Clin Chem. 1992 May;38(5):699-703. Unique Identifier : AIDSLINE
We developed an enzyme immunoassay (EIA) system to detect antibodies to
human T-lymphotropic virus type I (HTLV-I). This system uses chemically
synthesized oligopeptides to capture anti-HTLV-I antibodies in serum.
The two epitopes of HTLV-I proteins exhibiting the most specific
antigen-antibody reaction reside within amino acids 100-130 of p19, a
core protein encoded by gag, and amino acids 175-199 of gp46, an
envelope glycoprotein encoded by env. This new assay uses synthetic
peptides corresponding to these two regions modified by adding two
lysine residues at the amino terminal of each peptide to facilitate the
binding to the surface of the microtiter plate wells. We compared the
performance of our EIA with gelatin-particle-agglutination (PA) and
indirect-immunofluorescence (IF) assays, both of which use viral
proteins purified from virus-carrying cell cultures. Mass screening by
EIA with various synthetic peptides was more accurate than the current
confirmatory IF assay.
Agglutination Tests Comparative Study Fluorescent Antibody Technique
Gene Products, env/IMMUNOLOGY Gene Products, gag/IMMUNOLOGY Human
HTLV-I Antibodies/*BLOOD HTLV-I Antigens/IMMUNOLOGY *Immunoenzyme
Techniques JOURNAL ARTICLE