Jbg. Bell et al., NEUTRALIZING ANTIBODIES IN PATIENTS WITH MULTIPLE-MYELOMA RECEIVING MAINTENANCE THERAPY WITH INTERFERON ALPHA(2B), British Journal of Cancer, 70(4), 1994, pp. 646-651
In a study of 29 patients who were receiving or had received interfero
n alpha(2b) (IFN-alpha(2b)) as maintenance therapy for multiple myelom
a, antibodies were detected in 58% (17/29) of patients measured by a s
olid-phase enzyme-linked immunosorbent assay (ELISA). Only 7/17 patien
ts who were positive for antibody in the ELISA had neutralising antibo
dy to IFN-alpha(2b), measured by virus growth inhibition. These patien
ts comprised six who were receiving IFN-alpha(2b) at the time of asses
sment and one who had finished treatment. Among patients who were rece
iving the cytokine, four had progressive disease, one was in complete
remission and one in partial remission. Neutralising activity was also
detected to natural human leucocyte IFN-alpha in the same patients. T
wo patients who were positive for neutralising antibody remain in remi
ssion and are continuing to receive IFN-alpha(2b). These two patients
have since lost their neutralising titre. No neutralising antibody to
IFN-alpha(2b) or natural human leucocyte IFN-alpha was detected in ser
um from six normal donors. The data suggest that neutralising antibody
formation in patients with multiple myeloma is not responsible for re
lapse in patients receiving IFN-alpha(2b). The transient nature of neu
tralising antibody production in patients who remain in remission sugg
ests that this response to IFN-alpha(2b) is not associated with memory
B cells.