Identification of a Second Mimicry Epitope from Acanthamoeba castellanii that Induces CNS Autoimmunity by Generating Cross-Reactive T Cells for MBP 89–101 in SJL Mice

Authors

• Chandirasegaran Massilamany, University of Nebraska-LincolnFollow
• Oluwatoyin A. Asojo, University of Nebraska Medical CenterFollow
• Arunakumar Gangaplara, University of Nebraska - Lincoln
• David J. Steffen, University of Nebraska-LincolnFollow
• Jay Reddy, University of Nebraska - LincolnFollow

Document Type

Article

Date of this Version

2011

Citation

International Immunology (2011) 23(12): 729-739. DOI: 10.1093/intimm/dxr084.

Comments

Published for the Japanese Society for Immunology by Oxford University Press, 2011. Used by permission.

Abstract

We had previously reported that Acanthamoeba castellanii (ACA) contains a mimicry epitope for proteolipid protein 139–151 capable of inducing central nervous system (CNS) autoimmunity in SJL/J mice. We now present evidence that ACA also contains a mimicry epitope for myelin basic protein (MBP) 89–101, a derivative from amoebic nicotinamide adenine dinucleotide dehydrogenase subunit 2 (NAD). The epitope, NAD 108–120, contains a discontinuous stretch of six amino acids in the core region (VVFFKNIILIGFL) sharing 46% identity with MBP 89–101 (VHFFKNIVTPRTP; identical residues are underlined). SJL mice immunized with NAD 108–120 develop encephalomyelitis similar to the disease induced by the cognate peptide. We demonstrate that NAD 108–120 induces T cells that cross-react with MBP 89–101; the antigen-sensitized T cells, which produce predominantly T helper (T_h) 1 and T_h17 cytokines, transfer disease in naive SJL recipients reminiscent of the disease induced with MBP 89–101. This is the first report to demonstrate that a solitary microbe can induce CNS autoimmunity by generating cross-reactive T cells for multiple myelin antigens.