Delord B, Ottmann M, Schrive M H, Ragnaud J M, Seigneurin J M, Fleury H J
Laboratoire de Virologie, Université de Bordeaux II, France.
Mol Cell Probes. 1992 Jun;6(3):215-21. doi: 10.1016/0890-8508(92)90019-t.
The objective of the present study was to compare the data of in situ hybridization (ISH), RNA polymerase chain reaction (PCR/RNA) and p24 core antigen (p24 Ag) enzyme immunoassay (EIA) for the detection of HIV-1 expression in peripheral blood mononuclear cells (PBMCs) and in plasma of infected patients at various CDC stages. PBMCs of 24 patients mostly of CDC stage II were obtained from heparinized blood samples, cytocentrifuged and hybridized with a (35S) labelled single-stranded RNA probe specific for gag-pol of LAVBru HIV-1 allowing the detection of genomic and/or messenger RNA. The corresponding plasma samples were used for the determination of p24 Ag by EIA and detection of HIV-1 genomic RNA by RT-PCR using specific primers in the LTR, gag and env regions. Whereas p24 was detected in only six out of 24 patients, both ISH and PCR/RNA enabled the detection of viral RNAs in more than 60% of the patients; cumulation of positive results of ISH and RT-PCR showed that 100% of patients at stage IV and 83% of patients at stages II/III have molecular signs of HIV expression therefore indicating that transcription of the provirus is a highly frequent event, even in the early stages of the disease, and, pleading for undertaking a very early antiviral chemotherapy.
本研究的目的是比较原位杂交(ISH)、RNA聚合酶链反应(PCR/RNA)和p24核心抗原(p24 Ag)酶免疫测定(EIA)的数据,以检测不同疾病控制中心(CDC)阶段感染患者外周血单核细胞(PBMC)和血浆中HIV-1的表达情况。从24例大多处于CDC II期的患者的肝素化血样中获取PBMC,经细胞离心涂片后,与针对LAVBru HIV-1的gag-pol的(35S)标记单链RNA探针杂交,以检测基因组RNA和/或信使RNA。相应的血浆样本用于通过EIA测定p24 Ag,并使用LTR、gag和env区域的特异性引物通过逆转录聚合酶链反应(RT-PCR)检测HIV-1基因组RNA。在24例患者中,只有6例检测到p24,而ISH和PCR/RNA均能在60%以上的患者中检测到病毒RNA;ISH和RT-PCR阳性结果的累积显示,IV期患者中有100%以及II/III期患者中有83%具有HIV表达的分子迹象,因此表明即使在疾病早期,前病毒转录也是一个非常常见的事件,这为尽早进行抗病毒化疗提供了依据。