Hemopoiesis-stimulating effects and enhanced survival of irradiated mice after peroral or intraperitoneal administration of ultrafiltered pig leukocyte extract (UPLE, IMUNOR)
Language English Country England, Great Britain Media print
Document type Journal Article
PubMed
12510796
DOI
10.1081/iph-120016049
Knihovny.cz E-resources
- MeSH
- Administration, Oral MeSH
- Cell Extracts MeSH
- Colony-Stimulating Factors pharmacology MeSH
- Hematopoietic Stem Cells drug effects MeSH
- Hematopoiesis drug effects radiation effects MeSH
- Injections, Intraperitoneal MeSH
- Interleukin-3 pharmacology MeSH
- Leukocytes physiology MeSH
- Mice MeSH
- Swine MeSH
- Radiation-Protective Agents pharmacology MeSH
- Tissue Extracts physiology MeSH
- Ultrafiltration MeSH
- Animals MeSH
- Check Tag
- Mice MeSH
- Female MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- Cell Extracts MeSH
- Colony-Stimulating Factors MeSH
- IMUNOR MeSH Browser
- Interleukin-3 MeSH
- Radiation-Protective Agents MeSH
- Tissue Extracts MeSH
Ultrafiltered pig leukocyte extract (UPLE, IMUNOR, ImunomedicA, Ustí nad Labem, Czech Republic) administered perorally (p.o.) or intraperitoneally (i.p.) enhanced recovery of the pool of granulocyte-macrophage hemopoietic progenitor cells (GM-CFC) in the bone marrow of normal or sublethally irradiated mice and increased survival of mice exposed to a lethal radiation dose. In experiments in vitro, sera of mice treated with UPLE p.o. or i.p. induced GM-CFC colony formation in cultures of normal mouse bone marrow cells, i.e., produced colony-stimulating activity (CSA). UPLE alone did not induce GM-CFC colony growth, i.e., had no CSA. When UPLE alone or sera of mice administered UPLE p.o. or i.p. were added to bone marrow cultures containing suboptimal concentration of recombinant mouse interleukin-3 (rmIL-3), both UPLE and the sera increased the counts of GM-CFC colonies in comparison with cultures containing only rmIL-3, i.e., produced co-stimulating activity (CoSA). Based on the findings obtained in vitro, it can be hypothesized that the described CSA and CoSA of UPLE may play a role also under in vivo conditions; enhancement of the recovery of hemopoiesis suppressed by ionizing radiation may be due to co-operation of the stimulatory effects of UPLE with the action of cytokines endogenously produced in irradiated tissues.
References provided by Crossref.org
Physicochemical Characterization of the Oral Biotherapeutic Drug IMUNOR®