高级检索
当前位置: 首页 > 详情页

Immune response of γδT cells in Schistosome japonicum-infected C57BL/6 mouse liver

文献详情

资源类型:
WOS体系:

收录情况: ◇ SCIE

机构: [1]Functional Experiment Centre, Guangzhou Medical University, Guangzhou, China, [2]Department of Laboratory Medicine, Third Affiliated Hospital, Guangzhou Medical University, Guangzhou, China, [3]Department of Pathogenic Biology and Immunology, institute of immunology, Guangzhou Medical University, Guangzhou, China, [4]Institute of Immunology, Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou, China, [5]Key Laboratory of Tropical Disease Control Research of Ministry of Education, Sun Yat-sen University, Guangzhou, China, [6]Department of Pharmacology, Vanderbilt University, Nashville, TN, USA, [7]Department of Infectious Diseases, Affiliated No.8 Guangzhou Peoples Hospital, Guangzhou Medical University, Guangzhou, China, [8]Clinical laboratory, Traditional Chinese Medicine Hospital of Guangdong province, Guangzhou, China
出处:
ISSN:

关键词: cytokines NKG2D Schistosoma japonicum T cell

摘要:
Systematic evaluation of the role of T cells during the Schistosoma japonicum infection has not been reported, despite the fact that T cells contribute to many infectious diseases in innate immunity. Therefore, the aim of this study was to observe the properties of T cells in the liver of C57BL/6 mice infected by S.japonicum. In this report, using immuno-fluorescent histological analysis, T cells were found around hepatic granulomatous. Moreover, the flow cytometry results revealed that the percentage of hepatic T cells increased significantly after S.japonicum infection. More interestingly, a subset of CD3(-)TCR(+) cells were found and markedly increased after infection. Furthermore, expression of activation markers (CD25 and CD69) and cytokine profiles were detected in these hepatic CD3(+)TCR(+)and CD3(-)TCR(+) cells. The significantly higher level of CD69, IL-4 and IL-17 were observed in CD3(+)TCR(+) cells after infection, suggesting that CD3(+)TCR(+) cells instead of CD3(-)TCR(+) cells might play a predominant role during the infection. Finally, our results indicated that the expression of NKG2D on CD3(+)TCR(+) cells was higher than that on CD3(-)TCR(+) cells. Collectively, T cells could play an important role in the liver of C57BL/6 mouse during japonicum infection.

基金:

基金编号: 30901353 2011J22007 2012C117

语种:
被引次数:
WOS:
PubmedID:
中科院(CAS)分区:
出版当年[2013]版:
大类 | 3 区 医学
小类 | 3 区 寄生虫学 4 区 免疫学
最新[2025]版:
大类 | 4 区 医学
小类 | 4 区 免疫学 4 区 寄生虫学
JCR分区:
出版当年[2012]版:
Q2 PARASITOLOGY Q3 IMMUNOLOGY
最新[2023]版:
Q3 PARASITOLOGY Q4 IMMUNOLOGY

影响因子: 最新[2023版] 最新五年平均 出版当年[2012版] 出版当年五年平均 出版前一年[2011版] 出版后一年[2013版]

第一作者:
第一作者机构: [1]Functional Experiment Centre, Guangzhou Medical University, Guangzhou, China,
共同第一作者:
通讯作者:
通讯机构: [3]Department of Pathogenic Biology and Immunology, institute of immunology, Guangzhou Medical University, Guangzhou, China, [8]Clinical laboratory, Traditional Chinese Medicine Hospital of Guangdong province, Guangzhou, China [*1]Department of Pathogenic Biology and Immunology, Guangzhou Medical College, 510182 Guangzhou, China [*2]Clinical laboratory, Traditional Chinese Medicine Hospital of Guangdong province, 510120 Guangzhou, China
推荐引用方式(GB/T 7714):
APA:
MLA:

资源点击量:2020 今日访问量:0 总访问量:646 更新日期:2024-07-01 建议使用谷歌、火狐浏览器 常见问题

版权所有©2020 广东省中医院 技术支持:重庆聚合科技有限公司 地址:广州市越秀区大德路111号