Author
Listed:
- Thomas Hoeg-Jensen
(Novo Nordisk)
- Thomas Kruse
(Novo Nordisk)
- Christian L. Brand
(Novo Nordisk)
- Jeppe Sturis
(Novo Nordisk)
- Christian Fledelius
(Novo Nordisk)
- Peter K. Nielsen
(Novo Nordisk)
- Erica Nishimura
(Novo Nordisk)
- Alice R. Madsen
(Novo Nordisk)
- Lennart Lykke
(Novo Nordisk)
- Kim S. Halskov
(Novo Nordisk)
- Simona Koščová
(APIGENEX)
- Vladislav Kotek
(APIGENEX)
- Anthony P. Davis
(University of Bristol)
- Robert A. Tromans
(Carbometrics)
- Michael Tomsett
(Carbometrics)
- Guillem Peñuelas-Haro
(Carbometrics)
- Daniel J. Leonard
(Carbometrics)
- Michael G. Orchard
(Carbometrics)
- Andy Chapman
(Carbometrics)
- Gaetano Invernizzi
(Novo Nordisk)
- Eva Johansson
(Novo Nordisk)
- Daniele Granata
(Novo Nordisk)
- Bo F. Hansen
(Novo Nordisk)
- Thomas A. Pedersen
(Novo Nordisk)
- Jonas Kildegaard
(Novo Nordisk)
- Karen-Margrethe Pedersen
(Novo Nordisk)
- Hanne H. F. Refsgaard
(Novo Nordisk)
- Lene Alifrangis
(Novo Nordisk)
- Johannes J. Fels
(Novo Nordisk)
- Anita V. Neutzsky-Wulff
(Novo Nordisk)
- Per Sauerberg
(Novo Nordisk)
- Rita Slaaby
(Novo Nordisk)
Abstract
The risk of inducing hypoglycaemia (low blood glucose) constitutes the main challenge associated with insulin therapy for diabetes1,2. Insulin doses must be adjusted to ensure that blood glucose values are within the normal range, but matching insulin doses to fluctuating glucose levels is difficult because even a slightly higher insulin dose than needed can lead to a hypoglycaemic incidence, which can be anything from uncomfortable to life-threatening. It has therefore been a long-standing goal to engineer a glucose-sensitive insulin that can auto-adjust its bioactivity in a reversible manner according to ambient glucose levels to ultimately achieve better glycaemic control while lowering the risk of hypoglycaemia3. Here we report the design and properties of NNC2215, an insulin conjugate with bioactivity that is reversibly responsive to a glucose range relevant for diabetes, as demonstrated in vitro and in vivo. NNC2215 was engineered by conjugating a glucose-binding macrocycle4 and a glucoside to insulin, thereby introducing a switch that can open and close in response to glucose and thereby equilibrate insulin between active and less-active conformations. The insulin receptor affinity for NNC2215 increased 3.2-fold when the glucose concentration was increased from 3 to 20 mM. In animal studies, the glucose-sensitive bioactivity of NNC2215 was demonstrated to lead to protection against hypoglycaemia while partially covering glucose excursions.
Suggested Citation
Thomas Hoeg-Jensen & Thomas Kruse & Christian L. Brand & Jeppe Sturis & Christian Fledelius & Peter K. Nielsen & Erica Nishimura & Alice R. Madsen & Lennart Lykke & Kim S. Halskov & Simona Koščová & V, 2024.
"Glucose-sensitive insulin with attenuation of hypoglycaemia,"
Nature, Nature, vol. 634(8035), pages 944-951, October.
Handle:
RePEc:nat:nature:v:634:y:2024:i:8035:d:10.1038_s41586-024-08042-3
DOI: 10.1038/s41586-024-08042-3
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