Adverse Prognosis in Membranous Nephropathy with PLA2R1 Epitope Spreading: A Prospective Study.

Abstract

Background: In primary membranous nephropathy (MN), 80% of patients harbor antibodies against phospholipase A2 receptor 1 (PLA2R1), closely linked to disease prognosis. Prior research has validated the correlation between antibodies directed towards the cysteine-rich(CysR) and C-type lectin 1, 7, and 8(CTLD1, CTLD7, and CTLD8) domains of PLA2R1 and outcomes in MN.

Methods: In a prospective cohort of 52 patients with newly diagnosed PLA2R1-MN, with urine protein ≥ 3.5 g/24 hours and estimated glomerular filtration rate ≥30 mL/min/1.73 m², we studied epitope-spreading patterns and domain-specific PLA2R1-Ab clinically using western blot and ELISA. The primary outcome was a combination of remission at 12 months. Kaplan-Meier curves and Multivariable Cox regression were employed to compare the single and multiple epitope patients.

Results: All patients had anti-CysR antibodies. 26(50.0%) exhibited multi-domain recognition, with one patient specifically recognizing the CTLD8 domain. A significant association was observed between PLA2R1-Ab and CysR-Ab(r = 0.869, P ＜0.001), as well as with anti-CTLD1 antibody(r = 0.803, P ＜0.001). During a median follow-up of 11 months(IQR, 6.0-17.0), 27 patients(65.9%) experienced complete or partial nephrotic syndrome remission. Notably, the multi-domain recognition exhibited a reduced remission rate compared to the single-domain(44.44% vs 82.61%, P = 0.011, alongside higher concentrations of anti-PLA2R1 antibodies. A higher baseline level of anti-CTLD1 was notably linked to a lower likelihood of remission. In a univariate analysis, multi-domain recognition decreases the probability of remission[HR, 0.38 (95% CI, 0.16-0.87), P = 0.022]. After the Kaplan-Meier analysis, the multi-domain group showed lower remission rates than the single-domain group at various time points.

Conclusion: The PLA2R1 epitope spreading is a potent tool for monitoring disease severity and stratifying patients based on renal outcomes for prognostic purposes. Hence, we advocate evaluating epitope spreading at the baseline stage when determining early therapeutic interventions for individuals diagnosed with MN.