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. Author manuscript; available in PMC: 2006 Jun 5.
Published in final edited form as: J Immunother. 2005;28(4):403–411. doi: 10.1097/01.cji.0000170363.22585.5a

TABLE 2.

Phenotypic Analysis of Pheresis Products After CD25 Depletion

Lymphocyte-Gated Cells
Donor %CD3+of Total % CD3+ % CD8+of CD3 % CD4+of CD3 % CD4+CD25+
1 Pre-separation 51 78 22 70 52
Post-CD25+ fraction 84 91 7 91 56
Post-CD25 fraction 45 75 36 55 <1
2 Pre-separation 55 77 65 33 61
Post-CD25+ fraction 83 88 16 82 67
Post-CD25 fraction 51 72 79 17 <1

Pre- and post-CD25 depletion donor 1 and 2 pheresis samples were blocked with normal mouse immunoglobulin before staining with mouse anti-CD3, CD4, CD8, or CD25 antibodies and viable cells selected through PI gating. For CD25 staining, primary biotin-labeled antibody staining was followed by secondary anti-biotin antibody staining. Values correspond to the percentage of positive events within the total cell population or lymphocyte-gated population as indicated.