Unique B cell responses in B cell-dependent and B cell-independent EAE

Abstract

Previous studies characterized B cell-dependent and B cell-independent models of experimental autoimmune encephalomyelitis (EAE) in C57BL/6 mice. To further characterize the B cell response generated in these two models, the serum antibody response and the B cell surface immunoglobulin (Ig) repertoire were analyzed following immunization of wild-type C57BL/6 mice with either recombinant myelin oligodendrocyte glycoprotein (MOG; B cell-dependent EAE) or the encephalitogenic MOG_35-55 peptide (B cell-independent EAE). Plasma ELISA revealed responses to unique linear epitopes of MOG following immunization with recombinant MOG that were absent in MOG_35-55-immunized animals. B cell repertoire analysis by RT-PCR identified a unique response restricted to 7183 Ig heavy chain variable gene family in mice immunized with recombinant MOG that was not observed in MOG_35-55-immunized mice. These insights could aid in the identification of the relevant B cell populations important to the pathogenesis of B cell-dependent EAE and in the mechanisms by which these B cell populations contribute to disease.

Keywords::

• Experimental autoimmune encephalomyelitis
• B cells
• antibody
• myelin oligodendrocyte glycoprotein
• B cell repertoire

Acknowledgements

The authors thank Dr Dean Nardelli and Dr Janis Eells for critical reading of the manuscript. This work was supported by a Graduate School Research Committee Award (UWM; JAL) and a Student Research Grant (UWM; GL).

Declaration of Interest: The authors report no conflicts of interest. The authors alone are responsible for the content and writing of the paper.