Abstract:
:The experimental autoimmune encephalomyelitis (EAE) model is indispensable for autoimmunity research, but model-specific T cell dynamics are sparsely studied. We used next-generation immunosequencing across lymphoid organs, blood and spinal cord in response to immunization with myelin basic protein (MBP) to study T cell repertoires and migration patterns. Surprisingly, most spinal cord T cells were unique to the individual animal despite the existence of shared MBP-specific clones, suggesting a previously underestimated T cell diversity. Almost complete emigration of pathogenic clones from blood to spinal cord indicates that blood is not a suitable compartment to study EAE-mediating T cells.
journal_name
J Neuroimmunoljournal_title
Journal of neuroimmunologyauthors
Schliffke S,Carambia A,Akyüz N,Thiele B,Herkel J,Binder Mdoi
10.1016/j.jneuroim.2019.03.014subject
Has Abstractpub_date
2019-07-15 00:00:00pages
49-56eissn
0165-5728issn
1872-8421pii
S0165-5728(18)30573-3journal_volume
332pub_type
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