Clinical significance and functional studies of myeloid-derived suppressor cells in chronic hepatitis C patients. (Q42277377)

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22 February 2020

title

Clinical significance and functional studies of myeloid-derived suppressor cells in chronic hepatitis C patients (English)

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22 February 2020

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4

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22 February 2020

author name string

Weiping Cai

1

1 reference

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22 February 2020

Aiping Qin

2

1 reference

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22 February 2020

Pengle Guo

3

1 reference

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22 February 2020

Fengyu Hu

5

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22 February 2020

Qiong Yang

6

1 reference

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22 February 2020

Min Xu

7

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22 February 2020

Yongshui Fu

8

1 reference

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22 February 2020

Jie Zhou

9

1 reference

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22 February 2020

Xiaoping Tang

10

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22 February 2020

publication date

26 January 2013

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Journal of Clinical Immunology

22 February 2020

published in

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22 February 2020

volume

33

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22 February 2020

issue

4

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22 February 2020

page(s)

798-808

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https://scigraph.springernature.com/pub.10.1007/s10875-012-9861-2

22 February 2020

exact match

0 references

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Invariant NKT cells reduce the immunosuppressive activity of influenza A virus-induced myeloid-derived suppressor cells in mice and humans

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Myeloid suppressor cells induced by hepatitis C virus suppress T-cell responses through the production of reactive oxygen species

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Serum HCV RNA levels correlate with histological liver damage and concur with steatosis in progression of chronic hepatitis C.

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PD-1 expression on peripheral CD8+ TEM/TEMRA subsets closely correlated with HCV viral load in chronic hepatitis C patients

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Histological changes in HCV antibody-positive, HCV RNA-negative subjects suggest persistent virus infection

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Cytokine--chemokine and apoptotic signatures in patients with hepatitis C.

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Kinetics of serum cytokines reflect changes in the severity of chronic hepatitis C presenting minimal fibrosis

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Systemic and intrahepatic interferon-gamma-inducible protein 10 kDa predicts the first-phase decline in hepatitis C virus RNA and overall viral response to therapy in chronic hepatitis C

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Human CD4(+)CD25(+) cells: a naturally occurring population of regulatory T cells.

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