<p>Scatter dot plots show relative mRNA expression levels in PBMCs from MS patients before (t0) or after 3 months (t3) of treatment by fingolimod, and healthy controls (HC) analysed by q-PCR. For each target, individual mRNA levels were expressed as relative values to the mean level of the control group. The mRNA expression levels of CD39 (p = 0.0033), as well as of AHR (p = 0.007) and CYP1B1, an AHR-induced gene (p<0.0001) were increased after fingolimod treatment. On the contrary, fingolimod reduced the mRNA levels of IL-17, IL-22 and FOXP3. Horizontal lines represent the median value in all subgroups. *, ** and *** indicate p-values of ≤0.05, ≤0.01 and ≤0.001 respectively.</p
BackgroundFingolimod is a sphingosine 1-phosphate receptor modulator approved for relapsing MS. Long...
a)IL-33 levels are correlated with expression of multiple genes during MS relapse and remission. mRN...
Objective: To establish cytometry profiles associated with disease stages and immunotherapy in MS. M...
<p>Effects of fingolimod on IFNγ- (A), IL17- (B), IL9- (C), and IL4-producing (D) cells in CD4<sup>+...
<p>Regulatory T cells of MS patients before (t0, n = 16) or after three months of treatment by fingo...
Multiple sclerosis (MS) likely results from an imbalance between regulatory and inflammatory immune ...
BACKGROUND: Multiple sclerosis (MS) likely results from an imbalance between regulatory and inflamma...
<p>The median and range are shown. Lymphoid cells were gated according to their FSC/SSC profile.</p>...
<p>(A.) Percentage of PB follicular helper T cells (T<sub>FH</sub>) in MS patients treated with fing...
<p>PBMCs of MS patients before (t0, n = 16) or after three months of treatment by fingolimod (t3, n ...
<p>Quantitative-PCR to measure IL-22 mRNA expression (A) <i>ex vivo</i> (Relapsing MS: n = 56, Stabl...
The long term effects of fingolimod, an oral treatment for relapsing-remitting (RR) multiple scleros...
Abstract Multiple sclerosis (MS) is a complex neurological disease where, in genetically predisposed...
<p>Expression levels of TLR1-10, MyD88, and MX1 mRNA were determined in PBMCs of 25 patients with RR...
<p>Effects of fingolimod on phenotypically distinct CD4<sup>+</sup>T (A) and CD8<sup>+</sup>T (B) ce...
BackgroundFingolimod is a sphingosine 1-phosphate receptor modulator approved for relapsing MS. Long...
a)IL-33 levels are correlated with expression of multiple genes during MS relapse and remission. mRN...
Objective: To establish cytometry profiles associated with disease stages and immunotherapy in MS. M...
<p>Effects of fingolimod on IFNγ- (A), IL17- (B), IL9- (C), and IL4-producing (D) cells in CD4<sup>+...
<p>Regulatory T cells of MS patients before (t0, n = 16) or after three months of treatment by fingo...
Multiple sclerosis (MS) likely results from an imbalance between regulatory and inflammatory immune ...
BACKGROUND: Multiple sclerosis (MS) likely results from an imbalance between regulatory and inflamma...
<p>The median and range are shown. Lymphoid cells were gated according to their FSC/SSC profile.</p>...
<p>(A.) Percentage of PB follicular helper T cells (T<sub>FH</sub>) in MS patients treated with fing...
<p>PBMCs of MS patients before (t0, n = 16) or after three months of treatment by fingolimod (t3, n ...
<p>Quantitative-PCR to measure IL-22 mRNA expression (A) <i>ex vivo</i> (Relapsing MS: n = 56, Stabl...
The long term effects of fingolimod, an oral treatment for relapsing-remitting (RR) multiple scleros...
Abstract Multiple sclerosis (MS) is a complex neurological disease where, in genetically predisposed...
<p>Expression levels of TLR1-10, MyD88, and MX1 mRNA were determined in PBMCs of 25 patients with RR...
<p>Effects of fingolimod on phenotypically distinct CD4<sup>+</sup>T (A) and CD8<sup>+</sup>T (B) ce...
BackgroundFingolimod is a sphingosine 1-phosphate receptor modulator approved for relapsing MS. Long...
a)IL-33 levels are correlated with expression of multiple genes during MS relapse and remission. mRN...
Objective: To establish cytometry profiles associated with disease stages and immunotherapy in MS. M...