism*
  • Acquired Immunodeficiency Syndrome / pathology
  • Acquired Immunodeficiency Syndrome / virology
  • Amyloid beta-Protein Precursor / metabolism*
  • Basal Ganglia / metabolism*
  • Basal Ganglia / pathology
  • Basal Ganglia / virology
  • Biomarkers
  • Frontal Lobe / metabolism*
  • Frontal Lobe / pathology
  • Frontal Lobe / virology
  • HIV Core Protein p24 / metabolism*
  • HIV-1*
  • Hippocampus / metabolism*
  • Hippocampus / pathology
  • Hippocampus / virology
  • Humans
  • Italy / epidemiology
  • Retrospective Studies

Substances

  • Amyloid beta-Protein Precursor
  • Biomarkers
  • HIV Core Protein p24