It would have been elegant and of great importance,

to be able to show functional data of the expanded CD4+CD25+CD127lo/− Tregs to establish the efficaciousness of the method and the possibility to use the expanded cells as Tregs, in future applications. Unfortunately, due to limited sample sizes, we were not able to show such results. Our study displayed a lower percentage of Tregs (CD4+CD25+CD127lo/−) among the CD4+ cells in T1D children. This is in line with studies describing reduced numbers of, or possibly functionally weak, CD4+CD25hi Tregs in diseased individuals bearing autoimmune disorders www.selleckchem.com/products/AZD2281(Olaparib).html such as T1D, multiple sclerosis and autoimmune polyglandular syndrome II

[28], [29] and [30]. This suggests that Tregs could be part of the explanation of the failed ability to maintain local self-tolerance during T1D development. However, to make the picture more complex, there are also studies that fail to present such differences for T1D patients [11] and [31]. One possible explanation for the lack of consensus for Tregs in T1D, and other disorders, could be the various ways of characterizing the cell type and defining the questions we ask on the impact of these cells. In studies where Tregs are defined as CD4+CD25hi, a certain spectrum of cells will be included in the calculations, compared to studies further adding FOXP3 and/or CD127 expression to the definition. Given that different ways of describing the see more cell type are used, part of the explanation for dissimilar findings could be as simple as diverse definition of Tregs. Moreover, it is conceivable that part of the explanation

may be the diverse paths taken in the quest to obtain the truth. While we are describing a lower fraction of Tregs in T1D as a lower percentage of CD4+CD25+CD127lo/− cells in the CD4+ T-cell population, Liu et al. [11] addresses the question as FOXP3 expression in the CD4+CD25+CD127lo/−, CD4+CD25−CD127lo/−, CD4+CD25+CD127+ and CD4+CD25−CD127+ Amino acid T-cell subsets. In addition to a lower proportion of CD4+CD25+CD127lo/− cells in the total CD4+ population, we also found that the relationship of CD4+CD25+CD127lo/− cells to CD4+CD25− cells to be lower in T1D, confirming the low Treg (CD4+CD25+CD127lo/−) proportion seen in the total CD4+ population. This skewed ratio, as compared with the healthy individuals, may be explained by an elevated proportion of CD4+CD25− cells accompanying T1D and further strengthens the findings of a lower proportion of CD4+CD25+CD127lo/− Tregs. The CD4+CD25− T-cells were recently described as a composition of responder cells with a lower proliferation rate and slower IL-2 response to in vitro stimulation, compared to already in vivo activated CD4+ responder T-cells expressing low amounts of CD25 [32].