Table 1.

Characteristics for 18 HIV-1—infected patients



CD4 cells/mm3

CD8 cells/mm3




DCs in PBMCs, %

No. DCs/mL blood
Patient no.
HIV VL copies/mL
HAART
ACTG stage
MDC
PDC
MDC
PDC
Patients with KS           
    1   576   1146   < 50   3TC, aba, lop, ten   T0I0   0.33   0.08   2438   600  
    2   484   1449   < 50   3TC, ind, D4T   T0I0   0.23   0.01   2901   139  
    3   392   756   < 50   rit, ind, AZT, 3TC   T0I0   0.21   0.01   1608   112  
    4   363   663   < 50   3TC, aba, nev   T0I0   0.31   0.04   1248   164  
    5   147   705   < 50   comb, nev   T1I1   0.28   0.03   1175   137  
    6   169   406   < 50   comb, efa   T0I1   0.24   0.05   1673   357  
    7   104   317   374 490   AZT, 3TC, efa   T1I0   0.15   0.01   980   67  
    8   115   1273   450 614   AZT, 3TC, efa   T1I0   0.17   0.02   717   100  
    9   128   251   5 311   Trizivir, efa   T1I0   0.3   0.02   602   42  
    10   132   617   < 50   lop, ten, DDI   T1I0   0.16   0.07   80   34  
    11   28   329   < 50   comb, efa   T1I0   0.16   0.02   161   20  
    12   52   188   < 50   Trizivir, efa   T1I0   —    —   —  
Patients without KS           
    13   526   930   < 50   Trizivir   NA   0.22   0.19   1980   1760  
    14   364   369   < 50   comb, efa   NA   0.26   0.25   1813   1729  
    15   168   274   < 50   comb, rit, ind   NA   0.29   0.27   1698   1581  
    16   126   758   176 555   D4T, 3TC, aba   NA   0.28   0.19   1321   882  
    17   148   236   3 658   comb, efa   NA   0.29   0.25   488   417  
    18
 
64
 
197
 
< 50
 
DDI, 3TC, efa
 
NA
 
0.18
 
0.22
 
175
 
221
 


CD4 cells/mm3

CD8 cells/mm3




DCs in PBMCs, %

No. DCs/mL blood
Patient no.
HIV VL copies/mL
HAART
ACTG stage
MDC
PDC
MDC
PDC
Patients with KS           
    1   576   1146   < 50   3TC, aba, lop, ten   T0I0   0.33   0.08   2438   600  
    2   484   1449   < 50   3TC, ind, D4T   T0I0   0.23   0.01   2901   139  
    3   392   756   < 50   rit, ind, AZT, 3TC   T0I0   0.21   0.01   1608   112  
    4   363   663   < 50   3TC, aba, nev   T0I0   0.31   0.04   1248   164  
    5   147   705   < 50   comb, nev   T1I1   0.28   0.03   1175   137  
    6   169   406   < 50   comb, efa   T0I1   0.24   0.05   1673   357  
    7   104   317   374 490   AZT, 3TC, efa   T1I0   0.15   0.01   980   67  
    8   115   1273   450 614   AZT, 3TC, efa   T1I0   0.17   0.02   717   100  
    9   128   251   5 311   Trizivir, efa   T1I0   0.3   0.02   602   42  
    10   132   617   < 50   lop, ten, DDI   T1I0   0.16   0.07   80   34  
    11   28   329   < 50   comb, efa   T1I0   0.16   0.02   161   20  
    12   52   188   < 50   Trizivir, efa   T1I0   —    —   —  
Patients without KS           
    13   526   930   < 50   Trizivir   NA   0.22   0.19   1980   1760  
    14   364   369   < 50   comb, efa   NA   0.26   0.25   1813   1729  
    15   168   274   < 50   comb, rit, ind   NA   0.29   0.27   1698   1581  
    16   126   758   176 555   D4T, 3TC, aba   NA   0.28   0.19   1321   882  
    17   148   236   3 658   comb, efa   NA   0.29   0.25   488   417  
    18
 
64
 
197
 
< 50
 
DDI, 3TC, efa
 
NA
 
0.18
 
0.22
 
175
 
221
 

Twelve patients had histologically confirmed active KS; 6 HIV-1—infected patients were matched to these for CD4 count (within 50 cells/mm3) and HIV-1 RNA viral load (within 0.5 Log10) such that patients 1 and 2 (KS negative) were matched to patient 13 (KS positive), patients 3 and 4 were matched to patient 14, and so on. All patients were male, aged 25 to 40 years. The 6 patients without KS were confirmed as KSHV negative by PCR to 2 sections of the unique KSHV gene K1. The percentage and numbers of myeloid (CD11c+) and plasmacytoid (CD11c-) DCs are shown. Antiretrovirals include abacavir (aba), combivir (comb), efavirenz (efa), indinivir (ind), lopinivir (lop), nevirapine (nev), and ritonavir (rit). Median length of time on HAART was 3 years (range, 1-7 years). There were no statistically significant differences between the 2 groups for the median length of time on HAART, number of previous regimens, or CD8 counts (none of these criteria were included in the matching of KS-positive to -negative patients). DC subsets were not counted for 1 patient with KS. ACTG indicates AIDS Clinical Trials Group Oncology Committee,42  where (briefly) tumor status (0 indicates cutaneous only; 1, more than cutaneous disease) and immunologic status (0 indicates a CD4 count < 150; 1, CD4 count > 150 cells/mm3) are used to stage KS; NA indicates not applicable.

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