Activation and Cytotoxicity of Bone Marrow Immunocytes by Using Various Cytokines
- Author:
Wen-Rong HUANG
1
;
Chun-Ji GAO
;
Bo-Long ZHANG
;
Hai-Jie JIN
;
Wan-Ming DA
Author Information
1. Depatment of Hematology, The General Hospital of PLA, Beijing 100853, China.
- Publication Type:Journal Article
- From:
Journal of Experimental Hematology
2001;9(1):48-51
- CountryChina
- Language:Chinese
-
Abstract:
The study aimed to explore the changes of the immunocyte quantities and cytotoxicity in bone marrow, and how many hematopoietic progenitor cells retained after the bone marrow cells were activated by different combinations of various cytokines. Bone marrow cells were divided into four groups and were cultured in vitro: (1) Control: no cytokines were added. (2) IL-2 group: bone marrow cells were activated by IL-2. (3) CD3-AK group: bone marrow cells were activated by IL-2 and CD3-McAb. (4) CIK group: IFN-gamma, IL-1, IL-2 and CD3-McAb were added. CFU-GM assay and CD3 phenotype detection were performed before and after activating culture in all groups. The changes of cell quantities during culture and cytotoxicity of cultured cells were tested. CD3 positive cells markedly increased in both CD3-AK and CIK groups. The cell numbers and cytotoxicity of CD3-AK and CIK groups were higher than those of control or IL-2 group obviously after culture (P < 0.05). CFU-GM were decreased in all groups after culture and there had no significant difference among four groups. The combination of IL-2 and CD3-McAb not only stimulates the proliferation of marrow immunocytes and increases their cytotoxicity but retains enough hematopoietic progenitor cells as well. This combination of cytokines can be used to purge autologous bone marrow in vitro.
