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      Temporal Biological variability in dendritic cells and regulatory T cells in peripheral blood of healthy adults

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          Abstract

          Background

          Studies evaluating circulating dendritic cells (DCs) and natural and induced regulatory T cells (nTregs, iTregs) are often obtained at a single time point and difficult to interpret without understanding their intrinsic day-to-day biologic variability.

          Methods

          We investigated the day-to-day variability in quantifying DCs, nTregs (FoxP3+CD25+CD4+) and cytokine production by iTregs (Granzyme B –GZB, Th1/2 cytokines following CD3 plus CD46 in vitro activation) from peripheral blood mononuclear cells (PBMC) collected on three consecutive days in healthy adults. Intraclass correlation coefficients (ICC) were used to evaluate intra-individual variability.

          Results

          In 10 healthy adults, the %PBMC of plasmacytoid (pDC) and myeloid (mDC1 and mDC2) were 0.27±0.12, 0.22±0.10, and 0.02±0.02, with ICC 0.91, 0.90, and 0.17 respectively. Natural Tregs (3.27±1.27% CD4+ cells) had an ICC of 0.86. Inducible Tregs (GZB-positive, 35.3±17.7% CD4+ cells) had an ICC of 0.77. The ICC for IL-10, TNF-α, IFN-γ, IL-4, and IL-5 production by iTregs were 0.49, 0.63, 0.68, 0.74, and 0.82, respectively. There were no significant changes in ICC (<0.1) after adjusting for age, gender and atopy except for IL-4. Substantial variability for iTregs was determined for the control condition (PBS with IL-2).

          Conclusions

          No meaningful day-to-day biologic variability was observed for the quantification of nTregs, pDC and mDC1 in normal adults; however, there was substantial variability in measuring mDC2 proportions and iTreg production of IL-10. These results suggest obtaining an average of several measurements over time to determine the most representative value of these biologic measures.

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          Author and article information

          Journal
          1305440
          4818
          J Immunol Methods
          J. Immunol. Methods
          Journal of immunological methods
          0022-1759
          1872-7905
          15 March 2016
          06 February 2016
          April 2016
          01 April 2017
          : 431
          : 63-65
          Affiliations
          [1 ]Division of Allergy, Immunology and Pulmonary Medicine, Department of Pediatrics, St. Louis Children’s Hospital, Washington University School of Medicine. Address: Campus box 8116, One Children’s Place St. Louis, Missouri, 63110, USA
          [2 ]Division of Pulmonary and Critical Care Medicine, Department of Internal Medicine, Washington University School of Medicine. Address: 660 S. Euclid Ave, Campus box 8052, St. Louis, MO, 63110, USA
          [3 ]Division of Biostatistics, Washington University School of Medicine. Address: 660 S. Euclid Ave, Campus box 8067, St. Louis, MO, 63110, USA
          Author notes
          Corresponding author: Mario Castro, MD, MPH, Division of Pulmonary and Critical Care Medicine, Department of Pediatrics, Washington University School of Medicine, 660 S. Euclid Ave, Campus Box, St. Louis, MO 63110 castrom@ 123456dom.wustl.edu Telephone number: +1-314-362-6904, Fax number: +1-314-362-2307
          Article
          PMC4801223 PMC4801223 4801223 nihpa760195
          10.1016/j.jim.2016.02.006
          4801223
          26859243
          d350945f-47b5-4549-baff-e873f69741be
          History
          Categories
          Article

          dendritic cells,regulatory T cells,variability,human
          dendritic cells, regulatory T cells, variability, human

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