逆转录酶
病毒学
核糖核酸
外周血单个核细胞
聚合酶链反应
RNA提取
逆转录聚合酶链式反应
病毒
医学
实时聚合酶链反应
抗原
病毒性疾病
人类免疫缺陷病毒(HIV)
病毒载量
DNA
生物
免疫学
基因表达
基因
体外
生物化学
遗传学
作者
Clyde E. Hart,Thomas J. Spira,Jennifer Moore,John J. Sninsky,Gerald Schochetman,Alan R. Lifson,J C Galphin,Chin-Yih Ou
出处
期刊:The Lancet
[Elsevier]
日期:1988-09-01
卷期号:332 (8611): 596-599
被引量:149
标识
DOI:10.1016/s0140-6736(88)90639-3
摘要
The polymerase chain reaction (PCR) and reverse transcription were used to assess human immunodeficiency virus type 1 (HIV1) RNA expression in peripheral blood mononuclear cell samples from seropositive subjects. HIV RNA was detected from seropositive subjects who had no symptoms, lymphadenopathy syndrome, and acquired immunodeficiency syndrome. DNA PCR of the samples used for RNA extraction showed that seventeen of eighteen (94%) contained HIV proviral DNA. Eleven (65%) of the seventeen DNA-positive samples were also positive for HIV RNA, including samples from four patients undergoing antiviral drug treatment. Serum HIV antigen assays detected only six (32%) of the nineteen PCR-positive samples. Owing to the speed and high sensitivity of PCR for HIV detection, this technique will be suitable for monitoring antiviral therapy and the virus load of people with HIV infections.
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