Interleukin-19 Impairment in Active Crohn’s Disease Patients
Adult
Male
0301 basic medicine
Micro RNAs
Science
T cells
Lymphocyte Activation
Monocytes
03 medical and health sciences
Th2 Cells
Malaltia de Crohn
Resposta immunitària
Crohn Disease
Citoquines
Humans
CTLA-4 Antigen
Flow cytometry
Immune response
Leucocytes
Cells, Cultured
Aged
Leucòcits
Gene Expression Profiling
Interleukins
Q
Toll-Like Receptors
R
Middle Aged
Recombinant Proteins
Interleukin-10
3. Good health
Crohn's disease
MicroRNAs
Cèl·lules T
Gene Expression Regulation
Citometria de fluxe
Leukocytes, Mononuclear
Medicine
RNA
Cytokines
Female
Research Article
DOI:
10.1371/journal.pone.0093910
Publication Date:
2014-04-09T20:56:54Z
AUTHORS (12)
ABSTRACT
The exact function of interleukin-19 (IL-19) on immune response is poorly understood. In mice, IL-19 up-regulates TNFα and IL-6 expression its deficiency increases susceptibility to DSS-induced colitis. humans, favors a Th2 elevated in several diseases. We here investigate the effects cells from active Crohn’s disease (CD) patient. Twenty-three CD patients 20 healthy controls (HC) were included. mRNA protein levels analyzed monocytes. determined vitro T cell phenotype production cytokines by cells. observed that unstimulated TLR-activated monocytes expressed significantly lower than HC (logFC = −1.97 unstimulated; −1.88 with Pam3CSK4; −1.91 FSL-1; p<0.001). These results confirmed at level. Exogenous had an anti-inflammatory effect but not patients. decreased PBMC (850.7±75.29 pg/ml vs 2626.0±350 pg/ml; p<0.01) increased CTLA4 (22.04±1.55% 13.98±2.05%; p<0.05) IL-4 (32.5±8.9 13.5±2.9 HC. IL-10 regulated both three miRNAs can modulate expression, up-regulated suggested role this study. Defects lack cytokine could contribute inflammatory mechanisms
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CITATIONS (16)
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