Table 2.

Secondary Colony Formation in the Course of BMLTC Initiated With Purified CD34+ Cells Exposed to HIV-1 and HIV-2

Time of BMLTCCD34+CD38+ CellsCD34+CD38 Cells
1 wk3 wk LTCIC 1 wk 3 wk LTCIC
gp120  96  106 97  104  98  106  
HIV-1 Bal  94  102  102 103  105  100  
HIV-1 Bal mock (H*)  102  98  108 109  101  97  
HIV-1 Bal mock (R*)  98  100  102 106  100  104  
HIV-1 RF  97  98  107  110 102  98  
HIV-2 Rod  105  96  110  97  102 108  
HIV-2 Rod mock (R*)  101  98  96  113  94 95  
Sup (LPS)  106  98  109  99  106 98 
Time of BMLTCCD34+CD38+ CellsCD34+CD38 Cells
1 wk3 wk LTCIC 1 wk 3 wk LTCIC
gp120  96  106 97  104  98  106  
HIV-1 Bal  94  102  102 103  105  100  
HIV-1 Bal mock (H*)  102  98  108 109  101  97  
HIV-1 Bal mock (R*)  98  100  102 106  100  104  
HIV-1 RF  97  98  107  110 102  98  
HIV-2 Rod  105  96  110  97  102 108  
HIV-2 Rod mock (R*)  101  98  96  113  94 95  
Sup (LPS)  106  98  109  99  106 98 

CFC are expressed as percentage of the mean values of control cultures for each time point (SD < 9%). All BMLTC were performed in duplicate and each culture was assessed in triplicate methylcellulose cultures to determine the number of CFC. The number of colonies in controls was 2,980 ± 270, 1,040 ± 110, 158 ± 18, 50 ± 6, and 24 ± 5 for weeks 1, 2, 3, 4, and 5, per 105CD34+ cells, respectively. The control colony numbers for CD34+CD38 sorted cells were 820 ± 58, 510 ± 58, 234 ± 18, 148 ± 11, 92 ± 10 for 1 to 5 weeks per 104 cells. Heat inactivated (H*) and irradiated virus stocks (R*) were used as indicated.

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