Experimental autoimmune meningitis: a novel neurological disease in CD28-deficient mice. Academic Article uri icon

Overview

abstract

  • C57BL/6 mice develop T-cell-mediated experimental autoimmune encephalomyelitis (EAE) after immunization with the neuroantigen myelin oligodendrocyte glycoprotein. (MOG). We immunized CD28-deficient C57BL/6 mice to determine the role of T cell costimulation in the immune response to MOG. CD28-/- mice developed experimental autoimmune meningitis (EAM). EAM is a fatal, acute disease characterized by simultaneous weakness in all limbs, photophobia, irritability, and spatial disorientation. Histologically, EAM consisted of an infiltrate of myeloid, monocytic, and lymphocytic leukocytes within the leptomeninges. In contrast, the brain parenchyma was unaffected. EAM was mediated by CD4+ T cells since CD4 depletion prevented the disease. Upon rechallenge, mice in which EAM was prevented by CD4+ cell depletion developed EAE not EAM. Therefore, the presence or absence of CD28 determines the initial phenotype of the immune response to MOG. EAM, which develops in the absence of CD28, is a unique experimental model for immune-mediated aseptic meningitis.

publication date

  • April 1, 1999

Research

keywords

  • Autoimmune Diseases
  • CD28 Antigens
  • Meningitis, Aseptic

Identity

Scopus Document Identifier

  • 0033109039

Digital Object Identifier (DOI)

  • 10.1006/clim.1998.4684

PubMed ID

  • 10219253

Additional Document Info

volume

  • 91

issue

  • 1