Effect of T-Cell Clones on Autologous Hematopoietic Progenitor Cell Growth
Cells Plated for Progenitor Cell Assay . | T-Cell Clone Added . | Preincubation . | CFU-GM . | BFU-E . |
---|---|---|---|---|
Experiment 1 | ||||
Freshly obtained CD34+ cells | — | − | 232 ± 17 | 192 ± 12 |
NT4.2 | − | 194 ± 25 | 152 ± 16 | |
NT4.2 | + | 201 ± 12 | 144 ± 16 | |
NT27 | + | 194 ± 19 | 166 ± 11 | |
Cultured CD34+ cells | — | − | 98 ± 13 | 7 ± 2 |
NT4.2 | − | 74 ± 6 | 6 ± 2 | |
NT4.2 | + | 2 ± 1 | 1 ± 1 | |
NT27 | + | 78 ± 4 | 8 ± 2 | |
Experiment 2 | ||||
Cryopreserved-thawed CD34+ cells* | — | − | 92 ± 6 | 40 ± 3 |
NT4.2 | − | 80 ± 5 | 34 ± 3 | |
NT4.2 | + | 81 ± 5 | 31 ± 5 | |
Cultured CD34+ cells | — | − | 78 ± 6 | 19 ± 3 |
NT4.2 | − | 70 ± 2 | 15 ± 1 | |
NT4.2 | + | 3 ± 1 | 0 | |
NT4.2 + DR MoAb† | + | 40 ± 7 | 6 ± 1 |
Cells Plated for Progenitor Cell Assay . | T-Cell Clone Added . | Preincubation . | CFU-GM . | BFU-E . |
---|---|---|---|---|
Experiment 1 | ||||
Freshly obtained CD34+ cells | — | − | 232 ± 17 | 192 ± 12 |
NT4.2 | − | 194 ± 25 | 152 ± 16 | |
NT4.2 | + | 201 ± 12 | 144 ± 16 | |
NT27 | + | 194 ± 19 | 166 ± 11 | |
Cultured CD34+ cells | — | − | 98 ± 13 | 7 ± 2 |
NT4.2 | − | 74 ± 6 | 6 ± 2 | |
NT4.2 | + | 2 ± 1 | 1 ± 1 | |
NT27 | + | 78 ± 4 | 8 ± 2 | |
Experiment 2 | ||||
Cryopreserved-thawed CD34+ cells* | — | − | 92 ± 6 | 40 ± 3 |
NT4.2 | − | 80 ± 5 | 34 ± 3 | |
NT4.2 | + | 81 ± 5 | 31 ± 5 | |
Cultured CD34+ cells | — | − | 78 ± 6 | 19 ± 3 |
NT4.2 | − | 70 ± 2 | 15 ± 1 | |
NT4.2 | + | 3 ± 1 | 0 | |
NT4.2 + DR MoAb† | + | 40 ± 7 | 6 ± 1 |
A total of 3 × 103 freshly isolated CD34+ cells or CD34+ cells cultured in the presence of colony-stimulating factors were incubated in medium alone or with 3 × 104 cloned T cells for 4 hours (preincubation +) and then mixed with methylcellulose medium supplemented with growth factors. Some CD34+ cells were mixed with cloned T cells just before addition of the methylcellulose medium (preincubation −). Data are expressed as mean ± standard error of duplicate cultures.
An aliquot of autologous CD34+ cells that had been cryopreserved was used in Experiment 2.
Anti–HLA-DR MoAb, ascites 1/100, was added to the culture of CD34+ cells with NT4.2.