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Sci Transl Med ; 6(248): 248ra106, 2014 Aug 06.
Article in English | MEDLINE | ID: mdl-25100740

ABSTRACT

In multiple sclerosis (MS), lymphocyte--in particular B cell--transit between the central nervous system (CNS) and periphery may contribute to the maintenance of active disease. Clonally related B cells exist in the cerebrospinal fluid (CSF) and peripheral blood (PB) of MS patients; however, it remains unclear which subpopulations of the highly diverse peripheral B cell compartment share antigen specificity with intrathecal B cell repertoires and whether their antigen stimulation occurs on both sides of the blood-brain barrier. To address these questions, we combined flow cytometric sorting of PB B cell subsets with deep immune repertoire sequencing of CSF and PB B cells. Immunoglobulin (IgM and IgG) heavy chain variable (VH) region repertoires of five PB B cell subsets from MS patients were compared with their CSF Ig-VH transcriptomes. In six of eight patients, we identified peripheral CD27(+)IgD(-) memory B cells, CD27(hi)CD38(hi) plasma cells/plasmablasts, or CD27(-)IgD(-) B cells that had an immune connection to the CNS compartment. Pinpointing Ig class-switched B cells as key component of the immune axis thought to contribute to ongoing MS disease activity strengthens the rationale of current B cell-targeting therapeutic strategies and may lead to more targeted approaches.


Subject(s)
B-Lymphocytes/immunology , Central Nervous System/pathology , Immune System/immunology , Immunoglobulin Class Switching , Multiple Sclerosis/blood , Multiple Sclerosis/immunology , Adult , Antibody Affinity/immunology , Cell Aggregation , Cerebrospinal Fluid/metabolism , Female , Flow Cytometry , Humans , Immunoglobulin Variable Region/immunology , Leukocytes, Mononuclear/metabolism , Male , Middle Aged , Multiple Sclerosis/pathology , Sequence Analysis, Protein , Somatic Hypermutation, Immunoglobulin/genetics , Young Adult
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