Myelin‐specific T cells in animals with Japanese macaque encephalomyelitis. Issue 2 (13th January 2021)

• Record Type: Journal Article
• Authors: Govindan, Aparna N.; Fitzpatrick, Kristin S.; Manoharan, Minsha; Tagge, Ian; Kohama, Steven G.; Ferguson, Betsy; Peterson, Samuel M.; Wong, Grayson S.; Rooney, William D.; Park, Byung; Axthelm, Michael K.; Bourdette, Dennis N.; Sherman, Larry S.; Wong, Scott W.
• Is Part Of: Annals of clinical and translational neurology. Volume 8:Issue 2(2021)
• Page Start: 456
• Page End: 470
• Publication Date: 2021-01-13
• Subjects: Nervous system -- Diseases -- Periodicals; Neurology -- Periodicals; 616.8005
• DOI: 10.1002/acn3.51303
• Languages: English
• ISSNs: 2328-9503

Abstract

Abstract: Objective: To determine whether animals with Japanese macaque encephalomyelitis (JME), a spontaneous demyelinating disease similar to multiple sclerosis (MS), harbor myelin‐specific T cells in their central nervous system (CNS) and periphery. Methods: Mononuclear cells (MNCs) from CNS lesions, cervical lymph nodes (LNs) and peripheral blood of Japanese macaques (JMs) with JME, and cervical LN and blood MNCs from healthy controls or animals with non‐JME conditions were analyzed for the presence of myelin‐specific T cells and changes in interleukin 17 (IL‐17) and interferon gamma (IFN γ ) expression. Results: Demyelinating JME lesions contained CD4 + T cells and CD8 + T cells specific to myelin oligodendrocyte glycoprotein (MOG), myelin basic protein (MBP), and/or proteolipid protein (PLP). CD8 + T‐cell responses were absent in JME peripheral blood, and in age‐ and sex‐matched controls. However, CD4 + Th1 and Th17 responses were detected in JME peripheral blood versus controls. Cervical LN MNCs from eight of nine JME animals had CD3 + T cells specific for MOG, MBP, and PLP that were not detected in controls. Mapping myelin epitopes revealed a heterogeneity in responses among JME animals. Comparison of myelin antigen sequences with those of JM rhadinovirus (JMRV), which is found in JME lesions, identified six viral open reading frames (ORFs) with similarities to myelin antigen sequences. Overlapping peptides to these JMRV ORFs did not induce IFN γ responses. Interpretations: JME possesses an immune‐mediated component that involves both CD4 + and CD8 + T cells specific for myelin antigens. JME may shed new light on inflammatory demyelinating disease pathogenesis linked to gamma‐herpesvirus infection.