Protective, restorative, and therapeutic properties of recombinant colony-stimulating factors
- National Cancer Institute-Frederick Cancer Research Facility, MD (USA)
Pretreatment of mice with recombinant murine (rM) colony-stimulating factor-granulocyte-macrophage (CSF-gm) or recombinant human (rH) CSF-g provides partial protection from the lethal effects of ionizing radiation or the alkylating agent cyclophosphamide (CTX). In addition, these agents can significantly prolong survival if administered following lethal doses of irradiation or CTX. To induce protective activity, cytokines were injected 20 hours before lethal irradiation or CTX administration. To accelerate recovery from lethal irradiation, the cytokines must be administered shortly following irradiation, and the induction of maximal levels of activity is dependent on chronic administration. In contrast, because of their longer half-lives, accelerated recovery from alkylating agents requires a delay of at least 24 to 48 hours to allow complete clearance of CTX before administration of a CSF. Studies quantitating peripheral blood leukocytes and bone marrow cellularity as well as colony-forming units per culture (CFU-C) frequency and CFU-C per femur revealed a significant correlation between these parameters and the ability to survive lethal irradiation.
- OSTI ID:
- 5513231
- Journal Information:
- Blood; (USA), Vol. 73:8; ISSN 0006-4971
- Country of Publication:
- United States
- Language:
- English
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Related Subjects
MITOGENS
RADIOSENSITIVITY EFFECTS
BLOOD FORMATION
BONE MARROW
COLONY FORMATION
ENDOXAN
GROWTH FACTORS
INTRAPERITONEAL INJECTION
LETHAL IRRADIATION
LEUKOPENIA
MICE
ALKYLATING AGENTS
ANIMAL TISSUES
ANIMALS
BODY
DISEASES
DRUGS
HEMATOPOIETIC SYSTEM
HEMIC DISEASES
IMMUNE SYSTEM DISEASES
IMMUNOSUPPRESSIVE DRUGS
INJECTION
INTAKE
IRRADIATION
MAMMALS
ORGANIC COMPOUNDS
ORGANS
PROTEINS
RODENTS
TISSUES
VERTEBRATES
560152* - Radiation Effects on Animals- Animals