CYCLOSPORINE INHIBITION OF LEUKOCYTE CALCINEURIN IS MUCH LESS IN WHOLE-BLOOD THAN IN CULTURE-MEDIUM

Citation
Td. Batiuk et al., CYCLOSPORINE INHIBITION OF LEUKOCYTE CALCINEURIN IS MUCH LESS IN WHOLE-BLOOD THAN IN CULTURE-MEDIUM, Transplantation, 61(1), 1996, pp. 158-161
Citations number
15
Categorie Soggetti
Immunology,Surgery,Transplantation
Journal title
ISSN journal
00411337
Volume
61
Issue
1
Year of publication
1996
Pages
158 - 161
Database
ISI
SICI code
0041-1337(1996)61:1<158:CIOLCI>2.0.ZU;2-E
Abstract
Recent reports have shown that cyclosporine (CsA)-treated patients hav e abundant calcineurin phosphatase (CN) activity in vivo despite CsA b lood concentrations that would be completely inhibitory in vitro. We s ought to determine whether this disparity was a result of altered dist ribution of CsA in culture medium (CM) compared with whole blood (WB). CN activity was measured in peripheral blood leukocytes (PBL) that ha d been exposed in vitro to CsA in either WE or CRI. Cells from both gr oups were also stimulated with OKT3 to determine the effect of CsA on the induction of IFN-gamma synthesis. CsA accumulation in PBL was dete rmined by liquid scintillation counting of PBL exposed to H-3-CsA. The IC50 for CsA inhibition of CN activity was significantly lower for PB L in CRI (2 mu g/L) compared with PBL in WE (102 mu g/L, P less than o r equal to 0.005). Likewise, for CsA inhibition of IFN-gamma induction , the IC50 was 18 mu g/L for PBL in CM compared with 690 mu g/L for PB L in WE (P less than or equal to 0.005). The shift in IC50 was accompa nied by a 10-fold increase in H-3-CsA in PBL in CM compared with PBL i n WB. We conclude that PBL exposed to CsA in CM accumulate significant ly more CsA than PBL in WE. The result is that CsA inhibition of CN ac tivity and cytokine induction appears at least an order of magnitude g reater than its true effect in biologic fluids. This disparity is due to partitioning of CsA to irrelevant CsA binding sites, which are abun dant in WE and in vivo, but absent in culture medium.