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2015 ; 157
(2
): 175-86
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Myeloid-derived suppressor cells are proinflammatory and regulate
collagen-induced arthritis through manipulating Th17 cell differentiation
#MMPMID25680967
Zhang H
; Wang S
; Huang Y
; Wang H
; Zhao J
; Gaskin F
; Yang N
; Fu SM
Clin Immunol
2015[Apr]; 157
(2
): 175-86
PMID25680967
show ga
Myeloid-derived suppressor cells (MDSC) and Th17 cells were found to expand in
collagen-induced arthritis (CIA) significantly. Two subsets of MDSC,
polymorphonuclear (PMN) and mononuclear (MO), were detected and their ratios
varied during the development of CIA. The depletion of MDSC in vivo resulted in
suppression of T-cell proliferation and decreased IL-17A and IL-1? production.
The adoptive transfer of MDSC restored the severity of arthritis and Th17 cell
differentiation. The depletion of MDSCs on day 35 resulted in arthritis
amelioration without reaching a significant difference. Furthermore, MDSCs from
CIA mice had higher production of IL-1? and promoted Th17 cell differentiation.
The expansion of MDSCs in the peripheral blood of rheumatoid arthritis (RA)
patients was in correlation with increased Th17 cells and disease activity DAS28.
These results support the hypothesis that MDSC may play a significant
proinflammatory role in the pathogenesis of CIA and RA by inducing Th17
development in an IL-1?-dependent manner.