P. Lamprecht et al., Immunological and clinical follow up of hepatitis C virus associated cryoglobulinaemic vasculitis, ANN RHEUM D, 60(4), 2001, pp. 385-390
Objective-To study immunological markers and compare these markers with sta
ndard measures for the clinical and immunological follow up of vasculitis a
ctivity in hepatitis C virus (HCV) associated cryoglobulinaemic vasculitis
(CV).
Methods-Serial serum samples from eight patients with newly diagnosed HCV a
ssociated CV were followed during interferon a treatment induced remission
of the CV. Vasculitis activity and disease extent were evaluated with the B
irmingham vasculitis activity score (BVAS) and disease extent index (DEI).
Cryoglobulinaemia, complement levels (C3c, C4, and CH50), rheumatoid factor
(RF), autoantibodies such as antinuclear antibodies, soluble interleukin 2
receptor (sIL2r), soluble intercellular adhesion molecule-1 (sICAM-1), and
soluble CD30 (sCD30) were determined.
Results-All patients achieved either complete or partial remission of their
CV during interferon a treatment. There was a significant reduction in vas
culitis activity and disease extent (BVAS, DEI), cryoglobulinaemia, RF, sIL
2r, sICAM-1, and sCD30. Complement C3c levels increased significantly durin
g this period. Erythrocyte sedimentation rate and levels of complement C4 a
nd CH50 did not change significantly. Both clinical measures (BVAS and DEI)
correlated significantly only with C3c and sCD30.
Conclusions-Although this study was of only a small group of patients, it s
hows that BVAS and DEI as clinical measures and C3c and sCD30 as immunologi
cal markers may be useful in the follow up of disease activity of HCV assoc
iated CV. The data indicate that activity of the humoral (cryoglobulinaemia
, RF, autoantibodies) and cellular (sIL2r, sICAM-1, sCD30) immune response
and endothelial damage (sICAM-1) are found in HCV associated CV.