Secretory functions of three distinct Treg subsets To


Secretory functions of three distinct Treg subsets To

examine secretory function, sorted CD25++CD45RA+, CD25+++CD45RA-, or CD25++CD45RA- CD4+ T cells were stimulated with a cocktail of phorbol 12-myristate 13-acetate (PMA), ionomycin, and Golgi stop (brefeldin A and monensin) (eBioscience, San Diego, CA, USA) for 5 h. Then, intracytoplasmic expression of IL-2, IL-17, TNF-α, and IFN-γ were assessed using intracellular staining. Statistical analysis Statistical analysis was performed with the SPSS software (SPSS Standard version 13.0, IBM, Chicago, Tipifarnib IL, USA). The Mann–Whitney U-test or Kruskal–Wallis test was used for analyzing differences between data sets without normal distribution. Differences between independent data sets, with normal distribution, were analyzed using the Student’s t-test. Results Prevalence of three distinct Treg subsets

in the peripheral PLX4032 purchase circulation of 112 HNSCC patients Figure 1A illustrates the gating strategy used to identify the frequency of CD25+Foxp3+ Tregs in the total CD3+CD4+ T cells. The frequency of these Tregs in the peripheral circulation of HNSCC patients as a whole cohort was higher than in HD (8.12 ± 2.34% vs. 5.44 ± 1.92%, P < 0.0001) (Figure 1B), consistent with previous findings [10]. The frequency of three Treg subsets was then evaluated based on CD45RA and Foxp3 expression. The novelty of this study was that the frequency of CD45RA-Foxp3high Tregs (2.23 ± 0.98% vs. 0.77 ± 0.49%, P < 0.0001) and CD45RA-Foxp3lowCD4+ T cells (5.36 ± 1.63% vs. 3.70 ± 1.58%, P < 0.0001) in HNSCC patients was higher than in HD, whereas the frequency of CD45RA+Foxp3low Tregs in HNSCC patients was lower than in HD (0.53 ± 0.24% vs. 0.98 ± 0.61%, P < 0.0001) (Figure 1C,

Phosphoprotein phosphatase D). Acadesine cost Figure 1 Percentage of Treg subsets in 112 HNSCC patients. (A) Gating strategy used is illustrated. (B) Flow dot plots of Foxp3+CD25+ Tregs for one representative HD (left) and HNSCC patient (middle). Percentage (means ± SD) of Foxp3+CD25+ Tregs in HNSCC patients or HD (right). (C) Flow dot plots of each Treg subset (I: CD45RA+Foxp3low Tregs; II: CD45RA-Foxp3high Tregs; III: CD45RA-Foxp3lowCD4+ T cells) for one representative HD (left) and HNSCC patient (right). (D) Percentage (means ± SD) of each Treg subset in HNSCC patients or HD. HNSCC: head and neck squamous cell carcinoma. HD: healthy donors. Statistical comparisons were performed using the Mann–Whitney U-test. Suppressive and secretory function of three distinct Treg subsets The suppressive activity of each Treg subset from 12 randomly selected HNSCC patients was assessed by their ability to suppress the proliferation of autologous T cell populations (CD25-CD45RA+CD4+).

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