Ishikawa S, Hashida S, Hashinaka K, Adachi A, Oka S, Ishikawa E
Department of Biochemistry, Miyazaki Medical College, Kiyotake, Japan.
J Clin Lab Anal. 1998;12(4):227-37. doi: 10.1002/(sici)1098-2825(1998)12:4<227::aid-jcla7>3.0.co;2-4.
In order to perform the immune complex transfer enzyme immunoassays for HIV-1 p24 antigen and antibody IgGs to HIV-1 p17, reverse transcriptase and gp41 antigens as rapidly as possible, methods for rapid formation of the immune complexes on solid phase are described. HIV-1 p24 antigen was reacted with monoclonal anti-p24 Fab'-beta-D-galactosidase conjugate at a high concentration and subsequently with polystyrene beads coated successively with affinity-purified (anti-2,4-dinitrophenyl group) IgG and 2,4-dinitrophenyl-biotinyl bovine serum albumin-affinity-purified anti-p24 Fab' conjugate. Antibody IgGs to HIV-1 were reacted with polystyrene beads coated successively with affinity-purified (anti-2,4-dinitrophenyl group) IgG and 2,4-dinitrophenyl-HIV-1 antigen conjugates and subsequently with HIV-1 antigen-beta-D-galactosidase conjugates. The periods of time used for the formation of the immune complexes comprising the three components on the polystyrene beads (15-30 min) were much shorter than those used in the previous immune complex transfer enzyme immunoassays (90-300 min), and the sensitivities of the present and previous immune complex transfer enzyme immunoassays were similar. The detection limit of the HIV-1 p24 antigen by the present and previous methods were similar (3 to 10 zmol/assay).
为了尽快进行针对HIV-1 p24抗原以及针对HIV-1 p17、逆转录酶和gp41抗原的抗体IgG的免疫复合物转移酶免疫测定,本文描述了在固相中快速形成免疫复合物的方法。HIV-1 p24抗原与高浓度的单克隆抗-p24 Fab'-β-D-半乳糖苷酶缀合物反应,随后与依次包被有亲和纯化的(抗-2,4-二硝基苯基)IgG和2,4-二硝基苯基-生物素化牛血清白蛋白-亲和纯化的抗-p24 Fab'缀合物的聚苯乙烯珠反应。针对HIV-1的抗体IgG与依次包被有亲和纯化的(抗-2,4-二硝基苯基)IgG和2,4-二硝基苯基-HIV-1抗原缀合物的聚苯乙烯珠反应,随后与HIV-1抗原-β-D-半乳糖苷酶缀合物反应。在聚苯乙烯珠上形成包含三种成分的免疫复合物所用的时间(15 - 30分钟)比先前的免疫复合物转移酶免疫测定所用的时间(90 - 300分钟)短得多,并且当前和先前的免疫复合物转移酶免疫测定的灵敏度相似。通过当前方法和先前方法检测HIV-1 p24抗原的检测限相似(3至10 zmol/测定)。