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Detection of Human Immunodeficiency Virus Core Protein in Plasma by Enzyme Immunoassay

Annals of Internal MedicinePublished 1 September 1987
Alec E. Wittek, MICHAEL A. PHELAN, MARTHA A. WELLS, LUBA K. VUJCIC, JAY S. EPSTEIN, H. CLIFFORD LANE
Citations51
SJR quartileQ1
SJR score3.38
SNIP3.27

TL;DR

A sensitive enzyme immunoassay was developed for detecting human immunodeficiency virus (HIV) core antigen and antigenemia was associated with reduced T-cell number and symptomatic disease, and may be a useful marker for disease progression.

Abstract

A sensitive enzyme immunoassay was developed for detecting human immunodeficiency virus (HIV) core antigen. Assay sensitivity was 3.67 pmol/L of purified HIV core protein, and 1 or 100 in-vitro infectious units/mL of HIV in purified virus preparations or cell culture supernatants, respectively. Enzyme immunoassay sensitivity exceeded that of reverse transcriptase assay by 1000-fold. Core antigen was detected in whole plasma from 41% of symptomatic subjects and 13% of asymptomatic subjects seropositive for HIV. After plasma fractionation, antigenemia was found in 60% of symptomatic subjects and in 33% of asymptomatic subjects seropositive for HIV. Fifty-seven percent of samples from which HIV could be isolated in lymphocyte culture had detectable quantities of core antigen in plasma. However, at least 87% of samples with measurable antigen in plasma had HIV isolated from lymphocyte cultures. Antigenemia was associated with reduced T-cell number and symptomatic disease, and may be a useful marker for disease progression.

Keywords

Immunology and MicrobiologyMedicine