Stem Cell Transfusion Restores Immune Function in Radiation-Induced Lymphopenic C57BL/6 Mice

被引:15
作者
Kapoor, Vaishali [1 ]
Khudanyan, Arpine [1 ]
de la Puente, Pilar [1 ]
Campian, Jian [2 ,3 ]
Hallahan, Dennis E. [1 ,2 ,4 ]
Azab, Abdel Kareem [1 ,2 ]
Thotala, Dinesh [1 ,2 ]
机构
[1] Washington Univ, Sch Med, Dept Radiat Oncol, St Louis, MO 63108 USA
[2] Washington Univ, Sch Med, Siteman Canc Ctr, St Louis, MO 63108 USA
[3] Washington Univ, Sch Med, Div Oncol, Dept Med, St Louis, MO 63108 USA
[4] Washington Univ, Sch Med, Mallinckrodt Inst Radiol, St Louis, MO 63108 USA
关键词
ADENOCARCINOMA; ASSOCIATION;
D O I
10.1158/0008-5472.CAN-15-1412
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Radiation-induced lymphopenia (RIL) is associated with treatment of different tumors (lung, colon, pancreas, breast, sarcomas, and glioblastoma). It is a significant clinical problem affecting the survival of cancer patients. The biologic mechanisms leading to RIL are not clearly understood. In this study, we established a mouse model of RIL representing therapeutic clinical regimen for lung cancer. Flow cytometry was used to analyze circulating levels of T and B cells and bone marrow (BM) stem cells. We found that fractionated radiation to the thorax significantly reduced circulating T and B cells as well as BM stem cells. Ex-vivo irradiation of blood and autologous reinjection to mice also significantly induced lymphopenia. Furthermore, we found that mobilization of stem cells from the BM and autologous stem cell transplant rescued RIL in mice. Overall, our results suggest that RIL has not only direct effect on circulating lymphocytes, but also has indirect effect on circulating lymphocytes as well as stem cells in the nonirradiated BM. These results open a new window for investigating the direct and indirect biologic mechanisms leading to RIL, and provide a preclinical basis to test the effect of stem cell transplantation for treatment of RIL in cancer patients. (C)2015 AACR.
引用
收藏
页码:3442 / 3445
页数:4
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