Identification of complement activators and elucidation of the fate of complement activation products during extracorporeal plasma purification therapy
Jem. Fadul et al., Identification of complement activators and elucidation of the fate of complement activation products during extracorporeal plasma purification therapy, J CLIN APH, 13(4), 1998, pp. 167-173
It has been known for many years that the complement system is activated du
ring extracorporeal plasma purification (ECCP) therapy. In a previous study
, we showed that high concentrations of complement activation products (CAP
s) are returned to the patient during immunoadsorption treatment. In the pr
esent study, we investigated the question of where complement activation ta
kes place with different forms of ECPP equipments as well as the fate of th
e CAPs. Eleven patients (8 men and 3 women), mean age 52 +/- 18 years, were
included in the study. They were treated either with plasmapheresis (PP),
immunoadsorption, bilirubin adsorption, or low density lipoprotein (LDL) ap
heresis. It was found that during all ECPP treatments and after the plasma
separation filter, the plasma concentrations of CAPs were increased, and th
at high concentrations of CAPs were returned to the patients, except with P
P. The plasma levels of individual CAPs varied between different types of E
CPP. These variations were due to several factors: (1) complement activatio
n (CA) on the plasma separator and a secondary device, e.g., column or memb
rane; (2) adsorption of specific CAPs to separation columns; and (3) reduct
ion of CAPs due to separation and waste. Since CAPs have inflammatory and i
mmunological effects, it is possible that high serum concentration of CAPs
in the treated patients may influence the clinical outcome of the treatment
. In conclusion, complement activation is a fact that should not be ignored
during performance of any form of an ECPP. It is the plasma separator that
plays a key role in the process of complement activation. Different ECPP t
reatments may have different effects regarding the levels of individual CAP
s. J. Clin. Apheresis 13:167-173, 1998. (C) 1998 Wiley-Liss,Inc.