Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Clinical Trial
. 2003 Sep;94(9):814-20.
doi: 10.1111/j.1349-7006.2003.tb01524.x.

Mirimostim (macrophage colony-stimulating factor; M-CSF) improves chemotherapy-induced impaired natural killer cell activity, Th1/Th2 balance, and granulocyte function

Affiliations
Clinical Trial

Mirimostim (macrophage colony-stimulating factor; M-CSF) improves chemotherapy-induced impaired natural killer cell activity, Th1/Th2 balance, and granulocyte function

Takao Hidaka et al. Cancer Sci. 2003 Sep.

Abstract

The purpose of this study was to clarify the effects of mirimostim (macrophage colony-stimulating factor; M-CSF) on immunological functions after chemotherapy. The percentage of natural killer (NK) cells in peripheral blood mononuclear cells (PBMCs), NK cell activity, T-helper cell 1/T-helper cell 2 (Th1/Th2) ratio, and superoxide anion production by granulocytes (granulocyte function) were measured as immunological parameters before and after chemotherapy in 44 patients with primary ovarian cancer who received at least three consecutive courses of postoperative chemotherapy. Patients were observed during the first course of chemotherapy, and 39 patients who presented grade III or IV neutropenia were entered into this study and randomly allocated to an M-CSF-administered group (group 1; 19 patients) and a non-M-CSF-administered group (group 2; 20 patients) for the second course. For the third course, a crossover trial was conducted. In the observation period, chemotherapy significantly impaired the immunological parameters. In particular, those parameters were significantly decreased at day 14 compared to the level before chemotherapy. The values of the parameters of group 1 were significantly higher than those of group 2. In the course of chemotherapy during which M-CSF was administered, 19 of the 39 patients presented grade IV neutropenia, and received granulocyte colony-stimulating factor (G-CSF) between days 7 and 14. We compared the changes of those immunological parameters in the M-CSF alone group and the M-CSF + G-CSF group, and found that the concomitant use of G-CSF did not further improve the parameters. These results indicate that chemotherapy markedly impaired the immunological functions, and that the administration of M-CSF significantly improved the impaired immunological functions.

PubMed Disclaimer

References

    1. Hibi S, Yoshihara T, Nakajima F, Misu H, Mabuchi O, Imashuku S. Effect of recombinant human granulocyte‐colony stimulating factor (rhG‐CSF) on immune system in pediatric patients with a plastic anemia. Pediatr Hematol Oncol 1994; 11: 319–23. - PubMed
    1. Miller JS, Prosper F, McCullar V. Natural killer (NK) cells are functionally abnormal and NK cell progenitors are diminished in granulocyte colony‐stimulating factor‐mobilized peripheral blood progenitor cell collections. Blood 1997; 15: 3098–105. - PubMed
    1. Rondelli D, Raspadori D, Anasetti C, Bandini G, Re F, Arpinati M, Stanzani M, Morelli A, Baccini C, Zaccaria A, Lemoli RM, Tura S. Alloantigen presenting capacity, T cell alloreactivity and NK function of G‐CSF‐mobilized peripheral blood cells. Bone Marrow Transplant 1998; 22: 631–7. - PubMed
    1. Klangsinsirikul P, Russell NH. Peripheral blood stem cell harvests from G‐CSF‐stimulated donors contain a skewed Th2 CD4 phenotype and a predominance of type 2 dendritic cells. Exp Hematol 2002; 30: 495–501. - PubMed
    1. Valente JF, Alexander JW, Li BG, Noel JG, Custer DA, Ogle JD, Ogle CK. Effect of in vivo infusion of granulocyte colony‐stimulating factor on immune function. Shock 2002; 17: 23–9. - PubMed

MeSH terms

Substances