Measles virus-polypeptide specificity of the cytotoxic T-lymphocyte response in multiple sclerosis

S Dhib-Jalbut1, D E McFarlin, H F McFarland

  • 1Neuroimmunology Branch, NINCDS, Bethesda, MD 20892.

Insights

Patients with multiple sclerosis (MS) exhibit a reduced measles virus (MV)-specific cytotoxic T-lymphocyte (CTL) response, particularly to HA and NC viral proteins. This defect is likely due to issues in CTL response induction or maintenance, not T-cell repertoire problems.

Area of Science:

  • Immunology
  • Neuroimmunology
  • Virology

Background:

  • Multiple sclerosis (MS) patients often show diminished measles virus (MV)-specific cytotoxic T-lymphocyte (CTL) generation.
  • The underlying mechanisms for this reduced CTL response in MS remain unclear.

Purpose of the Study:

  • To investigate the mechanisms behind the reduced MV-specific CTL response in MS patients.
  • To analyze the CTL response to specific MV polypeptides (hemagglutinin, fusion, nucleocapsid) in MS patients and healthy controls.

Main Methods:

  • Studied MV polypeptide-specific CTL responses in 14 MS patients and 8 healthy controls.
  • Utilized limiting dilution analysis to assess T-cell suppression.
  • Compared lymphoproliferative responses to MV antigens between MS patients and controls.

Main Results:

  • MS patients displayed a significant defect in CTL response to MV hemagglutinin (HA) and nucleocapsid (NC) polypeptides.
  • A lesser reduction in CTL response was observed for the MV fusion (F) polypeptide.
  • Suppression was ruled out as a cause for reduced CTL activity; T-cell repertoire and cross-reactivity with myelin antigens were also unlikely.
  • Lymphoproliferative responses were comparable between MS patients and controls.

Conclusions:

  • The reduced MV-specific CTL response in MS is not attributed to T-cell repertoire defects or myelin cross-reactivity.
  • Potential causes include abnormalities in the induction or maintenance of the MV-CTL response.
  • Sequestration of MV-reactive CTLs within the central nervous system (CNS) due to MV antigen recognition is a plausible mechanism.