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 |
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.
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.