Selective IL-2 responsiveness of regulatory T Cells through multiple intrinsic mechanisms supports the use of low-dose IL-2 therapy in type 1 diabetes

A. Yu; I. Snowhite; F. Vendrame; M. Rosenzwajg; D. Klatzman; A. Pugliese; T. R. Malek

doi:10.1089/dia.2016.2507

Selective IL-2 responsiveness of regulatory T Cells through multiple intrinsic mechanisms supports the use of low-dose IL-2 therapy in type 1 diabetes

A. Yu, I. Snowhite, F. Vendrame, M. Rosenzwajg, D. Klatzman, A. Pugliese, T. R. Malek

Research output: Contribution to journal › Comment/debate

Original language	English (US)
Pages (from-to)	S73
Journal	Diabetes Technology and Therapeutics
Volume	18
DOIs	https://doi.org/10.1089/dia.2016.2507
State	Published - Feb 2016

ASJC Scopus subject areas

Endocrinology, Diabetes and Metabolism
Endocrinology
Medical Laboratory Technology

Access to Document

10.1089/dia.2016.2507

Cite this

Yu, A., Snowhite, I., Vendrame, F., Rosenzwajg, M., Klatzman, D., Pugliese, A., & Malek, T. R. (2016). Selective IL-2 responsiveness of regulatory T Cells through multiple intrinsic mechanisms supports the use of low-dose IL-2 therapy in type 1 diabetes. Diabetes Technology and Therapeutics, 18, S73. https://doi.org/10.1089/dia.2016.2507

Selective IL-2 responsiveness of regulatory T Cells through multiple intrinsic mechanisms supports the use of low-dose IL-2 therapy in type 1 diabetes. / Yu, A.; Snowhite, I.; Vendrame, F.; Rosenzwajg, M.; Klatzman, D.; Pugliese, A.; Malek, T. R.

In: Diabetes Technology and Therapeutics, Vol. 18, 02.2016, p. S73.

Research output: Contribution to journal › Comment/debate

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