Захын Цусан Дахь Мононуклеар Цагаан Эсийн Хавдар Устгах Идэвхийг Шугаман Эсийн Загварт Тодорхойлсон Дүн
- VernacularTitle:Захын Цусан Дахь Мононуклеар Цагаан Эсийн Хавдар Устгах Идэвхийг Шугаман Эсийн Загварт Тодорхойлсон Дүн
- Author:
Nemekhbayar B
1
;
Gantulga D
1
;
Azzaya D
1
;
Batchimeg Ts
1
;
Erdenesaikhan T
1
;
Baigalmaa B
1
;
Bilegsaikhan D
1
;
Munkhbat B
1
Author Information
- Publication Type:Journal Article
- From: Journal of Oriental Medicine 2015;8(1):24-29
- CountryMongolia
- Language:Mongolian
- Abstract: Introduction: Cancer arises from abnormal cells nonstop divide in an uncontrolled way and without stopping. In GLOBOCAN reported that 14.1 million new cancer cases, 8.2 million cancer deaths and 32.6 million people suffering with cancer in 2012 worldwide. Among the world, a surgical, radiation and chemotherapy maintains the cancer treatment within their combination, and moreover, scientists believe that, in order to enhance the result and come up with better spotlight therapeutic outcome, immunotherapy should be added within combination of surgical, radiation and chemotherapy. Objective: To identify the immune ability of mononuclear cells in peripheral blood, and to study their cytolytic activity on cancer cellular line. Materials and method: Cytolytic activity assay was done with healthy human's PBMCs induced by non specific mytogen phytohemaglutinin L (PHA) of 10ul/ml, 5ul/ml, 2.5ul/ml dosage, and cultured with SP2Myeloma cell line. Then live cells and death cells analyzed with MTT assay and Propidium iodide, respectively, as well as CD+25 cells analyzed with Apogee flow cytometry at 24.48 and 72 hours of uncubation at 5% CO2, 37 C0. Result: Cancer Inhibition rate of mononuclear cells in blood (inhibition rate %) was assessed by МТТ assay and the culture of control group of mononuclear cells and myeloma cells’ median was (OD=0.36±0.05) while Phytohemaglutinin induced group’s result in 72 hours was (OD=0.31±0.03) which suggests that linear cells mononuclear cell’s mixture rate is 86.1%. Dead cell’s number assessed by Propidiumiodid (Cell toxicity assay) shows the result of control group’s cell death (10.68±2.1%), while Phytohemaglutinin induced group it was 20-25% which is statistically significant. (p<0.05). Cancer elimination activity assessed by СD25+ Т cells and the result of CD25+ Т number activated by Phytohemaglutinin (152-282 cell/µl), in control group (26cell/µl) which is statistically significant(p<0.001). Conclusion: 1. Myeloma SP2/0 cell line is inhibited the growth by peripheral mononuclear cells and it is not dependent dosage of Phytohemaglutinin. 2. Death of cell assessed by propidium iodide, control group’s cell death 10.68±2.1%, while Phytohemaglutinin induced group it was 20-25% which is statistically significant (p<0.05). 3. Cancer elimination activation assessed by СD25+ Т cells shows the result of CD25+ Т number activated by Phytohemaglutinin (152-282cell/µl), in control group (26cell/µl) which is statistically significant(p<0.001).
