Fig. 2.
Fig. 2. Lymphocyte subsets and proliferation to mitogens before transplantation and after transplantation in SCID infants given stem cell transplants in the neonatal period. / (A-B) The mean (± SEM) numbers of T, B, and NK cells at birth (A) and at the latest posttransplantation evaluation (B) for surviving patients according to genotype. ▪, CD3+ T cells; ■, CD20+ B cells; ░, CD16+ NK cells. Normal range represents the 95% confidence interval for healthy infants at birth (A) or for healthy children at 6 years of age (B). (C) The mean (± SEM) counts per minute of3Hthymidine incorporation by proliferating PBMCs stimulated with PHA (▪), concanavalin A (■), and pokeweed (░) mitogens before transplantation and at the most recent evaluation compared with healthy controls.

Lymphocyte subsets and proliferation to mitogens before transplantation and after transplantation in SCID infants given stem cell transplants in the neonatal period.

(A-B) The mean (± SEM) numbers of T, B, and NK cells at birth (A) and at the latest posttransplantation evaluation (B) for surviving patients according to genotype. ▪, CD3+ T cells; ■, CD20+ B cells; ░, CD16+ NK cells. Normal range represents the 95% confidence interval for healthy infants at birth (A) or for healthy children at 6 years of age (B). (C) The mean (± SEM) counts per minute of3Hthymidine incorporation by proliferating PBMCs stimulated with PHA (▪), concanavalin A (■), and pokeweed (░) mitogens before transplantation and at the most recent evaluation compared with healthy controls.

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