TY - JOUR
T1 - Glucose-sensitive insulin with attenuation of hypoglycaemia
AU - Hoeg-Jensen, Thomas
AU - Kruse, Thomas
AU - Brand, Christian L.
AU - Sturis, Jeppe
AU - Fledelius, Christian
AU - Nielsen, Peter K.
AU - Nishimura, Erica
AU - Madsen, Alice R.
AU - Lykke, Lennart
AU - Halskov, Kim S.
AU - Koščová, Simona
AU - Kotek, Vladislav
AU - Davis, Anthony P.
AU - Tromans, Robert A.
AU - Tomsett, Michael
AU - Peñuelas-Haro, Guillem
AU - Leonard, Daniel J.
AU - Orchard, Michael G.
AU - Chapman, Andy
AU - Invernizzi, Gaetano
AU - Johansson, Eva
AU - Granata, Daniele
AU - Hansen, Bo F.
AU - Pedersen, Thomas A.
AU - Kildegaard, Jonas
AU - Pedersen, Karen Margrethe
AU - Refsgaard, Hanne H.F.
AU - Alifrangis, Lene
AU - Fels, Johannes J.
AU - Neutzsky-Wulff, Anita V.
AU - Sauerberg, Per
AU - Slaaby, Rita
N1 - Publisher Copyright:
© The Author(s) 2024.
PY - 2024/10/24
Y1 - 2024/10/24
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=85206876822&partnerID=8YFLogxK
U2 - 10.1038/s41586-024-08042-3
DO - 10.1038/s41586-024-08042-3
M3 - Article (Academic Journal)
C2 - 39415004
AN - SCOPUS:85206876822
SN - 0028-0836
VL - 634
SP - 944
EP - 951
JO - Nature
JF - Nature
ER -