4.4 Review

Autoantibodies to central nervous system neuronal surface antigens: psychiatric symptoms and psychopharmacological implications

期刊

PSYCHOPHARMACOLOGY
卷 233, 期 9, 页码 1605-1621

出版社

SPRINGER
DOI: 10.1007/s00213-015-4156-y

关键词

Antibody; Immunoreactivity; Inflammation; Receptor; NMDAreceptor; Potassiumchannel; GABA receptor; Limbic system

资金

  1. Wellcome Trust [105758/Z/14/Z, 094849/Z/10/Z]
  2. Medical Research Council-UK [MCA-656-5QD30]
  3. Maudsley Charity [666]
  4. Astra-Zeneca
  5. Autifony
  6. BMS
  7. Eli Lilly
  8. Jansenn
  9. Lundbeck
  10. Lyden-Delta
  11. Otsuka
  12. Servier
  13. Sunovion
  14. Roche
  15. Wellcome Trust Intermediate Fellowship
  16. British Medical Association Vera Down Research Grant
  17. Hoffman la Roche
  18. National Institute for Health Research (NIHR) Biomedical Research Centre for Mental Health at South London and Maudsley NHS Foundation Trust and King's College London
  19. Medical Research Council [G0700995, 1116129, MC_U120097115] Funding Source: researchfish
  20. National Institute for Health Research [NF-SI-0510-10129] Funding Source: researchfish
  21. MRC [G0700995, MC_U120097115] Funding Source: UKRI
  22. Wellcome Trust [105758/Z/14/Z] Funding Source: Wellcome Trust

向作者/读者索取更多资源

Autoantibodies to central nervous system (CNS) neuronal surface antigens have been described in association with autoimmune encephalopathies which prominently feature psychiatric symptoms in addition to neurological symptoms. The potential role of these autoantibodies in primary psychiatric diseases such as schizophrenia or bipolar affective disorder is of increasing interest. We aimed to review the nature of psychiatric symptoms associated with neuronal surface autoantibodies, in the context of autoimmune encephalopathies as well as primary psychiatric disorders, and to review the mechanisms of action of these autoantibodies from a psychopharmacological perspective. The functional effects of the autoantibodies on their target antigens are described; their clinical expression is at least in part mediated by their effects on neuronal receptor function, primarily at the synapse, usually resulting in receptor hypofunction. The psychiatric effects of the antibodies are related to known functions of the receptor target or its complexed proteins, with reference to supportive genetic and pharmacological evidence where relevant. Evidence for a causal role of these autoantibodies in primary psychiatric disease is increasing but remains controversial; relevant methodological controversies are outlined. Non-receptor-based mechanisms of autoantibody action, including neuroinflammatory mechanisms, and therapeutic implications are discussed. An analysis of the autoantibodies from a psychopharmacological perspective, as endogenous, bioactive, highly specific, receptor-targeting molecules, provides a valuable opportunity to understand the neurobiological basis of associated psychiatric symptoms. Potentially, new treatment strategies will emerge from the improving understanding of antibody-antigen interaction within the CNS.

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