Splenic irradiation combined with tumor irradiation promotes T cell infiltration in the tumor microenvironment and helps in tumor control

被引:8
|
作者
Chen, Hai-yan [1 ,2 ]
Xie, Hua-ying [1 ]
Liu, Xiao-xing [1 ]
Li, Lin-feng [2 ]
Bai, Yong-rui [1 ]
Gao, Jian-xin [2 ]
机构
[1] Shanghai Jiao Tong Univ, Sch Med, Ren Ji Hosp, Dept Radiat Oncol, 160 Pujian Rd, Shanghai 200127, Peoples R China
[2] Shanghai Jiao Tong Univ, Sch Med, Ren Ji Hosp, State Key Lab Oncogenes & Related Genes,Renji Med, 160 Pujian Rd, Shanghai 200127, Peoples R China
基金
中国国家自然科学基金;
关键词
Splenic irradiation; Tumor infiltrating leucocytes; Tumor microenvironment; IL-1; beta; CXCR3; B-LYMPHOCYTES; RADIATION; RADIOTHERAPY; CANCER; EXPRESSION; IMMUNITY; INNATE;
D O I
10.1016/j.bbrc.2019.01.071
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Locally applied radiation to the tumor is reported to stimulate systemic immune response. During radiotherapy to the abdominal cancer, spleen often receives certain dose, though as an important immune organ, little is known about the impact of splenic irradiation (SI) on systemic immune and local tumor control. Through a mice model, we found that the combination of SI with tumor irradiation (TI) helped in local control. The analysis of the tumor infiltrating leucocytes demonstrated that SI plus TI brought more T cell aggregation in the tumor microenvironment (TME), which helped in tumor control. Increased T cell infiltration may be partly due to higher expression of T cell chemokine in the TME and more expression of CXCR3 on the T cells in the spleen after SI. SI produced more IL-1 beta in the spleen, IL-1 beta stimulated the expression of CXCR3 on the T cells, and enhanced their migration ability. Taken together, radiation to the spleen combined with TI helped in local control through promoting T cell infiltration, and may be a considerable means to enhance the immunomodulatory of radiotherapy. (C) 2019 Published by Elsevier Inc.
引用
收藏
页码:156 / 162
页数:7
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