Document 2739 DOCN M94A2739 TI p24 in serum from HIV-1 seropositives. DT 9412 AU Hashida S; Hashinaka K; Nishikata I; Oka S; Shimada K; Saitoh A; Shinagawa H; Takamizawa A; Ishikawa E; Department of Biochemistry, Medical College of Miyazaki, Japan. SO Int Conf AIDS. 1994 Aug 7-12;10(1):236 (abstract no. PB0374). Unique Identifier : AIDSLINE ICA10/94369836 AB OBJECTIVE: To test the positivity of p24 assayed by a new enzyme immunoassay (EIA) in sera from HIV-1 seropositives. METHOD: An ultrasensitive two-site enzyme immunoassay (two-site complex transfer enzyme immunoassay) was developed. The immune complex consisting of 2,4-dinitrophenyl (DNP)-biotinyl-bovine serum albumin-anti-p24 Fab', p24 and anti-p24 Fab'-beta-D-galactosidase (GAL) conjugate was trapped onto anti-DNP IgG-coated polystyrene balls (PS), eluted with DNP-L-lysine and transferred to streptavidin-coated PS. GAL activity bound to the last PS was assayed by fluorometry. RESULTS: The detection limit of p24 was 0.24 ng/l using 10 microliters of serum. p24 was detected in 50 out of 79 sera from seropositives (25 out of 50 sera from asymptomatic carriers (AC) and 25 out of 29 sera from advanced patients) and all negative in 100 sera from seronegatives. Thus, the sensitivity and specificity of the assay were 64% and 100%, respectively. Furthermore, after acid-treatment of serum, the sensitivity increased to 75% (68% even for AC) with no change in the specificity. DISCUSSION AND CONCLUSIONS: The sensitivity of the new assay was apparently superior to those of commercially available kits. The high positivity of p24 assayed by the method in sera may allow us to use p24 a useful surrogate marker. DE Human HIV Core Protein p24/*BLOOD HIV Seropositivity/CLASSIFICATION/*DIAGNOSIS/IMMUNOLOGY HIV-1/*IMMUNOLOGY *Immunoenzyme Techniques Predictive Value of Tests MEETING ABSTRACT SOURCE: National Library of Medicine. NOTICE: This material may be protected by Copyright Law (Title 17, U.S.Code).