Limitations of IL-2 and rapamycin in immunotherapy of type 1 diabetes

A Baeyens, L Pérol, G Fourcade, N Cagnard… - Diabetes, 2013 - Am Diabetes Assoc
A Baeyens, L Pérol, G Fourcade, N Cagnard, W Carpentier, J Woytschak, O Boyman
Diabetes, 2013Am Diabetes Assoc
Administration of low-dose interleukin-2 (IL-2) alone or combined with rapamycin (RAPA)
prevents hyperglycemia in NOD mice. Also, low-dose IL-2 cures recent-onset type 1
diabetes (T1D) in NOD mice, partially by boosting pancreatic regulatory T cells (Treg cells).
These approaches are currently being evaluated in humans. Our objective was to study the
effect of higher IL-2 doses (250,000–500,000 IU daily) as well as low-dose IL-2 (25,000 IU
daily) and RAPA (1 mg/kg daily)(RAPA/IL-2) combination. We show that, despite further …
Administration of low-dose interleukin-2 (IL-2) alone or combined with rapamycin (RAPA) prevents hyperglycemia in NOD mice. Also, low-dose IL-2 cures recent-onset type 1 diabetes (T1D) in NOD mice, partially by boosting pancreatic regulatory T cells (Treg cells). These approaches are currently being evaluated in humans. Our objective was to study the effect of higher IL-2 doses (250,000–500,000 IU daily) as well as low-dose IL-2 (25,000 IU daily) and RAPA (1 mg/kg daily) (RAPA/IL-2) combination. We show that, despite further boosting of Treg cells, high doses of IL-2 rapidly precipitated T1D in prediabetic female and male mice and increased myeloid cells in the pancreas. Also, we observed that RAPA counteracted IL-2 effects on Treg cells, failed to control IL-2–boosted NK cells, and broke IL-2–induced tolerance in a reversible way. Notably, the RAPA/IL-2 combination failure to cure T1D was associated with an unexpected deleterious effect on glucose homeostasis at multiple levels, including β-cell division, glucose tolerance, and liver glucose metabolism. Our data help to understand the therapeutic limitations of IL-2 alone or RAPA/IL-2 combination and could lead to the design of improved therapies for T1D.
Am Diabetes Assoc