Diagnosis of Human Immunodeficiency Virus Infection by Immunoassay Using a Molecularly Cloned and Expressed Virus Envelope Polypeptide
Comparison to Western Blot on 2707 Consecutive Serum Samples
- DONALD S. BURKE, M.D.;
- BRENDA L. BRANDT, M.S.;
- ROBERT R. REDFIELD, M.D.;
- TUN-HOU LEE, Ph.D.;
- RICHARD M. THORN, Ph.D.;
- GERALD A. BELTZ, Ph.D.; and
- CHUNG-HO HUNG, Ph.D.
Abstract
To detect human immunodeficiency virus (HIV) antibodies in a simple enzyme-linked immunoassay (CBre3-EIA), we used an Escherichia coli-expressed polypeptide antigen, representing the carboxy-terminal third of the external membrane glycoprotein gene fused with the amino-terminal half of the transmembrane glycoprotein gene. Over a 3-month period, 2707 consecutive serum samples referred for confirmatory testing for human T-lymphotrophic virus type III (HTLV-III) antibodies were evaluated by both Western blot and CBre3-EIA. On a single determination for each sample, the CBre3-EIA was found to have an estimated sensitivity (99.9%) and specificity (99.1%) similar or superior to the more cumbersome Western blot method. This study shows that all HIV-seropositive subjects have antibodies to the virus envelope protein; no other virus antigens are required for construction of highly sensitive immunoassays.
Article and Author Information
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▸From the Division of Communicable Diseases and Immunology, Walter Reed Army Institute of Research, Washington, D.C; the Department of Cancer Biology, Harvard School of Public Health, Boston; and Cambridge BioScience Corporation, Hopkinton, Massachusetts.
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▸Requests for reprints should be addressed to Donald S. Burke, COL, MC, Department of Virus Diseases, Walter Reed Army Institute of Research; Washington, DC 20307-5100.
- ©1987 American College of Physicians
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