Je. Talmadge et al., IMMUNOLOGICAL ATTRIBUTES OF CYTOKINE MOBILIZED PERIPHERAL-BLOOD STEM-CELLS AND RECOVERY FOLLOWING TRANSPLANTATION, Bone marrow transplantation, 17(1), 1996, pp. 101-109
The immunologic attributes of cytokine mobilized peripheral blood stem
cell (PSC) products (n = 52) and the resulting reconstitution of the
hematopoietic and immunologic system following autologous transplantat
ion were examined in a consecutive population of non-Hodgkin lymphoma
(NHL), or solid tumor patients at the University of Nebraska Medical C
enter. Granulocyte-monocyte colony stimulating factor (GM-CSF)-mobiliz
ed PSC products had a high frequency of monocytes (31%) and bands (15%
) as compared to normal peripheral blood (PB) cells. The phenotypic an
alysis of the mobilized PSC product revealed that they had normal leve
ls of CD4(+) cells, an increased frequency of CD8(+) cells and a corre
sponding decrease in the CD4(+):CD8(+) cell ratio as compared to the p
eripheral blood leukocytes (PBL) of normal individuals. PSC products a
lso had an increase in CD34(+) cells as compared to PB. Natural killer
(NK) and T cell activity in the PSC products were also lower than tha
t observed in PB. post-transplantation there was an accelerated recons
titution of NK-cell function in the PB as compared to T cell function
(PHA (phytohemagglutinin) mitogenesis) which did not return to normal
by day 100 post-transplantation. We also report for the first time hig
h levels of an irradiation resistant suppressor cell activity in the P
SC product and in the PB post-transplantation. There was also a concom
itant increase in CD4(-), CD8(-), TCR alpha/beta(+) cells (phenotypic
homolog of 'natural suppressor' (NS) cells) in the PB post-transplanta
tion. The number of months of prior chemotherapy correlated with PHA r
esponse but the NS activity and frequency of CD4(-), CD8(-) and TCR al
pha/beta(+) cells did not. Further, cytokine mobilization and apheresi
s appears to contribute to the loss of PHA responsiveness and the incr
eased levels of suppressor cell activity.