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. 2004 Feb 17;101(9):3017–3022. doi: 10.1073/pnas.0308677101

Table 3. Cell-associated viral load and detection of vaccine and challenge forms of SIV by PCR 14-15 days after challenge.

SIVΔnef-vaccinated monkeys
Control nonvaccinated monkeys
10138 10140 11112 11118 10685 10686 10931 10932
PBMC C 64(nd) 2(C) 8,192 512 128(C) 128(C)
Palatine tonsil 16(V) 4,096(V/C) 32(V/C) 32(V/C) 8,192(C) 4,096(C) 512 32
Spleen 0.33(V) 4,096(V) 8(V) 4(V) 8,192 8,192 2,048(C) 256
LN axillary 4(V/C) 512(V/C) 8(V) 8(V) 4,096 8,192 8192 1,024
LN mesenteric 1,024(V/C) 4(C) 4,096 8,192 4096 8,192
LN submandibular 4(V) 1,024(V/C) 4(V) 32(V/C) 1,024 8,192 256 512
LN retropharyngeal 0.33(V) 1,024(V/C) 4(C) 16(nd) 4,096 8,192 4096 512
Thymus 0.33(V/C) 0.33(C) NA 64 1,024 1,024

Cell-associated viral load expressed as infectious units per 106 mononuclear cells. Characterization of reisolates by PCR are shown in parentheses.—, virus isolation negative; V, vaccine virus; C, challenge virus; nd, not done; NA, reisolate not available due to bacterial contamination. In the control animals, we performed PCR on only one to two reisolates per monkey, as indicated, to verify the presence of wild-type challenge virus.