Effects of erythropoietin-induced hemopoiesis on peritoneal transport and on in vitro T cell response in CAPD

Adv Perit Dial. 1992:8:453-6.

Abstract

In order to investigate the therapeutic efficacy of subcutaneously administered erythropoietin (rHuEPO) and the effects of rHuEPO-induced hemopoiesis on peritoneal transport and on cellular immune responses, we performed standardized peritoneal equilibration tests and measured T cell subsets and phytohemagglutinin (PHA)-induced interleukin-2 receptor (IL-2R) expression of PBMC by flow cytometry before and after subcutaneous rHuEPO (Eprex-, Cilag), 4000 U twice weekly, in 13 stable CAPD patients. Hct increased from 21.3 +/- 3.4% to 30.0 +/- 4.8% after 1 mo and to 32.7 +/- 4.9% after 2 mon of rHuEPO. Drained volume after 4 hrs of dwell with 4.25% dialysate increased from 2,675 +/- 204 ml to 2,807 +/- 174 ml (P < 0.05). D4/P4 creatinine increased from 0.68 +/- 0.07 to 0.71 +/- 0.06 (P < 0.05) and creatinine clearance from 7.57 +/- 0.71 to 8.03 +/- 0.63 ml/min (P < 0.05). The number of total circulating lymphocytes, T4,T8, T4/T8 with or without PHA did not change after rHuEPO. PHA-induced IL-2R expression by PBMC as expressed by mean channel of fluorescence intensity increased from 149.8 +/- 6.7 to 156.8 +/- 6.1 (P < 0.05).

Conclusion: Subcutaneous rHuEPO is effective in correcting anemia in CAPD patients. rHuEPO-induced hemopoiesis is associated with increase in peritoneal creatinine and water transport and also with PHA-induced IL-2R expression.

MeSH terms

  • Adult
  • Anemia / etiology
  • Anemia / therapy
  • Biological Transport
  • Erythropoietin / therapeutic use*
  • Female
  • Hematocrit
  • Hematopoiesis*
  • Hemoglobins / analysis
  • Humans
  • In Vitro Techniques
  • Leukocyte Count
  • Male
  • Monocytes / metabolism
  • Peritoneal Dialysis, Continuous Ambulatory*
  • Peritoneum / metabolism*
  • Phytohemagglutinins
  • Receptors, Interleukin-2 / metabolism
  • Recombinant Proteins / therapeutic use
  • T-Lymphocytes / immunology*

Substances

  • Hemoglobins
  • Phytohemagglutinins
  • Receptors, Interleukin-2
  • Recombinant Proteins
  • Erythropoietin