Background: Experimental autoimmune encephalomyelitis (EAE) induced by self-myelin antigen is
a widely used in multiple sclerosis (MS) model for preclinical studies of new therapeutics and potential
pathogenesis. By comparison with rodent EAE models, EAE models in primates are more similar to MS. Some
groups have developed EAE models in primates by using common marmoset (Callithrix jacchus). However,
this model has some limitations. EAE in cynomolgus monkey (Macaque fasciculrais) could overcome these
Objectives: The main objective of this study was to establish an ideal EAE cynomolgus monkey model
resembling human MS by immunizing human myelin oligodendrocyte glycoprotein (MOG) protein.
Methods: In this study, six female cynomolgus monkeys were divided into two separate experiment groups and
one monkey as the control. EAE was induced in cynomolgus monkey by immunizing with the recombinant
human myelin oligodendrocyte glycoprotein extracellular domain (1-125) (rhMOG1-125) and a synthetic
peptide, representing peptide 34-56 of human myelin oligodendrocyte glycoprotein (MOG34-56) in complete
Freund's adjuvant (CFA) by subcutaneous multipoint immunization in the armpit and inguinal region and in
combination with intravenous injection of pertussis toxin, and subsequent booster immunizations with the same
dose of antigen in incomplete Freund's adjuvant (IFA) until the animals developed clinically significant EAE
(score≥2). The body weight, clinical scores, magnetic resonance imaging (MRI), histopathology, antibody,
cytokine profiling and antigen-specific lymphocyte proliferation were evaluated.
Results: The results showed that despite the different time intervals between onset and significant neurological
deficits, all the cynomolgus monkeys immunized with rhMOG1-125 or MOG34-56 developed clinically
significant acute fulminant or mild forms of EAE, with a success rate of 100%. The clinical courses were
obvious heterogeneity which closely resembles MS. MOG34-56 immunization was much milder compared with
rhMOG1-125 immunized individuals, at least in cynomolgus monkeys. Inflammation and demyelinated lesions
were present in the brains and spinal cords. Immune profiling revealed high IgG levels associated with early
onset of EAE but not the course of the disease. Significant antigen-specific T lymphocyte responses against
immunodominant epitopes of MOG were also detected.
Conclusion: Our results indicated rhMOG1-125 and MOG34-56 could induce successfully EAE models
resembling MS in cynomolgus monkeys. The synergistic action of anti-myelin T cells and Abs during the
pathogenesis of EAE could establish a more ideal EAE model.