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Protocol NUCB 2019. Participants underwent serial venipuncture for T cell subsets, plasma HIV RNA, and genotypic virology.
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note
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+ cell count was 194 cells per cubic millimeter.
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17
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15144357396
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note
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1/2 values, the mean pool sizes shown in Table 1, and the number of days of treatment. Because the FDC pool stores most virus produced, the simplest explanation for the earty rapid elimination of FDC-associated virus is that it is a result of treatment-induced reductions in MNC virus manufacture. Dividing the initial turnover per day in the FDC pool by the initial turnover per day of MNC thus gives an estimate of the number of copies of viral RNA per productively infected MNC.
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15144350489
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35S-labeled HIV RNA probe. After post-hybridization washes, nonspecific binding of antibodies was blocked by immersing the sections in 5% nonfat milk in phosphate-buffered saline (PBS) for 30 min. Sections were then treated with a 1:300 dilution of CD68 mAb (Dako, Carpinteria, CA) at 4°C overnight. After washing, slides were developed with a peroxidase-conjugated secondary antibody and diaminobenzidene substrate according the manufacturer's protocol (ABC Elite kit; Vector Labs, Burlingame, CA). The sections were then washed in PBS and 0.1 × PBS, dehydrated in ethanol containing 0.3 M ammonium acetate, and coated with nuclear track emulsion. After development, the slides were briefly counterstained in hematoxylin.
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note
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4 copies per gram of LT.
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15144355467
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note
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32P]deoxyadenosine triphosphate specific for sequences internal to the nesting primers (30-nucteotide oligomers: 5′-CATGGGTAAAAGTAGTAGAAGAGAAGGCTT-3′, 5′-GGGACATCAAGCAGCCATGCAAATGTTAAA-3′,5′- CCAAGGGGAAGTGACATAGCAGGAACTACT-3′).
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in preparation
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0002681215
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note
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We thank P. Dailey for technical assistance; C. O'Neill, T. Leonard, and G. Sedgewick for assistance with preparation of the manuscript and figures; and J. Leonard and G. Goodwin for clinical support. Supported by NIH grants Al 25017 and Al 28246.
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