M. Nebuloni et al., Beta amyloid precursor protein and patterns of HIV p24 immunohistochemistry in different brain areas of AIDS patients, AIDS, 15(5), 2001, pp. 571-575
Objectives: To evaluate the correlation between immunohistochemical positiv
e 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 pa
tients.
Methods: Eighteen AIDS patients with HIV-related brain lesions were include
d 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 pos
itivity 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 microglia
l 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 t
o an elevated presence of diffuse interstitial HIV p24-positive cells in ba
sal ganglia; double immunohistochemical reactions demonstrated the co-local
ization of beta -APP globules and HIV p24 antigens.
Conclusions: The data obtained confirm the coexpression of beta -APP and vi
ral antigens in particular areas of the brain with HIV-related lesions; the
re is a strict correlation between beta -APP globules (indicating chronic c
erebral damage) and the interstitial pattern oi HIV p24 immunohistochemistr
y. (C) 2001 Lippincott Williams & Wilkins.