Atypical antipsychotics in multiple sclerosis: A review of their in vivo immunomodulatory effects

Εleni Stamoula; Alexandra Ainatzoglou; Vasileios-Periklis Stamatellos; Ioannis Dardalas; Spyridon Siafis; Alkis Matsas; Konstantinos Stamoulas; Georgios Papazisis

doi:10.1016/j.msard.2022.103522

Atypical antipsychotics in multiple sclerosis: A review of their in vivo immunomodulatory effects

Mult Scler Relat Disord. 2022 Feb:58:103522. doi: 10.1016/j.msard.2022.103522. Epub 2022 Jan 12.

Authors

Εleni Stamoula¹, Alexandra Ainatzoglou², Vasileios-Periklis Stamatellos³, Ioannis Dardalas¹, Spyridon Siafis⁴, Alkis Matsas⁵, Konstantinos Stamoulas², Georgios Papazisis⁶

Affiliations

¹ Department of Clinical Pharmacology, School of Medicine, Aristotle University of Thessaloniki, Thessaloniki, Greece.
² School of Medicine, Aristotle University of Thessaloniki, Thessaloniki, Greece.
³ Department of Neurology, Klinik fur Neurologie, DRK Kliniken Berlin Kopenick, Berlin 12559, Germany.
⁴ Department of Clinical Pharmacology, School of Medicine, Aristotle University of Thessaloniki, Thessaloniki, Greece; Department of Psychiatry and Psychotherapy, School of Medicine, Technical University of Munich, Munich, Germany.
⁵ School of Medicine, National and Kapodistrian University of Athens, Greece.
⁶ Department of Clinical Pharmacology, School of Medicine, Aristotle University of Thessaloniki, Thessaloniki, Greece; Clinical Trials Unit, Special Unit for Biomedical Research and Education, School of Medicine, Aristotle University of Thessaloniki, Greece. Electronic address: papazisg@auth.gr.

PMID: 35063906
DOI: 10.1016/j.msard.2022.103522

Abstract

Introduction: The high efficacy of atypical antipsychotics (AAP) in treating diverse psychiatric disorders has been partly attributed to their capacity to curb neuroinflammation, a shared aspect of these diseases. These immunomodulatory properties of AAP have lately been explored in the context of multiple sclerosis (MS), an autoimmune demyelinating disease of the CNS.

Methods: This study aimed to review in vivo studies reporting on the therapeutic effects of AAP both in EAE, the main animal model of MS and in cuprizone-induced demyelination. For that matter we conducted a literature search and a screening process that eventually yielded 8 eligible studies.

Results: All studies agreed on the efficiency of AAP to dramatically reduce EAE severity and delay its onset, while suppressing the production of numerous inflammatory cytokines. Clozapine showcased similar yet more intense effects than risperidone, quetiapine and olanzapine, significantly attenuating CD4 T cell infiltration and myeloid cell activation, while upregulating Tregs. Clozapine also downregulated chemokines responsible for the migration of immune cells in the CNS and caused dopamine receptor levels in the brain of EAE mice to rise.

Discussion: Taken together, these findings unanimously attest to the anti-inflammatory and immunomodulatory properties of AAP, suggesting that their therapeutic potential expands beyond their current neuropsychiatric applications. Despite the salutary effects of AAP in MS reported in vivo, a clinical trial of clozapine on MS patients failed to confirm preclinical findings due to low acceptability of AAP and early participant withdrawal.

Conclusion: Although preclinical evidence unquestionably supports the multifaceted beneficial properties of AAP in MS, further investigation is required to elucidate the pharmacodynamic profile of these agents and allow for their proper clinical testing on MS patients.

Keywords: Antipsychotic; EAE; Immunomodulation; In vivo; MS; Neuroinflammation.

Publication types

Review

MeSH terms

Animals
Antipsychotic Agents* / pharmacology
Antipsychotic Agents* / therapeutic use
Clozapine* / pharmacology
Clozapine* / therapeutic use
Encephalomyelitis, Autoimmune, Experimental* / drug therapy
Humans
Mice
Multiple Sclerosis* / drug therapy
Olanzapine
Quetiapine Fumarate

Substances

Antipsychotic Agents
Quetiapine Fumarate
Clozapine
Olanzapine