R. Schiel et al., CYCLOSPORINE AND THERAPEUTIC PLASMA-EXCHANGE IN TREATMENT OF PROGRESSIVE AUTOIMMUNE-DISEASES, Artificial organs, 21(9), 1997, pp. 983-988
Despite treatment with intensive immunosuppressive drug regimens, the
prognosis of patients suffering from severe progressive autoimmune dis
eases like systemic lupus erythematosus (SLE), nephrotic syndrome (NS)
, and Behcet's disease is poor. Side effects (infections and malignant
tumors) often occur. In the present trial, 35 patients suffering from
autoimmune diseases (SLE, n = 21; NS, n = 10; and Behcet's disease, n
= 4) were treated for 3.7 +/- 2.0 years with 2.5 +/- 0.6 mg cyclospor
ine/kg body weight/day in addition to corticosteroids alone or in comb
ination with azathioprine and/or cyclophosphamide. In active stages of
the diseases with extremely high concentrations of anti-ds-DNA-antibo
dies, antinuclear antibodies, circulating immunocomplexes, and reduced
complement concentrations, therapeutic plasma exchange (TPE) has been
applied. Compared with previous treatment modalities, significantly (
p < 0.05) more effective and rapid reductions of the antibodies were r
eached. Clinical disorders improved within 1-6 weeks. All patients rep
orted increased performance and a better quality of life. After 1-12 m
onths, the previously required doses of immunosuppressive drugs and th
e frequency of TPE could be reduced by 40-100%. After 13.4 +/- 11.8 mo
nths in 17 of 35 patients (8 with SLE, 5 with NS, 4 with Behcet's dise
ase), cyclosporine was established as the monotherapy. No severe side
effects were registered. In treating active stages of severe progressi
ve autoimmune diseases and forms with persistent high antibody levels,
the addition of TPE to conventional therapy was very effective, as ob
served in both clinical and laboratory parameters.