V. Weisbach et al., The influence of automated plateletpheresis on systemic levels of hematopoietic growth factors, TRANSFUSION, 39(8), 1999, pp. 889-894
BACKGROUND: Megakaryocytopoiesis and platelet production are regulated by s
everal hematopoietic growth factors. The present study focuses on the effec
ts of automated plateletpheresis on systemic levels of different hematopoie
tic growth factors.
STUDY DESIGN AND METHODS: Platelet count, mean platelet volume, and serum l
evels of thrombopoietin, erythropoietin, interleukin-1 beta, interleukin-6,
and stem cell factor in 21 healthy donors were measured before platelet co
llection, after the first half of the apheresis procedure, at the end of ap
heresis, and on Days 1, 2, and 7 thereafter.
RESULTS: Thrombopoietin levels (initial level: 49.5 +/- 25.5 pg/mL) showed
a significant increase between measurements taken at the end of apheresis a
nd Day 1 (56.9 +/- 26.7 pg/mL; p = 0.01). There was a highly significant de
crease in stem cell factor levels during apheresis (p < 0.0005), reaching p
reapheresis values (1679 +/- 210 pg/mL) on Day 1. A highly significant incr
ease in erythropoietin levels (initial level: 7.5 +/- 4.0 U/L) was seen aft
er apheresis (p < 0.0005 on Days 1 and 2).The level remained significantly
elevated until Day 7 (p = 0.004). Interleukin-1 beta and interieukin-6 leve
ls (before donation: 1.4 +/- 1.8 pg/mL and 1.1 +/- 0.7 pg/mL, respectively)
did hot change during the observation period. Thrombopoietin levels correl
ated consistently and inversely with stem cell factor levels after apheresi
s (Day 1, r = -0.46, p = 0.035; Day 2, r = -0.50, p = 0.02; Day 7, r = -0.5
0, p = 0.02).
CONCLUSION: The data show a coordinated response of the hematopoietic syste
m to platelet loss. It is suggested that the decrease in serum stem cell fa
ctor levels during apheresis reflects the consumption of stem cell factor b
y early hematopoietic progenitors that expand to initiate early megakaryocy
topoiesis. The temporary increase in thrombopoietin is the result of platel
et loss and serves as a stimulus for subsequent thrombopoiesis. The pronoun
ced elevation of erythropoietin after apheresis suggests a role for this pr
imarily erythropoietic cytokine in thrombopoiesis, too.