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Quantitative Measurement of Intrathecally Synthesized Proteins in Mice
Published on: November 29, 2019
Measles virus-specific plasma cells are prominent in subacute sclerosing panencephalitis CSF
G P Owens1, A M Ritchie, D H Gilden
1Department of Neurology, University of Colorado Health Sciences Center, Denver, CO 80262, USA. greg.owens@uchsc.edu
Objective:
To demonstrate the specificity of expanded CD138(+) plasma cell clones recovered from the CSF of a patient with subacute sclerosing panencephalitis (SSPE) for measles virus (MV).
Methods:
IgG variable region sequences of single-antibody-secreting CD138(+) cells sorted from SSPE CSF were amplified by single-cell PCR and analyzed. Human IgG1 recombinant antibodies (rAbs) were produced from four expanded CD138(+) clones and assayed for immunoreactivity against MV proteins.
Results:
Clonal expansion was a prominent feature of the SSPE plasma cell repertoire, and each of the four rAbs assayed was specific for either the MV fusion or the MV nucleocapsid protein.
Conclusions:
Expanded plasma cell clones in the CSF of patients with subacute sclerosing panencephalitis produce disease-relevant antibodies. Recombinant antibodies derived from CSF B cells could provide a tool to identify target antigens in idiopathic inflammatory disorders.
Insights
In subacute sclerosing panencephalitis (SSPE), expanded plasma cells in cerebrospinal fluid (CSF) generate measles virus (MV)-specific antibodies. These findings highlight CSF B cells as potential diagnostic tools for neurological disorders.
Area of Science:
- Immunology
- Virology
- Neuroscience
Background:
- Subacute sclerosing panencephalitis (SSPE) is a rare, progressive neurological disorder associated with measles virus (MV) infection.
- The role of specific B cell responses within the central nervous system (CNS) in SSPE pathogenesis remains incompletely understood.
Observation:
- Plasma cells, identified by CD138 expression, showed significant clonal expansion in the cerebrospinal fluid (CSF) of an SSPE patient.
- Single-cell PCR analysis of IgG variable regions from these CSF plasma cells was performed.
Findings:
- Four recombinant antibodies (rAbs) were generated from expanded CSF plasma cell clones.
- All four rAbs demonstrated specific immunoreactivity against either the measles virus fusion (MVF) protein or the measles virus nucleocapsid (MVN) protein.
Implications:
- Expanded plasma cell clones in the SSPE patient's CSF produce antibodies directly relevant to the disease.
- Recombinant antibodies derived from CSF B cells represent a potential tool for identifying target antigens in idiopathic inflammatory disorders, including neurological conditions.
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