Failure of antibody response to polysaccharide antigen in treated panhypopituitary adults

A. Mukherjee*, M. Helbert, W. D.J. Ryder, R. Borrow, J. R.E. Davis, S. M. Shalet

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

8 Citations (Scopus)

Abstract

Although pituitary hormones are known to affect immune function, treated hypopituitarism is not a recognized cause of immune deficiency in humans. We set out to assess integrity of baseline and stimulated immune function in severely hypopituitary adults. Twenty-one panhypopituitary adults (group 1), on stable pituitary replacement including growth hormone, and 12 healthy volunteers (group 2) were studied. Lymphocyte subsets, pneumococcal antibody levels pre- and 1 month after polysaccharide vaccination, T cell numbers and in-vitro interferon (IFN)-γ response were studied. There were no significant differences in T cell numbers or IFN-γ secretion. B cell numbers were lower in group 1, especially those with low prolactin levels. Independent of this finding, nine of 21 patients in this group had low antibody response to polysaccharide antigen. This was most striking in those with low insulin-like growth factor 1 levels and appeared to be independent of the use of anti-convulsants or corticosteroid replacement. Significant humoral immune deficiency is seen in panhypopituitarism and may contribute to morbidity.

Original languageEnglish
Pages (from-to)271-277
Number of pages7
JournalClinical and Experimental Immunology
Volume156
Issue number2
DOIs
Publication statusPublished - May 2009

Keywords

  • Autoimmunity
  • Hypopituitarism
  • Immune function
  • Prolactin deficiency

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