• J. Am. Soc. Nephrol. · Aug 2011

    Rituximab-induced depletion of anti-PLA2R autoantibodies predicts response in membranous nephropathy.

    • Laurence H Beck, Fernando C Fervenza, David M Beck, Ramon G B Bonegio, Fahim A Malik, Stephen B Erickson, Fernando G Cosio, Daniel C Cattran, and David J Salant.
    • Department of Medicine, Section of Nephrology, Boston University School of Medicine, Boston, Massachusetts, USA. lhbeckjr@bu.edu
    • J. Am. Soc. Nephrol. 2011 Aug 1; 22 (8): 1543-50.

    AbstractAutoantibodies to the M-type phospholipase A(2) receptor (PLA(2)R) are sensitive and specific for idiopathic membranous nephropathy. The anti-B cell agent rituximab is a promising therapy for this disease, but biomarkers of early response to treatment currently do not exist. Here, we investigated whether levels of anti-PLA(2)R correlate with the immunological activity of membranous nephropathy, potentially exhibiting a more rapid response to treatment than clinical parameters such as proteinuria. We measured the amount of anti-PLA(2)R using Western blot immunoassay in serial serum samples from a total of 35 patients treated with rituximab for membranous nephropathy in two distinct cohorts. Pretreatment samples from 25 of 35 (71%) patients contained anti-PLA(2)R, and these autoantibodies declined or disappeared in 17 (68%) of these patients within 12 months after rituximab. Those who demonstrated this immunologic response fared better clinically: 59% and 88% attained complete or partial remission by 12 and 24 months, respectively, compared with 0% and 33% among those with persistent anti-PLA(2)R levels. Changes in antibody levels preceded changes in proteinuria. One subject who relapsed during follow-up had a concomitant return of anti-PLA(2)R. In summary, measuring anti-PLA(2)R levels by immunoassay may be a method to follow and predict response to treatment with rituximab in membranous nephropathy.

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