共 136 条
Myeloid-Derived Suppressor Cells in Bacterial Infections
被引:100
作者:

Ost, Michael
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机构:
Univ Tubingen, Childrens Hosp, Tubingen, Germany Univ Tubingen, Childrens Hosp, Tubingen, Germany

Singh, Anurag
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h-index: 0
机构:
Univ Tubingen, Childrens Hosp, Tubingen, Germany Univ Tubingen, Childrens Hosp, Tubingen, Germany

Peschel, Andreas
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Tubingen, Dept Infect Biol, Interfac Inst Microbiol & Infect Med, Tubingen, Germany Univ Tubingen, Childrens Hosp, Tubingen, Germany

Mehling, Roman
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Tubingen, Childrens Hosp, Tubingen, Germany Univ Tubingen, Childrens Hosp, Tubingen, Germany

Rieber, Nikolaus
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h-index: 0
机构:
Univ Tubingen, Childrens Hosp, Tubingen, Germany
Tech Univ Munich, Dept Pediat, Kinderklin Munchen Schwabing, Klinikum Schwabing,StKM GmbH, D-80290 Munich, Germany
Tech Univ Munich, Klinikum Rechts Isar, D-80290 Munich, Germany Univ Tubingen, Childrens Hosp, Tubingen, Germany

Hartl, Dominik
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h-index: 0
机构:
Univ Tubingen, Childrens Hosp, Tubingen, Germany Univ Tubingen, Childrens Hosp, Tubingen, Germany
机构:
[1] Univ Tubingen, Childrens Hosp, Tubingen, Germany
[2] Univ Tubingen, Dept Infect Biol, Interfac Inst Microbiol & Infect Med, Tubingen, Germany
[3] Tech Univ Munich, Dept Pediat, Kinderklin Munchen Schwabing, Klinikum Schwabing,StKM GmbH, D-80290 Munich, Germany
[4] Tech Univ Munich, Klinikum Rechts Isar, D-80290 Munich, Germany
来源:
FRONTIERS IN CELLULAR AND INFECTION MICROBIOLOGY
|
2016年
/
6卷
关键词:
MDSC;
myeloid-derived suppressor cells;
bacteria;
infection;
immune suppression;
sepsis;
PSEUDOMONAS-AERUGINOSA INFECTION;
NITRIC-OXIDE;
IMMUNE-RESPONSE;
T-CELLS;
TUBERCULOSIS INFECTION;
CLINICAL-SIGNIFICANCE;
PATTERN-RECOGNITION;
CARCINOMA PATIENTS;
CYSTIC-FIBROSIS;
DENDRITIC CELLS;
D O I:
10.3389/fcimb.2016.00037
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
Myeloid-derived suppressor cells (MDSCs) comprise monocytic and granulocytic innate immune cells with the capability of suppressing T- and NK-cell responses. While the role of MDSCs has been studied in depth in malignant diseases, the understanding of their regulation and function in infectious disease conditions has just begun to evolve. Here we summarize and discuss the current view how MDSCs participate in bacterial infections and how this knowledge could be exploited for potential future therapeutics.
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