Journal of neuroimmunology · 2012
Key role of CXCL13/CXCR5 axis for cerebrospinal fluid B cell recruitment in pediatric OMS.
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Pranzatelli Michael R, Tate Elizabeth D, McGee Nathan R, Travelstead Anna L, Ransohoff Richard M, Ness Jayne M, Colliver Jerry A
Аннотация
To study aberrant B cell trafficking into the CSF in opsoclonus-myoclonus syndrome (OMS), chemoattractants CXCL13 and CXCL12, and B cell frequency and CXCR5 expression, were evaluated. CSF CXCL13 concentration and the CSF/serum ratio were higher in untreated OMS than controls, related directly to OMS severity and inversely to OMS duration, and correlated with CSF B cell frequency and oligoclonal bands. CXCL12 showed the opposite pattern. Selective accumulation of CXCR5+ memory B cells in CSF was found. In ACTH-treated OMS, CXCL13, but not CXCL12, was lower. These data implicate the chemokine/chemoreceptor pair CXCL13/CXR5 in B cell recruitment to the CNS in OMS. CXCL13 and CXCL12 may serve as reciprocal biomarkers of disease activity, but CXCL13 also had utility as a treatment biomarker.
Предметные рубрики MeSH
AdolescentAdrenal Cortex HormonesAdrenocorticotropic HormoneAnalysis of VarianceAntigens, CDB-LymphocytesCase-Control StudiesCell MovementChemokine CXCL12Chemokine CXCL13ChildChild, PreschoolCross-Sectional StudiesEnzyme-Linked Immunosorbent AssayFemaleFlow CytometryHumansImmunoglobulins, IntravenousInfantLongitudinal StudiesMaleOpsoclonus-Myoclonus SyndromeReceptors, CXCR5