Rapamycin Promotes Expansion of Functional CD4+CD25+FOXP3+ Regulatory T Cells of Both Healthy Subjects and Type 1 Diabetic Patients
Vita-Salute San Raffaele University · San Raffaele University of Rome · +4 more institutions
Abstract
CD4+CD25+FOXP3+ T regulatory cells (Tregs) are pivotal for the induction and maintenance of peripheral tolerance in both mice and humans. Rapamycin has been shown to promote tolerance in experimental models and to favor CD4+CD25+ Treg-dependent suppression. We recently reported that rapamycin allows in vitro expansion of murine CD4+CD25+FoxP3+ Tregs, which preserve their suppressive function. In the current study, we show that activation of human CD4+ T cells from healthy subjects in the presence of rapamycin leads to growth of CD4+CD25+FOXP3+ Tregs and to selective depletion of CD4+CD25- T effector cells, which are highly sensitive to the antiproliferative effect of the compound. The rapamycin-expanded Tregs…
Citation impact
- FWCI
- 13.27
- Percentile
- 100%
- References
- 42
Authors
6- MBManuela BattagliaCorresponding
Vita-Salute San Raffaele University, San Raffaele University of Rome, The San Raffaele Telethon Institute for Gene Therapy
- ASAngela Stabilini
The San Raffaele Telethon Institute for Gene Therapy
- BMBarbara Migliavacca
The San Raffaele Telethon Institute for Gene Therapy
- JHJutta Horejs‐Hoeck
University of Salzburg, Pädagogische Hochschule Salzburg
- TKThomas Kaupper
German Center for Diabetes Research
Topics & keywords
- FOXP3
- IL-2 receptor
- Effector
- Cell biology
- CD8
- Regulatory T cell
- Immunology
- Cancer research
- Good health and well-being