Anti-ghrelin antibodies in appetite suppression: recent advances in obesity pharmacotherapy

Velimir Altabas1, Vanja Zjačić-Rotkvić1

  • 1Department of Endocrinology, Diabetes and Metabolic Diseases, "Mladen Sekso", Clinic for Internal Medicine, University Hospital Center "Sestre milosrdnice", Zagreb, Croatia.

Insights

Obesity is a growing global health crisis. While anti-ghrelin vaccines show promise in stimulating immune responses, current clinical trials have not yet demonstrated significant weight loss, requiring further research.

Area of Science:

  • Endocrinology and Metabolism
  • Immunology
  • Pharmacology

Background:

  • Obesity, characterized by excess body fat, is a major global health issue with significant negative impacts on life expectancy.
  • Ghrelin, an orexigenic neuropeptide primarily produced by the stomach, plays a key role in appetite regulation and fat storage.
  • Targeting ghrelin activity is a potential therapeutic strategy for obesity treatment by blocking its appetite-stimulating and fat-promoting effects.

Purpose of the Study:

  • To explore the potential of therapeutic vaccines as a novel approach for obesity treatment.
  • To review the development and efficacy of anti-ghrelin vaccines in preclinical and clinical settings.

Main Methods:

  • Development of various anti-ghrelin vaccine strategies to elicit an immune response against ghrelin.
  • Assessment of immune responses, specifically the generation of anti-ghrelin antibodies.
  • Evaluation of vaccine efficacy in a clinical trial setting, focusing on weight loss outcomes.

Main Results:

  • Several anti-ghrelin vaccines have successfully induced significant immune responses, evidenced by increased anti-ghrelin antibody levels in preclinical studies.
  • The sole clinical trial conducted to date yielded disappointing results, showing no statistically significant additional weight loss in the vaccinated group compared to controls.
  • Proof-of-concept has been established for anti-ghrelin vaccines, but further research is needed.

Conclusions:

  • Anti-ghrelin vaccines represent a potential new avenue for obesity pharmacotherapy, demonstrating the ability to generate specific immune responses.
  • Despite promising preclinical data, the clinical effectiveness of current anti-ghrelin vaccines for weight loss remains unproven.
  • Continued research and development are essential to create effective prophylactic and therapeutic vaccines for obesity prevention and treatment.

Related Concept Videos

Regulation of Food Intake01:30

Regulation of Food Intake

Short-term regulation of food intake primarily involves neural signals from the gastrointestinal (GI) tract, blood nutrient levels, and GI tract hormones. Communication between the gut and brain via vagal nerve fibers plays a significant role in evaluating the contents of the gut. Clinical studies have shown that protein ingestion produces a more prolonged response in these nerve fibers compared to an equivalent amount of glucose. Additionally, the activation of stretch receptors caused by GI...
3.1K
Glucagon-like Receptor Agonists01:24

Glucagon-like Receptor Agonists

Incretins include glucagon-like peptide-1 (GLP-1) and glucose-dependent insulinotropic polypeptide (GIP), which stimulate insulin secretion post-meals. In type 2 diabetes, GIP's efficacy is reduced, making GLP-1 a viable drug target. GIP originates from preproGIP.
GLP-1, when administered in high doses intravenously, triggers insulin secretion, inhibits glucagon release, slows gastric emptying, reduces food intake, and restores normal insulin secretion. However, its rapid inactivation by...
1.2K
Pharmacokinetics in Obese Patients: Drug Absorption and Distribution01:25

Pharmacokinetics in Obese Patients: Drug Absorption and Distribution

Obesity significantly alters the pharmacokinetic processes of drug absorption and distribution, presenting unique challenges in medical treatment. The increased fat tissue and decreased lean muscle in obese individuals can significantly affect how drugs are absorbed into the body and distributed across different tissues. This alteration can lead to variances in the effectiveness and safety of medications, necessitating adjustments in dosing or drug selection for obese patients.One notable...
351
Hypoglycemia and Glucagon01:15

Hypoglycemia and Glucagon

Without prolonged fasting, healthy individuals maintain blood glucose levels above 3.5 mM due to a well-adapted neuroendocrine counterregulatory system that effectively prevents acute hypoglycemia, a potentially life-threatening condition. The primary clinical scenarios for hypoglycemia encompass diabetes treatment, inappropriate production of endogenous insulin or insulin-like substances by tumors, and the use of glucose-lowering agents in non-diabetic individuals. Notably, hypoglycemia in the...
1.2K
Drugs Affecting GI Tract Motility: Serotonin Receptor Agonists01:23

Drugs Affecting GI Tract Motility: Serotonin Receptor Agonists

Serotonin, a crucial neurotransmitter synthesized by enterochromaffin cells, plays a cardinal role in regulating gastrointestinal (GI) motility. With over 90% of the body's total serotonin in the GI tract, its influence on digestive processes is profound. Serotonin is swiftly released upon various stimuli, such as food boluses or certain drugs, triggering intrinsic sensory neurons in the myenteric plexus and extrinsic vagal and spinal sensory neurons. This leads to the activation of the...
1.2K
Oral Hypoglycemic Agents: Glinides01:06

Oral Hypoglycemic Agents: Glinides

Repaglinide (Prandin) and Nateglinide (Starlix), known as glinides, are oral insulin secretagogues that stimulate insulin release from pancreatic β cells by closing the ATP-sensitive potassium channels (KATP channel). Repaglinide controls insulin release from pancreatic β cells by managing potassium efflux. It shares two binding sites with sulfonylureas and also has a unique site, indicating overlapping mechanisms of action. With a rapid onset and a 4-7 hour duration, it effectively...
837