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Query: UMLS:C0036690 (
sepsis
)
59,461
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
Sepsis
-induced immunosuppression is recognized as one of the main features responsible for therapeutic failures. Myeloid-derived suppressor cells (MDSCs), which are mainly characterized by their suppressive properties, have been reported to be expanded in
sepsis
.
Ferumoxytol
(
FMT
), an FDA-approved iron supplement, has been shown to possess immune-modulatory properties in tumors. However, it is unclear whether
FMT
alters the functions of MDSCs to reduce late-
sepsis
immunosuppression. Here, we showed an immunomodulatory effect of
FMT
on MDSCs to ameliorate lipopolysaccharide (LPS)-induced immunosuppression in the late stage of
sepsis
. Separation of cells with internalized
FMT
and detection of the intracellular iron content showed that MDSCs could uptake
FMT
. Low doses of
FMT
had no effects on the cell viability of MDSCs, but
FMT
inhibited the expansion of MDSCs in vitro. Moreover,
FMT
significantly downregulated the expression levels of Arg-1, S100A8, S100A9, and p47phox as well as ROS production in MDSCs.
FMT
decreased the percentage of granulocytic MDSCs (G-MDSCs) and promoted the differentiation of MDSCs into macrophages. Furthermore,
FMT
reduced white blood cell recruitment and alveolar wall thickening in the lungs and areas of necrosis in the liver as well as some biochemical markers of liver dysfunction.
FMT
decreased the percentage of G-MDSCs and monocytic MDSCs (M-MDSCs) in the spleens of LPS-induced septic mice. Of note,
FMT
reduced the T cell immunosuppressive functions of both G-MDSCs and M-MDSCs. Expectedly,
FMT
also significantly reduced Arg-1 and p47phox gene expression in splenic CD11b
+
Gr-1
+
cells isolated from LPS-challenged mice. These data indicate that
FMT
decreased the immunosuppressive functions of MDSCs by decreasing Arg-1 and ROS production, suggesting that
FMT
may reduce long-term immunosuppression in the late stage of
sepsis
.
...
PMID:Ferumoxytol Attenuates the Function of MDSCs to Ameliorate LPS-Induced Immunosuppression in Sepsis. 3184 96