Table 2.

Effect of T-Cell Clones on Autologous Hematopoietic Progenitor Cell Growth

Cells Plated for Progenitor Cell AssayT-Cell Clone AddedPreincubationCFU-GMBFU-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 
 NT4.2 + DR MoAb 40 ± 7 6 ± 1 
Cells Plated for Progenitor Cell AssayT-Cell Clone AddedPreincubationCFU-GMBFU-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 
 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.

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