It is possible that under different conditions CD8+CD28− T cells with regulatory properties are more prominent, and under these circumstances the use of MSC should be reconsidered. IL-15 is a cytokine that promotes CD8+CD28− T cell proliferation [30]. Interestingly, IL-15, next to IL-7, is crucial for the homeostatic maintenance of T cells in the absence of antigenic stimuli and expedites the loss of CD28 expression [49]. During normal exposure to antigen CD28 expression is transiently reduced but returns quickly to basal expression levels. Repeated NVP-BGJ398 chemical structure antigen exposure due to the natural ageing process, viral infections or viral reactivation

in immunocompromised patients causes a decline in CD28 expression, leading eventually to total loss of CD28. Surprisingly, we found that in our setting CD28+ T cells did not lose CD28 during allogeneic stimulation with PBMC, confirming that extended

rounds of antigen exposure are required to initiate reduction of CD28. Permanent decline of CD28 expression entails telomere AZD8055 nmr shortening and reduction of telomerase activity and is attributed to a defect in the CD28 promotor leading to transcriptional inactivation [50-54]. We, however, found that CD8+ T cells that were initially CD28− gained CD28 expression during allogeneic stimulation with PBMCs. Reinduction of CD28 expression in CD4+CD28− T cells is a known phenomenon and only possible until CD28− T cells have reached terminal differentiation. Warrington et al. described that combined stimulation of T cell receptor (TCR) and IL-12 receptor restored CD28 transcription and protein expression, Metalloexopeptidase while single stimulation of either the TCR or the IL-12 receptor was not sufficient [55]. IL-12 is produced by phagocytic cells, B cells and other antigen-presenting cells [56] and therefore potentially contributes to the CD28 re-expression in originally CD8+CD28− T cells in MLR. Although CD28 expression can be influenced up to a certain stage during T cell differentiation, MSC did not affect the immunophenotypical changes of CD8+CD28− T cells, nor did they cause loss of CD28 expression

in CD8+CD28+ T cells. Further, we found that MSC did not induce apoptosis in CD8+CD28− T cells, despite their ability to express Fas ligand (FasL) or to initiate the programmed death (PD)-1/PD-ligand 1 (PD-L1) pathway [57, 58]. These observations indicate that MSC solely have an anti-proliferative effect on CD8+CD28− T cells. Co-administration of MSC with other immunosuppressive drugs is not always encouraged; agents such as tacrolimus, mammalian target of rapamycin (mTor) inhibitor rapamycin and rabbit anti-thymocyte globulin (rATG) negatively affect the suppressive capacity of MSC in vitro [59-61]. At same time, MSC are able to reduce the efficacy of tacrolimus and rapamycin [59, 60]. As MSC lack expression of the CTLA-4 ligands CD80 and CD86, it was not surprising that belatacept did not diminish MSC function [62].