Hostname: page-component-7c8c6479df-ws8qp Total loading time: 0 Render date: 2024-03-28T17:49:02.293Z Has data issue: false hasContentIssue false

Interferons, serotonin and neurotoxicity

Published online by Cambridge University Press:  01 March 2000

DAVID B. MENKES
Affiliation:
Dunedin School of Medicine, University of Otago and Dunedin Hospital, Dunedin, New Zealand
JAMES A. MacDONALD
Affiliation:
Dunedin School of Medicine, University of Otago and Dunedin Hospital, Dunedin, New Zealand

Abstract

Background. Interferons are a class of cytokines profoundly affecting immune function. Several interferons are now synthesized and used clinically, notably for viral diseases and cancer. In addition to their desired immune effects, interferons cause a number of toxicities, including prominent effects on the nervous system.

Methods. This literature review focused on the incidence of depression associated with interferon treatment. Possible neurochemical mechanisms and remedial strategies were also considered.

Results. Interferon treatment, particularly with the alpha subtype, is unquestionably linked with depression, but the strength of association is uncertain because of erratic ascertainment and pre- treatment co-morbidity. A likely pathogenic mechanism has been described, involving interferon suppression of serotonin synthesis. Controlled treatment trials of interferon-induced depression are not yet available.

Conclusions. Neurotoxicity substantially limits the use of interferons. At least some of the risk of depression appears to derive from their anti-serotonergic effects, consistent with the large body of evidence pointing to a general link between serotonin and affective illness. Vigilant detection and aggressive treatment of depression is necessary to optimize interferon treatment of many patients.

Type
REVIEW ARTICLE
Copyright
© 2000 Cambridge University Press

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)