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Kiryluk, K., Moldoveanu, Z., Sanders, J.T., Eison, T.M., Suzuki, H., Julian, B.A., et al. (2011) Aberrant Glycosylation of IgA1 Is Inherited in Both Pediatric IgA Nephropathy and Henoch-Schönlein Purpura Nephritis. Kidney International, 80, 79-87.
https://doi.org/10.1038/ki.2011.16

has been cited by the following article:

• TITLE: Three-Month-Induction Therapy with Prednisone and Mycophenolate Followed by Maintenance Therapy with Mycophenolate Alone for 2 Years: An Effective and Safe Autoimmune Treatment for Triggering Factors Adults with Acute Non-Crescentic Nephritis Associated with Henoch-Schönlein Purpura

  AUTHORS: Kamel El-Reshaid, Shaikha Al-Bader, John Madda

  KEYWORDS: Acute, Henoch-Schönlein Purpura, Treatment, Nephrotic Syndrome, Nephritis, Mycophenolate Mofetil

  JOURNAL NAME: Open Journal of Nephrology, Vol.12 No.1, March 23, 2022

  ABSTRACT: Background: Henoch-Schönlein purpura (HSP) is an acute systemic disorder characterized by IgA associated vasculitis. The available data indicate an inherited predisposition to disease with triggering autoimmune phenomena. Hence, we evaluated prospectively the role of a new autoimmune regimen in treatment of its severe nephrotic/nephritic flares associated with non-crescentic nephritis in adult patients. Patients and methods: The regimen consisted of an initial induction phase of 3-month Prednisone and Mycophenolate followed by a maintenance phase of Mycophenolate alone for 2 years. Results: They were satisfactory with complete remission in 5 of 7 patients and partial in 2. Creatinine clearance was normalized in patients with complete remission and remained stable in the partially-responsive ones. Conclusion: Our study has shown the short- and long-term safety and efficacy of such autoimmune regimen directed towards the autoimmune triggering factors in severe forms of non-crescentic HSP.