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A Long-Acting PYY 3-36 Analog Mediates Robust Anorectic Efficacy with Minimal Emesis in Nonhuman Primates.

Authors :
Rangwala SM
D'Aquino K
Zhang YM
Bader L
Edwards W
Zheng S
Eckardt A
Lacombe A
Pick R
Moreno V
Kang L
Jian W
Arnoult E
Case M
Jenkinson C
Chi E
Swanson RV
Kievit P
Grove K
Macielag M
Erion MD
SinhaRoy R
Leonard JN
Source :
Cell metabolism [Cell Metab] 2019 Apr 02; Vol. 29 (4), pp. 837-843.e5. Date of Electronic Publication: 2019 Feb 14.
Publication Year :
2019

Abstract

The gut hormone PYY <subscript>3-36</subscript> reduces food intake in humans and exhibits at least additive efficacy in combination with GLP-1. However, the utility of PYY analogs as anti-obesity agents has been severely limited by emesis and rapid proteolysis, a profile similarly observed with native PYY <subscript>3-36</subscript> in obese rhesus macaques. Here, we found that antibody conjugation of a cyclized PYY <subscript>3-36</subscript> analog achieved high NPY2R selectivity, unprecedented in vivo stability, and gradual infusion-like exposure. These properties permitted profound reduction of food intake when administered to macaques for 23 days without a single emetic event in any animal. Co-administration with the GLP-1 receptor agonist liraglutide for an additional 5 days further reduced food intake with only one animal experiencing a single bout of emesis. This antibody-conjugated PYY analog therefore may enable the long-sought potential of GLP-1/PYY-based combination treatment to achieve robust, well-tolerated weight reduction in obese patients.<br /> (Copyright © 2019 Elsevier Inc. All rights reserved.)

Details

Language :
English
ISSN :
1932-7420
Volume :
29
Issue :
4
Database :
MEDLINE
Journal :
Cell metabolism
Publication Type :
Academic Journal
Accession number :
30773465
Full Text :
https://doi.org/10.1016/j.cmet.2019.01.017