Additive Effects of Human Recombinant Interleukin-11 and Granulocyte Colony-Stimulating Factor in Experimental Gram-Negative Sepsis
Open Access
- 15 May 1999
- journal article
- Published by American Society of Hematology in Blood
- Vol. 93 (10) , 3467-3472
- https://doi.org/10.1182/blood.v93.10.3467.410k10_3467_3472
Abstract
Recombinant human granulocyte colony-stimulating factor (rhG-CSF) is widely used to promote granulocyte recovery from a variety of pathologic states. Recombinant human interleukin-11 (rhIL-11) has recently become available clinically as a platelet restorative agent after myelosuppressive chemotherapy. Preclinical data has shown that rhIL-11 limits mucosal injury after chemotherapy and attenuates the proinflammatory cytokine response. The potential efficacy of combination therapy with recombinant human forms of rhIL-11 and rhG-CSF was studied in a neutropenic rat model of Pseudomonas aeruginosa sepsis. At the onset of neutropenia, animals were randomly assigned to receive either rhG-CSF at a dose of 200 μg/kg subcutaneously every 24 hours for 7 days; rhIL-11 at 200 μg/kg subcutaneously every 24 hours for 7 days; the combination of both rhG-CSF and rhIL-11; or saline control. Animals were orally colonized with Pseudomonas aeruginosa 12.4.4 and then given a myelosuppressive dose of cyclophosphamide. rhG-CSF resulted in a slight increase in absolute neutrophil counts (ANC), but did not provide a survival advantage (0 of 12, 0% survival) compared with the placebo group (1 of 12 , 8% survival). rhIL-11 was partially protective (4 of 10, 40% survival); the combination of rhG-CSF and rhIL-11 resulted in a survival rate of 80% (16 of 20; P < .001). rhIL-11 alone or in combination with rhG-CSF resulted in preservation of gastrointestinal mucosal integrity (P < .001), lower circulating endotoxin levels (P < .01), and reduced quantitative levels of P. aeruginosa in quantitative organ cultures. These results indicate that the combination of rhIL-11 and rhG-CSF is additive as a treatment strategy in the prevention and treatment of experimental Gram-negative sepsis in immunocompromised animals. This combination may prove to be efficacious in the prevention of severe sepsis in neutropenic patients.Keywords
This publication has 32 references indexed in Scilit:
- Interleukin-11 promotes T cell polarization and prevents acute graft-versus-host disease after allogeneic bone marrow transplantation.Journal of Clinical Investigation, 1998
- Interleukin-11BioDrugs, 1997
- Anti-inflammatory therapies to treat sepsis and septic shockCritical Care Medicine, 1997
- Granulocyte colony-stimulating factor improves survival rate and reduces concentrations of bacteria, endotoxin, tumor necrosis factor, and endothelin-1 in fulminant intra-abdominal sepsis in ratsCritical Care Medicine, 1996
- Molecular Cloning and Characterization of the Human Interleukin-11 Receptor α-Chain Gene, IL11RA, Located on Chromosome 9p13Genomics, 1996
- The biology of interleukin 11The International Journal of Cell Cloning, 1996
- Clinical development of recombinant human interleukin-11 to treat chemotherapy-induced thrombocytopeniaCurrent Opinion in Hematology, 1996
- Interleukin‐11 protects the clonogenic stem cells in murine small‐intestinal crypts from impairment of their reproductive capacity by radiationInternational Journal of Cancer, 1995
- Recombinant human granulocyte colony-stimulating factor enhances superoxide release in human granulocytes stimulated by the chemotactic peptideBiochemical and Biophysical Research Communications, 1987
- Human granulocyte-macrophage colony-stimulating factor is a neutrophil activatorNature, 1985