Abstract |
With the introduction of combination therapy to the patients with Human Immunodeficiency Virus Type 1(HIV-1) infection, HIV-1 RNA levels in plasma have been reduced, frequently to less than limit of quantitation(400 copies/ml). To achieve enhanced sensitivity, a modified specimen preparation procedure that allows the quantitation of plasma HIV-1 RNA levels as low as 50 copies/ml was developed. Of 67 samples with less than 400 copies/ml of HIV-1 RNA by standard method, 39(58.2%) were not detected by the "ultrasensitive" method. Among 5 samples obtained from patients who were treated with 2 nucleoside reverse transcriptase inhibitors, 4 samples still had detectable copies of HIV-1 RNA. Those suggest that the ultrasensitive assay for HIV-1 RNA has advantage for clinical practice.
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Authors | Y Nishida, K Moriya, K Nagaizumi, H Inaba, K Amano, H Fukue, Y Yamamoto, M Arai, K Fukutake |
Journal | Rinsho byori. The Japanese journal of clinical pathology
(Rinsho Byori)
Vol. 48
Issue 3
Pg. 282-3
(Mar 2000)
ISSN: 0047-1860 [Print] Japan |
PMID | 10804838
(Publication Type: English Abstract, Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
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Topics |
- HIV Infections
(blood)
- HIV-1
(genetics, isolation & purification)
- Humans
- Methods
- RNA, Viral
(blood)
- Sensitivity and Specificity
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