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Updated: May 23, 2026

Using the Activity-based Anorexia Rodent Model to Study the Neurobiological Basis of Anorexia Nervosa
Published on: October 22, 2015
Anorexia nervosa, autoimmunity and the hygiene hypothesis
Meghan J Acres1, Joseph J Heath, James A Morris
1Faculty of Health and Medicine, Lancaster University, Lancaster LA1 4YW, United Kingdom.
Anorexia nervosa may be an autoimmune disease triggered by microbes, leading to auto-antibodies that disrupt appetite regulation. Further research and immunoglobulin therapy trials are suggested for this complex eating disorder.
Area of Science:
- Immunology
- Neuroscience
- Psychiatry
Background:
- Anorexia nervosa (AN) is increasingly prevalent, particularly in females, with epidemiological patterns suggesting environmental influences.
- Existing research indicates the presence of auto-antibodies to regulatory peptides in AN patients, potentially linked to microbial antigens.
Purpose of the Study:
- To investigate the hypothesis that anorexia nervosa is an autoimmune disorder resulting from microbial exposure.
- To explore the role of auto-antibodies and their correlation with disease psychopathology.
Main Methods:
- Serological analysis for IgG, IgA, and IgM auto-antibodies against regulatory peptides and hypothalamic neurons.
- Comparison of auto-antibody levels in AN patients, bulimia nervosa patients, and healthy controls.
- Epidemiological data analysis, including incidence, demographics, and seasonal birth variations.
Main Results:
- Auto-antibodies to appetite and mood regulatory peptides, showing homology with microbial sequences, are present in AN patients.
- Auto-antibodies to alpha-melanocyte stimulating hormone (αMSH) correlate with AN psychopathology.
- Similar auto-antibodies are found in bulimia nervosa patients and controls, necessitating further investigation.
Conclusions:
- Epidemiological and serological findings support the autoimmune hypothesis for AN, aligning with the hygiene hypothesis.
- Further research, including large case-control studies and MHC gene polymorphism assessment, is warranted.
- Pooled immunoglobulin therapy may be a viable treatment option for severe, life-threatening AN cases.
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