Biological measures and cellular immunological function in depressed psychiatric inpatients

E M Levy1, D J Borrelli, S M Mirin

  • 1Department of Microbiology, Boston University School of Medicine, MA 02118-2394.

Psychiatry Research
|February 1, 1991
PubMed

Insights

Major depression is linked to reduced cellular immune function, specifically lower concanavalin A (con A) response. Antihistamine use may also negatively impact immune function in depressed patients.

Area of Science:

  • Immunology
  • Psychiatry
  • Cellular Biology

Background:

  • Depression is a complex disorder with potential links to immune system dysregulation.
  • Previous research suggests alterations in cellular immunity in individuals with depressive disorders.

Purpose of the Study:

  • To investigate cellular immune function in psychiatric inpatients diagnosed with major depression compared to controls.
  • To explore differences in immune response between major depression and other depressive subtypes.

Main Methods:

  • Assessed mitogen responsiveness (concanavalin A, phytohemagglutinin, pokeweed mitogen), natural killer cell activity, and T cell subsets (CD4, CD8).
  • Included physically healthy subjects with a minimum 14-day washout period for psychoactive medications.
  • Utilized paired comparisons for patients with major depression versus controls.

Main Results:

  • Patients with major depression showed a statistically significant reduction in concanavalin A (con A) response compared to controls.
  • Major depression patients exhibited significantly lower con A and phytohemagglutinin (PHA) responses than patients with other depressive forms.
  • Antihistamine use was unexpectedly associated with lower immune function.

Conclusions:

  • Major depression is associated with impaired cellular immune function, particularly T-cell mitogen responses.
  • Specific immune deficits may differentiate major depression from other depressive disorders.
  • Further research is warranted to understand the impact of antihistamine use on immune function in depression.