Healey D S, Jowett J B, Beaton F, Maskill W J, Gust I D
National HIV Reference Laboratory, Fairfield Hospital for Communicable Diseases, Victoria, Australia.
J Virol Methods. 1987 Sep;17(3-4):237-45. doi: 10.1016/0166-0934(87)90134-0.
An enzyme immunoassay (EIA) was developed for detection of human immunodeficiency virus antigen (HIV Ag) in tissue culture supernatants. The assay was found to be specific for HIV and cheaper, easier to perform and more sensitive than the generally used reverse transcriptase (RT) assay. Cultures of peripheral blood leucocytes (PBL) from 106 patients with acquired immune deficiency syndrome (AIDS), AIDS related complex (ARC), healthy anti-HIV positive subjects and healthy anti-HIV negative subjects were held for 35 days and the supernatant fluid tested at regular intervals by EIA and RT. Of these 106 cultures, the presence of HIV was detected by EIA in 27 and by RT in 21. While six cultures were positive by EIA alone, none were positive by RT alone; the specificity of the results in the six EIA positive RT negative cultures was confirmed by subculture. In the 21 cultures in which HIV was detected by both techniques, the EIA became positive first on 10 occasions; in the remaining cultures both tests became positive at the same time. The HIV Ag assay reduces the time taken to process specimens and thus increases the efficiency and reduces the cost of isolation procedures.
开发了一种酶免疫测定法(EIA),用于检测组织培养上清液中的人类免疫缺陷病毒抗原(HIV Ag)。结果发现该测定法对HIV具有特异性,且比常用的逆转录酶(RT)测定法更便宜、更易于操作且更灵敏。对106例获得性免疫缺陷综合征(AIDS)患者、艾滋病相关综合征(ARC)患者、健康的抗HIV阳性受试者和健康的抗HIV阴性受试者的外周血白细胞(PBL)培养物进行了35天的培养,并定期通过EIA和RT检测上清液。在这106份培养物中,通过EIA检测到27份存在HIV,通过RT检测到21份。虽然有6份培养物仅EIA呈阳性,但没有一份仅RT呈阳性;通过传代培养证实了6份EIA阳性而RT阴性培养物结果的特异性。在两种技术均检测到HIV的21份培养物中,EIA有10次首先呈阳性;在其余培养物中,两种检测同时呈阳性。HIV Ag测定法减少了处理标本所需的时间,从而提高了效率并降低了分离程序的成本。