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. 1998 Jun;72(6):5231–5238. doi: 10.1128/jvi.72.6.5231-5238.1998

TABLE 7.

Levels of HIV gag mRNA/105 viable cells in TH1 and TH2 clones after HIV-1 infection

Clonea Type Antigen specificity HIV gag RNA (mol/105 viable cells)b
Day 7 Day 14
H1.19 TH1 TTx 7,300 108,000
H1.19 TH1 PMA–anti-CD3 8,400 205,000
H1.15 TH1 TTx 12,700 231,000
H1.18 TH1 TTx 9,700 196,000
H2.29 TH2 TTx 4,600 87,000
H2.33 TH2 TTx 5,300 95,000
H2.25 TH2 TTx 3,800 79,000
a

Derivation, antigen activation, and HIVIIIB infection of T-cell clones were performed as described in Materials and Methods. The H1.19 clone was not previously described. 

b

Construction and use of an RNA standard and RT-PCR analysis are described in Materials and Methods. For quantitation of number of HIV gag mRNA molecules, the gel was scanned on a PhosphorImager (Molecular Dynamics), using ImageQuant and Microsoft Excel programs, in comparison to a standard curve on each gel. Viable cells were separated by Ficoll-Hypaque density centrifugation.