FOLLOWUS
National Hematological Medical Center of Traditional Chinese Medicine, Department of Hematology, Xiyuan Hospital, China Academy of Chinese Medical Sciences,Beijing,China
纸质出版日期:2010,
网络出版日期:2010-9-25,
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Xu, Yg., Ma, R., Yang, Xh. et al. Effect of Yiqi Bushen Granule (益气补肾颗粒) on the peripheral natural killer cell and γ δ T-cell in the patients with minimal residual leukemia., Chin. J. Integr. Med. 16, 417–421 (2010). https://doi.org/10.1007/s11655-010-0536-7
Yong-gang Xu, Rou Ma, Xiao-hong Yang, et al. Effect of Yiqi Bushen Granule (益气补肾颗粒) on the peripheral natural killer cell and γ δ T-cell in the patients with minimal residual leukemia[J]. Chinese Journal of Integrative Medicine, 2010,16(5):417-421.
Xu, Yg., Ma, R., Yang, Xh. et al. Effect of Yiqi Bushen Granule (益气补肾颗粒) on the peripheral natural killer cell and γ δ T-cell in the patients with minimal residual leukemia., Chin. J. Integr. Med. 16, 417–421 (2010). https://doi.org/10.1007/s11655-010-0536-7 DOI:
Yong-gang Xu, Rou Ma, Xiao-hong Yang, et al. Effect of Yiqi Bushen Granule (益气补肾颗粒) on the peripheral natural killer cell and γ δ T-cell in the patients with minimal residual leukemia[J]. Chinese Journal of Integrative Medicine, 2010,16(5):417-421. DOI: 10.1007/s11655-010-0536-7.
To analyze the changes in peripheral natural killer T-cells (NKT) and gammadelta T-cells (γ δ T-cell) in patients with minimal residual leukemia (MRL) before and after being treated with Yiqi Bushen Granule (益气补肾颗粒
YBG) in order to determine their significance in prognosis of the disease. Granule (益气补肾颗粒
YBG) in order to determine their significance in prognosis of the disease. Before and after treatment
the changes in 36 patients (16 males and 20 females) receiving long-term (more than 3 months) YBG therapy were analyzed using multi-parameter flow cytometry
with 34 healthy persons (19 males and 15 females) acting as controls. males and 15 females) acting as controls. The absolute value and percentage of NKT cells and γ δ T-cells were all significantly raised after treatment
for NKT cells
0.52%±0.39% to 0.83%±0.66% and 7.25±7.77 cells cell/μL to 12.86±11.99 cell/μL
for γ δ T-cells
6.08%±3.03% to 7.24%±2.78% and 83.97±48.09 cell/μL 110.53±54.12 cell/μL
respectively (P<0.05 or P<0.01). YBG could regulate the immune function and elevate the amount of NKT cells and γ δ T-cells
thus to kill or suppress the residual leukemic cell in the body
which might be one of the mechanisms of YBG in prolonging the disease-free survival in MRL patients.
To analyze the changes in peripheral natural killer T-cells (NKT) and gammadelta T-cells (γ δ T-cell) in patients with minimal residual leukemia (MRL) before and after being treated with Yiqi Bushen Granule (益气补肾颗粒
YBG) in order to determine their significance in prognosis of the disease. Granule (益气补肾颗粒
YBG) in order to determine their significance in prognosis of the disease. Before and after treatment
the changes in 36 patients (16 males and 20 females) receiving long-term (more than 3 months) YBG therapy were analyzed using multi-parameter flow cytometry
with 34 healthy persons (19 males and 15 females) acting as controls. males and 15 females) acting as controls. The absolute value and percentage of NKT cells and γ δ T-cells were all significantly raised after treatment
for NKT cells
0.52%±0.39% to 0.83%±0.66% and 7.25±7.77 cells cell/μL to 12.86±11.99 cell/μL
for γ δ T-cells
6.08%±3.03% to 7.24%±2.78% and 83.97±48.09 cell/μL 110.53±54.12 cell/μL
respectively (P<0.05 or P<0.01). YBG could regulate the immune function and elevate the amount of NKT cells and γ δ T-cells
thus to kill or suppress the residual leukemic cell in the body
which might be one of the mechanisms of YBG in prolonging the disease-free survival in MRL patients.
minimal residual leukemiaYiqi Bushen Granulenatural killer T-cellgamma-delta T-cell
minimal residual leukemiaYiqi Bushen Granulenatural killer T-cellgamma-delta T-cell
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Xu YG, Ma R, Hu NP, Liu F, Yang JM, Ma L, et al. Effect of Fuzheng Kangbai Granule (扶正抗白冲剂) on immune function and survival time in minimal residual leukemia model mice. Chin J Integr Med 2001;7:283–287.
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