Favorable long-term outcomes of autoimmune nodopathy with mycophenolate mofetil

Autoimmune nodopathy (AN) is a rare immune-mediated neuropathy characterized by autoantibodies against nodal or paranodal proteins. Patients with AN generally respond poorly to immunoglobulin therapy, and as a newly defined condition, there are currently no established treatment guidelines. Although rituximab shows potential as a therapeutic option, its high cost, limited availability, and the need for infusion monitoring hinder its use as a first-line treatment in many countries. In this report, we identified AN antibodies in five of 106 serum samples (4.7%) prospectively collected from patients initially diagnosed with chronic inflammatory demyelinating polyradiculoneuropathy (CIDP): anti-neurofascin 155 (NF155) in 2 patients, anti-contactin-1 (CNTN1) in 1, anti-contactin associated protein 1 (CASPR1), and anti-NF186/140 in 1. Notably, we observed favorable long-term outcomes in these patients following treatment with mycophenolate mofetil (MMF) and corticosteroids. Given that these patients had not responded to immunoglobulin therapy and/or experienced relapses with corticosteroid monotherapy in their prior episodes, we propose MMF as a cost-effective treatment strategy for AN.

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Publication Details

Journal
Frontiers in Neurology
Published
2024-12-12
DOI
https://doi.org/10.3389/fneur.2024.1515161
Citations
1
Primary Topic
Peripheral Neuropathies and Disorders
Type
article
Field-Weighted Citation Impact
0.37

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article

Favorable long-term outcomes of autoimmune nodopathy with mycophenolate mofetil

Jung‐Joon Sung, Young Gi Min, Woohee Ju
1 citations
Frontiers in Neurology
Peripheral Neuropathies and Disorders
0.37
article

Favorable long-term outcomes of autoimmune nodopathy with mycophenolate mofetil

Jung‐Joon Sung, Young Gi Min, Woohee Ju
article en
1 citations

Abstract

Autoimmune nodopathy (AN) is a rare immune-mediated neuropathy characterized by autoantibodies against nodal or paranodal proteins. Patients with AN generally respond poorly to immunoglobulin therapy, and as a newly defined condition, there are currently no established treatment guidelines. Although rituximab shows potential as a therapeutic option, its high cost, limited availability, and the need for infusion monitoring hinder its use as a first-line treatment in many countries. In this report, we identified AN antibodies in five of 106 serum samples (4.7%) prospectively collected from patients initially diagnosed with chronic inflammatory demyelinating polyradiculoneuropathy (CIDP): anti-neurofascin 155 (NF155) in 2 patients, anti-contactin-1 (CNTN1) in 1, anti-contactin associated protein 1 (CASPR1), and anti-NF186/140 in 1. Notably, we observed favorable long-term outcomes in these patients following treatment with mycophenolate mofetil (MMF) and corticosteroids. Given that these patients had not responded to immunoglobulin therapy and/or experienced relapses with corticosteroid monotherapy in their prior episodes, we propose MMF as a cost-effective treatment strategy for AN.

Frontiers in NeurologyVol. 15
Seoul National University (KR), Seoul National University Hospital (KR), Chung-Ang University Hospital (KR)
National Research Foundation, Seoul National University, National Research Foundation of Korea, Seoul National University Hospital
Openalex Percentile: Top 32%
Peripheral Neuropathies and Disorders
0.37
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