Fig. 7.
Fig. 7. CD4+CD25+ cells from umbilical cord blood of normal-term infants are phenotypically similar to those from adult peripheral blood. / (A) Cord blood mononuclear cells were isolated and stained with anti-CD4–QR, anti-CD25− PE, and FITC-conjugated monoclonal antibodies as indicated (middle panel). The dot plots were gated on CD4+ lymphocytes as shown in the top panel. Peripheral mononuclear cells from cord blood were stained with anti-CD4–QR, anti-CD25− FITC, and anti–CTLA-4–PE (thin solid lines) or isotype-matched control (thick solid lines). The histogram plot was gated on CD4+CD25+ or CD4+CD25− lymphocytes (bottom panel). (B) Limiting dilution analyses using CD4+ (♦) or CD4+CD25− (■) cells as responder cells. Serial dilutions of responder cells were cocultured with allogeneic irradiated PBMCs (5 × 104) for 5 days. Control wells contained stimulator cells only.

CD4+CD25+ cells from umbilical cord blood of normal-term infants are phenotypically similar to those from adult peripheral blood.

(A) Cord blood mononuclear cells were isolated and stained with anti-CD4–QR, anti-CD25 PE, and FITC-conjugated monoclonal antibodies as indicated (middle panel). The dot plots were gated on CD4+ lymphocytes as shown in the top panel. Peripheral mononuclear cells from cord blood were stained with anti-CD4–QR, anti-CD25 FITC, and anti–CTLA-4–PE (thin solid lines) or isotype-matched control (thick solid lines). The histogram plot was gated on CD4+CD25+ or CD4+CD25 lymphocytes (bottom panel). (B) Limiting dilution analyses using CD4+ (♦) or CD4+CD25 (■) cells as responder cells. Serial dilutions of responder cells were cocultured with allogeneic irradiated PBMCs (5 × 104) for 5 days. Control wells contained stimulator cells only.

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