Detection of Human Immunodeficiency Virus Core Protein in Plasma by Enzyme Immunoassay
Association of Antigenemia with Symptomatic Disease and T-Helper Cell Depletion
- ALEC E. WITTEK, M.D., C.M.;
- MICHAEL A. PHELAN, Ph.D.;
- MARTHA A. WELLS, B.S.;
- LUBA K. VUJCIC, M.S.;
- JAY S. EPSTEIN, M.D.;
- H. CLIFFORD LANE, M.D.; and
- GERALD V. QUINNAN, Jr., M.D.
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.
Article and Author Information
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▸From the Division of Virology, Office of Biologics Research and Review, Food and Drug Administration, and Laboratory of Immunoregulation, National Institute of Allergy and Infectious Diseases; Bethesda, Maryland.
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▸Requests for reprints should be addressed to Alec E. Wittek, M.D.; Division of virology, HFN-840, Office of Biologics Research and Review, 8800 Rockville Pike; Bethesda, MD 20892.
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