AIDS dementia complex and HIV‐1 brain infection: Clinical‐virological correlations

Bruce J. Brew, Marc K. Rosenblum, Kathy A. Cronin, Richard W. Price

Annals of Neurology · 1995 · 259 citations · 60 references

Concepts

TL;DR

The study aimed to map HIV‑1 p24 core protein distribution in the brains of 55 AIDS autopsy cases to assess central nervous system infection. Immunohistochemistry was used to map HIV‑1 p24 in brain tissue, and in 40 patients with prior neurological assessment, the extent of viral infection was correlated with AIDS dementia complex severity. HIV‑1 antigen was found mainly in macrophages, microglia, and multinucleated cells within deep brain structures, and its presence correlated with multinucleated‑cell encephalitis and ADC stage, yet only 61 % of stage 1 patients showed antigen and about 30 % of sections were positive, indicating that limited infection combined with toxin amplification may drive ADC.

Abstract

Abstract To evaluate the presence and distribution of central nervous system infection by human immunodeficiency virus type 1 (HIV‐1), we used immunohistochemical methods to map the HIV‐1 p24 core protein in the brains of 55 autopsied patients with acquired immunodeficiency syndrome (AIDS). In a subset of 40 of these patients who had undergone antemortem neurological evaluation of the AIDS dementia complex (ADC), we analyzed the relation between the severities of the viral infection and clinical dysfunction. Viral antigen was detected in macrophages and cells with morphological and immunohistochemical characteristics of microglia as well as multinucleated cells. The distribution of antigen‐positive cells preferentially involved certain deep brain structures, especially the globus pallidus, other basal ganglia nuclei, and the central white matter. Overall, the presence and frequency of infected cells were highly correlated with the histological findings of multinucleated‐cell encephalitis and in general with the clinical ADC stage. However, infection was often more limited than might be “anticipated” from the severity of patients' clinical dysfunction: Only 61% of patients with at least ADC stage 1 had detectable antigen and of these only approximately 30% of the brain sections were antigen positive. These results suggest a pathogenetic model of ADC where virus‐ or cell‐coded toxins amplify the effect of limited brain infection.

References

60