Table 1.

HTLV-I replication in unfractionated PBMCs, CD8 PBMCs, and CD8 PBMCs reconstituted with autologous or allogeneic CD8+ T cells

Carrierp19 Ag level in culture supernatant (pg/mL)
Unfract PBMCsCD8PBMCsCD8 PBMCs plus*
auto CD8+ cellsallo CD8+ cells
(9:1)(4:1)(9:1)(4:1)
47 212 115  (46%) 25  (88%) 180  (15%) 77  (64%) 
36 465 190  (59%) 28  (94%) 358  (23%) 228  (51%)  
52 1120 512  (54%) 60  (95%) 2540  (—) 602  (46%)  
<25 240 152  (37%) 35  (85%) 140  (42%) 70  (71%) 
207 526 529  (—) 272  (48%) 393  (25%) 312  (41%)  
91 493 480  (3%) 111  (78%) 530  (—) 242  (51%) 
Carrierp19 Ag level in culture supernatant (pg/mL)
Unfract PBMCsCD8PBMCsCD8 PBMCs plus*
auto CD8+ cellsallo CD8+ cells
(9:1)(4:1)(9:1)(4:1)
47 212 115  (46%) 25  (88%) 180  (15%) 77  (64%) 
36 465 190  (59%) 28  (94%) 358  (23%) 228  (51%)  
52 1120 512  (54%) 60  (95%) 2540  (—) 602  (46%)  
<25 240 152  (37%) 35  (85%) 140  (42%) 70  (71%) 
207 526 529  (—) 272  (48%) 393  (25%) 312  (41%)  
91 493 480  (3%) 111  (78%) 530  (—) 242  (51%) 

HTLV-I = human T-cell lymphotropic virus type I; PBMCs = peripheral blood mononuclear cells; unfract = unfractionated. PBMCs were obtained from 3 pairs of HTLV-I carriers (1–6). Three million unfractionated PBMCs or CD8 PBMCs were propagated in RPMI 1640 medium supplemented with 10% fetal bovine serum. Cell-free culture supernatants were collected on day 7 of culture, and p19 levels were determined by ELISA.

*

Where indicated, CD8 PBMCs were reconstituted with autologous or allogeneic CD8+ T cells at the indicated ratio.

Allogeneic cultures were performed between carriers 1 and 2, carriers 3 and 4, and carriers 5 and 6.

Percentage suppression is expressed as: 100-(p19 Ag level of CD8 PBMC reconstituted with CD8+ T cells/p19 Ag level of CD8 PBMC alone).

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