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Immune complex transfer enzyme immunoassay for antibody IgG to HIV-1 gp41 antigen using synthetic peptides as antigens

โœ Scribed by Seiichi Hashida; Setsuko Ishikawa; Kazuya Hashinaka; Ichiro Nishikata; Shinichi Oka; Eiji Ishikawa


Publisher
John Wiley and Sons
Year
1998
Tongue
English
Weight
98 KB
Volume
12
Category
Article
ISSN
0887-8013

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โœฆ Synopsis


The immune complex transfer enzyme immunoassay for antibody IgG to HIV-1 gp41 antigen was developed using two synthetic peptides. An aliquot (10 ยตl) of serum samples from HIV-1 seropositive subjects was incubated simultaneously with 2,4-dinitrophenylbovine serum albumin-synthetic HIV-1 gp41 peptide conjugates and synthetic HIV-1 gp41 peptide-ฮฒ-D-galactosidase conjugates and subsequently with colored polystyrene beads coated with affinity-purified (anti-2,4dinitrophenyl group) IgG to trap the immune complexes formed comprising the three components. After washing, the colored polystyrene beads were incubated with white polystyrene beads coated with affinity-purified (anti-human IgG ฮณ-chain) IgG in the presence of eN-2,4-dinitrophenyl-L-lysine to transfer the immune complexes to the white polystyrene beads. ฮฒ-D-Galactosidase activity bound to the white polystyrene beads was assayed by fluorometry. The formation, trapping and transferring of the immune complexes were completed within 0.5, 0.5 and 1.5 hr, respectively. Since each peptide appeared to react with its own specific antibody IgG, serum samples were tested by the equimolar combination of the two peptides. The lowest signals (fluorescence intensities for bound ฮฒ-D-galactosidase activity) for serum samples from HIV-1 asymptomatic carriers, patients with AIDS-related complex and patients with AIDS were 1490-, 2210-and 1460-fold, respectively, higher than the highest signal for serum samples from HIV-1 seronegative subjects. In five seroconversion serum panels, antibody IgG to HIV-1 gp41 antigen was detected as early as antibodies to HIV-1 detected by three currently commercially available methods.


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