T cell response to Hu-D peptides in patients with anti-Hu syndrome

J Neurooncol. 2005 Feb;71(3):231-6. doi: 10.1007/s11060-004-1723-1.

Abstract

The anti-Hu syndrome is the most common paraneoplastic neurologic syndrome but the exact mechanism of immune mediated neuronal injury remains unknown. Anti-Hu antibodies do not appear to play a pivotal role in the pathogenesis of the disease. To assess cell-mediated immunity, we selected 51 peptides from the Hu-D sequence and tested their ability to bind to six common HLA class I molecules. Stable complexes with purified HLA molecules were obtained with 19/51 (37%) selected peptides. Subsequently, the ability of the 19 HLA-binding peptides to stimulate T cells from 10 patients and 10 control subjects was evaluated by detecting IFN-gamma secretion. An anti-peptide T-cell response was observed in 7/10 Hu-positive patients but also in 3/10 control subjects. Overall, a significant T-cell activation occurred in response to 74% (14 out of 19) of the selected peptides in the Hu-positive patients vs. 16% (3 out of 19) in the control group (p < 0.001). In addition, T cells of patients tested within 3 months of the onset of anti-Hu syndrome responded to 82% (14 out of 17) of assessed Hu-D peptides vs. 37% (7 out of 19) in patients tested 1 year or more after developing the syndrome (p < 0.01). Thus, the present study suggests a role of cellular immunity during the course of anti-Hu syndrome.

Publication types

  • Clinical Trial
  • Controlled Clinical Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Carcinoma, Small Cell / complications
  • Carcinoma, Small Cell / immunology*
  • Cells, Cultured
  • ELAV Proteins
  • HLA-A Antigens / immunology
  • HLA-A Antigens / metabolism
  • Humans
  • Immunity, Cellular / immunology*
  • Interferon-gamma / metabolism
  • Nerve Tissue Proteins / immunology*
  • Nerve Tissue Proteins / metabolism
  • Paraneoplastic Syndromes, Nervous System / complications
  • Paraneoplastic Syndromes, Nervous System / immunology*
  • Peptide Fragments / immunology
  • RNA-Binding Proteins / immunology*
  • RNA-Binding Proteins / metabolism
  • Statistics, Nonparametric
  • Syndrome
  • T-Lymphocytes / immunology*
  • T-Lymphocytes / metabolism

Substances

  • ELAV Proteins
  • HLA-A Antigens
  • Nerve Tissue Proteins
  • Peptide Fragments
  • RNA-Binding Proteins
  • Interferon-gamma