Multiple sclerosis is a chronic inflammatory and demyelinating disease of t
he CNS with, as yet, an unknown aetiology. Temporal profile, intensity and
treatment responses are highly variable in multiple sclerosis suggesting pa
thogenetic heterogeneity. This hypothesis has been supported by histopathol
ogical studies disclosing at least four different subtypes of acute demyeli
nating lesions. Although stratification of multiple sclerosis patients into
these categories would be extremely helpful for clinical studies, this app
roach is impractical as it requires brain biopsy. In this study we investig
ated CSF cytology from 60 multiple sclerosis patients by flow cytometry. We
identified different patterns of CSF cytology, which were independent of i
mmunological parameters in the peripheral blood. The most variable CSF para
meter was the B cell to monocyte ratio, which remained stable during differ
ent phases of disease in selected patients. The ratio correlated with disea
se progression but not with disability or disease duration in a retrospecti
ve, consecutive analysis. A high ratio (predominance of B cells) was associ
ated with more rapid disease progression, whereas a low ratio (predominance
of monocytes) was found in patients with slower progression. Our study dem
onstrates the existence and potential clinical relevance of different CSF c
ytology patterns. We hypothesize that CSF cytology patterns may reflect the
heterogeneity in the pathogenesis of multiple sclerosis.