Cited by 72Adipokines, Inflammation, and Metabolic DiseasesRegulation of Appetite and ObesityPharmacology and Obesity Treatment

Immunogenicity associated with metreleptin treatment in patients with obesity or lipodystrophy

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Chan, Jean L., Koda, Joy, Heilig, Joseph S., Cochran, Elaine K., Gorden, Phillip, Oral, Elif A., Brown, Rebecca J.·2016·Clinical Endocrinology

Abstract

Summary: Objective: Recombinant human leptin (metreleptin) improves glycaemia and hypertriglyceridaemia in patients with generalized lipodystrophy; antibody development with in vitro neutralizing activity has been reported. We aimed to characterize antimetreleptin antibody development, including in vitro neutralizing activity. Design: Two randomized controlled studies in patients with obesity (twice‐daily metreleptin ± pramlintide for 20–52 weeks; 2006–2009); two long‐term, open‐label studies in patients with lipodystrophy (once‐daily or twice‐daily metreleptin for 2 months to 12·3 years; 2000–2014). Patients: A total of 579 metreleptin‐treated patients with obesity and 134 metreleptin‐treated patients with lipodystrophy (antibody/neutralizing activity data: n = 105). Measurements: Antimetreleptin antibodies, in vitro neutralizing activity. Results: Antimetreleptin antibodies developed in most patients (obese: 96–100%; lipodystrophy: 86–92%). Peak antibody titers (approximately 1:125 to 1:3125) generally occurred within 4–6 months and decreased with continued therapy (lipodystrophy). Antibody development did not adversely impact efficacy or safety (patients with obesity), except for inflammatory injection site reactions, but was associated with elevated leptin concentrations. Three patients with obesity developed in vitro neutralizing activity coincident with weight gain. Weight later returned to baseline in one patient despite persistent neutralizing activity. Four patients with generalized lipodystrophy developed in vitro neutralizing activity concurrent with worsened metabolic control; two with confounding comorbidities had sepsis. One patient with lipodystrophy had resolution of neutralizing activity on metreleptin. Conclusions: Development of in vitro neutralizing activity could be associated with loss of efficacy but has not been consistently associated with adverse clinical consequences. Whether neutralization of endogenous leptin with clinical consequences occurs remains unclear.

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Authors
Chan, J. L., Koda, J., Heilig, J. S., Cochran, E. K., Gorden, P., Oral, E. A., & Brown, R. J.
Affiliations
  • Bristol-Myers Squibb (United States) (US)
  • AstraZeneca San Diego CA USA
  • National Institutes of Health (US)
  • National Institute of Diabetes and Digestive and Kidney Diseases National Institutes of Health Bethesda MD USA
  • University of Michigan (US)
Corresponding author
Brown, Rebecca J.
Venue
Clinical Endocrinology
Publisher
Wiley
Published
2016-02-02
Volume
85
Issue
1
Pages
137-149
ISSN
  • 0300-0664 (ISSN-L)
  • 1365-2265
OpenAlex
W2244529015
Cited by
72
References
25
Citations by year
2026: 6 · 2025: 11 · 2024: 9 · 2023: 9 · 2022: 5 · 2021: 9 · 2020: 5 · 2019: 6 · 2018: 6 · 2017: 3 · 2016: 3
FWCI
3.14
Type
journal article
Language
en
Open access
Locations
  • Clinical Endocrinology (publishedVersion)
  • PubMed (publishedVersion)
  • PubMed Central (acceptedVersion)
Funders
  • AstraZeneca
  • Bristol-Myers Squibb
  • Amylin Pharmaceuticals
  • National Institutes of Health (UL1TR000433)
Topics
  • Health Sciences › Medicine › Epidemiology › Adipokines, Inflammation, and Metabolic Diseases
  • Life Sciences › Neuroscience › Endocrine and Autonomic Systems › Regulation of Appetite and Obesity
  • Health Sciences › Medicine › Pharmacology › Pharmacology and Obesity Treatment
Keywords
metreleptin, recombinant human leptin, immunogenicity, neutralizing antibodies, generalized lipodystrophy, obesity, pramlintide, hypertriglyceridemia, glycemic control, weight gain, injection site reactions, sepsis
MeSH terms
Adolescent, Adult, Antibodies, Antibody Formation, Child, Female, Humans, Lipodystrophy, Male, Middle Aged, Obesity, Leptin, Immunogenetic Phenomena, Young Adult, Islet Amyloid Polypeptide

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