Erratum to: Age, atherosclerosis and type 2 diabetes reduce human mesenchymal stromal cell-mediated T-cell suppression
Stem Cell Research & Therapyvolume 8, Article number: 35 (2017)
The original article was published in Stem Cell Research & Therapy 2015 6:140
The original article  contains a mistakenly shortened abstract due to a misinterpretation during its production.
As such, the full abstract should read as follows:
Atherosclerosis is an age-associated, multifactorial process driven by immune activation and inflammation. Ongoing clinical trials aim to establish the role of mesenchymal stromal cells (MSCs) as therapeutic agents in atherosclerosis. The beneficial effects of MSCs derive from their immune-modulatory properties. Understanding the impact of aging and age-associated conditions (i.e., type 2 diabetes mellitus and atherosclerosis) on MSC function is key to maximizing their therapeutic potency. The aim of this study was to assess the effect of chronological and biological aging on human MSC-mediated CD4+ T-cell suppression. To this end human MSCs were isolated from adipose tissue and the MSC:CD4+ T-cell suppression was assessed in a co-culture system. MSCs from elderly donors (≥65 years) had significantly lower T-cell suppressive capacity compared to those from donors <65 years (p = 0.003). Furthermore, MSCs from patients with atherosclerosis and type 2 diabetes mellitus were less efficient at suppressing T-cell proliferation (atherosclerosis, p = 0.02; type 2 diabetes mellitus, p = 0.04; compared to non-disease controls). Sex and tobacco use did not impact the immunosuppressive capacity of MSCs. In summary, this study demonstrates that advanced age, atherosclerosis and type 2 diabetes mellitus reduce the functional potency of MSCs. Optimizing the criteria for the selection of MSC donors could enhance the results of cell-based therapies.
Kizilay M, et al. Age, atherosclerosis and type 2 diabetes reduce human mesenchymal stromal cell-mediated T-cell suppression. Stem Cell Res Ther. 2015;6:140.
The online version of the original article can be found under doi:10.1186/s13287-015-0127-9.