Fig. 2.
Fig. 2. Virus DNA in PBMCs after autologous transfusion. / Semiquantitative DNA-PCR was performed from fresh PBMCs. DNA from cell mixtures was used as control. For this purpose, herpesvirus saimiri–transformed human T cells were mixed with PHA/IL-2–stimulated human T cells at ratios of 0/106, 1/106, 10/106, 102/106, and 103/106. The time points of the PBMC preparations after the first autologous transfusion are marked for day 2 (d2), day 4 (d4), and week 1 (w1) to week 16 (w16). PCR for 2 different virus genes, stpC and vIL-17, is shown for monkey Mm7067.

Virus DNA in PBMCs after autologous transfusion.

Semiquantitative DNA-PCR was performed from fresh PBMCs. DNA from cell mixtures was used as control. For this purpose, herpesvirus saimiri–transformed human T cells were mixed with PHA/IL-2–stimulated human T cells at ratios of 0/106, 1/106, 10/106, 102/106, and 103/106. The time points of the PBMC preparations after the first autologous transfusion are marked for day 2 (d2), day 4 (d4), and week 1 (w1) to week 16 (w16). PCR for 2 different virus genes, stpC and vIL-17, is shown for monkey Mm7067.

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