Abstract:
:Multiple sclerosis (MS) is characterized by demyelinated and inflammatory lesions in the brain and spinal cord that are highly variable in terms of cellular content. Here, we used imaging mass cytometry (IMC) to enable the simultaneous imaging of 15+ proteins within staged MS lesions. To test the potential for IMC to discriminate between different types of lesions, we selected a case with severe rebound MS disease activity after natalizumab cessation. With post-acquisition analysis pipelines we were able to: (1) Discriminate demyelinating macrophages from the resident microglial pool; (2) Determine which types of lymphocytes reside closest to blood vessels; (3) Identify multiple subsets of T and B cells, and (4) Ascertain dynamics of T cell phenotypes vis-à-vis lesion type and location. We propose that IMC will enable a comprehensive analysis of single-cell phenotypes, their functional states and cell-cell interactions in relation to lesion morphometry and demyelinating activity in MS patients.
journal_name
Elifejournal_title
eLifeauthors
Ramaglia V,Sheikh-Mohamed S,Legg K,Park C,Rojas OL,Zandee S,Fu F,Ornatsky O,Swanson EC,Pitt D,Prat A,McKee TD,Gommerman JLdoi
10.7554/eLife.48051subject
Has Abstractpub_date
2019-08-01 00:00:00issn
2050-084Xpii
48051journal_volume
8pub_type
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