K. Gross et al., INDUCTION OF DOUBLE-STRANDED DNA ANTIBODI ES BY SULFASALAZINE TREATMENT - A PHENOMENON WITHOUT CLINICAL-SIGNIFICANCE, Aktuelle Rheumatologie, 21(1), 1996, pp. 33-36
The induction of a lupus-like syndrome by treatment with sulphasalzine
(SAS) is so far only reported in single cases. After observing this p
henomenon in a few cases we investigated prospectively the value, inci
dence and in some cases the long-term outcome of 103 patients receivin
g SAS-treatment. 18 patients (17 %) developed new ds-DNS-antibodies. 1
7 (of 77) patients had SAS because of rheumatoid arthritis, only one p
atient (of 26) suffered from a HLA-B27 associated spondarthropathy. Tw
o of the patients developed a lupus-like syndrome (fever leukopenia, e
rythema), which dissolved after discontinuing the treatment. The 18 pa
tients who developed ds-DNA-antibodies could be followed for a longer
period. In twelve cases SAS treatment was stopped because of the high
antibody titre or because of insufficiency. In all these cases there w
ere no more ds-DNA antibodies detectable after six months. Six of the
patients received further treatment with SAS despite their development
of antibodies without clinical consequences. Our results show a frequ
ent development of ds-DNA antibodies by SAS treatment especially in pa
tients with rheumatoid arthritis, only single cases in patients with H
LA-B27 associated spondarthropathy. A lupus-like syndrome in neverthel
ess very rare. Our experiences show that SAS-treatment doesn't have to
be discontinued as soon as antibodies develop, but there has to be a
close follow-up of these patients.