(redirected from FOXP3)
Also found in: Dictionary, Medical, Wikipedia.
Related to FOXP3: CD25
Graphic Thesaurus  🔍
Display ON
Animation ON
  • noun

Synonyms for dieter


Words related to dieter

a person who diets

References in periodicals archive ?
has published a proof-of-concept study in OncoImmunology entitled "Depleting T regulatory cells by targeting intracellular Foxp3 with a TCR mimic antibody," the company said.
Each of the areas was photographed at 400x using the ImageJ[R] (Image Processing and Analysis in Java, National Institute of Mental Health, Bethesda, MD, USA) software, and the FoxP3 lymphocytes stained in each field were counted, regardless of the intensity of the brown staining.
Therefore, we explored the effect of TGF-[beta]1 on the expression of (20,21), IL-10, CTLA-4, and FoxP3 in CD4+CD25+ T cells.
For quantifying the transcription levels of ROR[gamma]t and Foxp3, total RNA (1 [micro]g) was extracted from the right lung tissue with TRIzol (Invitrogen, Life Technologies, USA) according to the manufacturer's instructions.
Observation of CD4+ RORg-T Th17 and CD25+ FOXP3 Treg were conducted with immunohistochemistry staining technique using anti FOX-P3 and anti RORg-T.
One study even revealed that the higher expression of EOMES in Th cell could result in the occurrence of secondary-progressive MS.[27] Another study conducted by Lupar et al .[28] revealed that the expression of EOMES limits the Foxp3 induction in a cell-intrinsic way.
In addition, RC byproducts activated the mRNA expression of galectin-9 in the MLN and spleen with increased T-bet and Foxp3 as a reflection of Th1 and Treg cells, respectively.
Some studies have shown that approximately 5% of Th cells in the blood express FOXP3, and about 20% of Th cells in the skin of adults.
Some researchers found although CD4+LAP+ T cells lack Foxp3 expression but they can secrete IL-10 and TGF-[beta] upon activation and exhibit immune-suppressive activity in vitro [9].
Considering the inconsistency of the available data on the number of Treg, their potentially important role in MDS pathogenesis, and functional differences between expressed FOXP3 isoforms, we decided to evaluate not only the number and percentage of Treg in this disease but also the level of FOXP3 isoforms expression in patients with MDS at different stages of the disease.
Previous studies have demonstrated that, under hypoxic conditions, [CD4.sup.+] cells preferentially differentiate into Th17 rather than Treg cells due to HIF1-[alpha] accumulation with subsequent transcriptional activation of Th17-associated ROR[gamma]t gene and promotion of proteasomal degradation of Foxp3 gene [10].
For Foxp3 staining, after washing cells with FACS buffer, the cells were processed using a Foxp3/transcription factor staining buffer set (eBioscience) according to the manufacturer's instructions.
All fluorochrome-conjugated antibodies (anti-human CD4 (RPA-T4), anti-human CD45RA (HI100), anti-human CD25 (BC96), anti-human FoxP3 (PCH101), anti-human IFN[gamma], anti-human IL-4, anti-human IL-17, and anti-mouse IL-6 were from eBioscience.
Treg cells, characterized by high expression of the transcription factor Foxp3, are considered to be important for maintaining self-tolerance and preventing autoimmune and inflammatory diseases by directly contacting effective immune cells; releasing suppressive cytokines, such as IL-10 and transforming growth factor(TGF-) and exhibiting their immunosuppressive effects on T cells [4-6].