Alpha-GalCer Administration after Allogeneic Bone Marrow Transplantation Improves Immune Reconstitution in Mice
Alpha-GalCer Administration after Allogeneic Bone Marrow Transplantation Improves Immune Reconstitution in Mice作者机构:Department of Hematology Shenyang Military General Hospital Shenyang 110016 China Department of Hematology General Hospital of the Chinese People's Liberation Army Beijing 100853 China
出 版 物:《Chinese Medical Sciences Journal》 (中国医学科学杂志(英文版))
年 卷 期:2011年第26卷第2期
页 面:91-97页
核心收录:
学科分类:0710[理学-生物学] 07[理学] 081302[工学-建筑设计及其理论] 08[工学] 0813[工学-建筑学] 071002[理学-动物学]
基 金:Supported by National Natural Science Foundation of China (30670898, 30572108) National Basic Research Program of China (973 Program) (2005CB522400) Capital Research Fund for Medical Development (2007-2040)
主 题:immune reconstitution α-galactosyleramide bone marrow transplantation
摘 要:Objective To explore the effect of α-galactosyleramide (α-GalCer) on immune reconstitution under acute graft-versus-host disease (aGVHD). Methods BALB/c mice were transplanted with allogeneic C57BL/6 bone marrow cells and splenocytes (both 1 × 10^7) after receiving lethal total-body irradiation, α-GalCer (100 ug/kg) or vehicle (dimethyl- sulfoxide) was administered intraperitoneally immediately after transplantation. The effects of α-GalCer on immune reconstitufion, proliferation of T cells and B cells, hematopoiesis, and thymic microenvironment were assessed. Results The α-GalCer group exhibited higher percentages of CD3^+, CD4^+, CD8^+, B220^+, CD40+, and CD86+cells compared with the vehicle group. The number of colony forming unit per 1000 CD34^+ cells in the et-GalCer group was higher than in the vehicle group (P=0.0012). In vitro proliferation assays showed that the α-GalCer group had higher percentages of CD3^+, CD4^+, CD8^+, and B220^+ cells compared with the vehicle group. As for the results of in vivo proliferation assays, the numbers of CD3^+, CD4^+, CD8^+, and B220^+ cells were higher in the α-GalCer group than in the normal group, especially the number of B220^+ cells (P=0.007). Significant difference was not found in thymocyte count between the α-GalCer group and the vehicle group, nor in the percentages of CD3^+, CD4^+, and CD8^+ cells. Conclusion Administration of tl-GalCer after allogeneic bone marrow transplantation may promote immune reconstitution in the presence of aGVHD.