17 research outputs found
Additional file 1: of A multidimensional education program at substance dependence treatment centers improves patient knowledge and hepatitis C care
This file contains the English language version of the questionnaire used in the study. (PDF 51ย�kb
Additional file 2: of A multidimensional education program at substance dependence treatment centers improves patient knowledge and hepatitis C care
This file contains the raw data for the variables presented in this manuscript. (XLSX 238ย�kb
Correlations between CD25<sup>bright</sup>/CD4<sup>+</sup> aTreg frequencies and immunoblot band numbers.
<p>A–C: Bands recognized in immunoblots of HEp2-cytoplasmic proteins by SLE patients, unaffected relatives and unrelated control subjects. D–F: Bands recognized in immunoblots of HEp2-nuclear proteins. Regression lines represent linear regression.</p
Systematic gating for CD25<sup>bright</sup> aTregs.
<p>A. First, in order to specify the upper limit of CD25 staining in conventional T-cells for each sample, the ninety-ninth percentile of PE/Cy5 fluorescence intensity within CD4<sup>−</sup>CD45RO<sup>−</sup> cells (a population containing no Tregs) was determined as gate A. CD4<sup>+</sup>CD25<sup>bright</sup> aTregs in the same sample were then quantified as those CD4<sup>+</sup> cells that exceeded this value at least three-fold (gate B). B–D. The CD25<sup>bright</sup> gate (B) contains high proportions of Foxp3+ cells in samples from SLE patients, unaffected relatives and healthy control subjects. As exemplified by an active SLE patient (panel B), an unaffected relative (panel C) and a healthy control subject (panel D), the CD25<sup>bright</sup> gate B defined as 3xMFI(gate A) regularly contained 70–90% Foxp3+ cells within CD4+ lymphocytes when additional samples were stained for the same markers as previously but now in combination with intracellular Foxp3 staining.</p
Coreferentialities with CD25<sup>bright</sup>/CD4<sup>+</sup> frequencies.
*<p>Significance according to permutation test (see <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0033992#s4" target="_blank">methods</a>). Effects of bystander coreferentiality were checked for all significant tests (see <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0033992#s4" target="_blank">methods</a>), but rates of simulated bystander data reaching the respective test significance never exceeded 5%.</p
Group-wise coreferentialities between CD25<sup>bright</sup>/CD4+ aTreg frequencies and <i>IL2RA</i> genetic-effects model scores.
<p>A: SLE patients, B: unaffected relatives, C: unrelated controls. Reactivities to cytoplasmic bands are indicated by filled circles, anti-nuclear reactivities by triangles and anti-brain reactivities by crosses.</p
Correlations between aTreg frequencies (CD25<sup>bright</sup>/CD4<sup>+</sup>) and quantified SLE-associated specific autoreactive IgG.
<p>A–C: IgG anti-dsDNA. D–F: IgG anti-Sm. Regression lines represent linear regression.</p
Group-wise coreferentialities with aTreg frequencies, in respect to 130 IgG immunoblot reactivities as reference data.
<p>A–C: Coreferentiality between CD25<sup>bright</sup>/CD4<sup>+</sup> aTreg frequencies and IgG anti-HEp2-cytoplasmic immunoblot band numbers. D–F: Coreferentiality between aTreg frequencies and log-transformed IgG anti-Ro60/SSA. G–I: Coreferentiality between aTreg frequencies and log-transformed IgG anti-Sm. Reactivities to cytoplasmic bands are indicated by filled circles, anti-nuclear reactivities by triangles and anti-brain reactivities by crosses.</p
