Natalizumab As a Disease-Modifying Therapy in Chronic Inflammatory Demyelinating Polyneuropathy - A Report of Three Cases
Overview
Authors
Affiliations
Background: Several treatments are available to treat the immune-mediated chronic inflammatory demyelinating polyneuropathy (CIDP). Among these treatments, intravenous immunoglobulins, corticosteroids and plasma exchanges are validated and widely used. A few immunosuppressive drugs have been tried, but they had little efficiency.
Methods: We describe three CIDP patients treated by Natalizumab (acting against cellular adhesion and T-cell migration) after a failure of the validated treatments.
Results: We observed a long-term improvement in one patient, a dramatic improvement over a significant duration in another patient and stabilization in the last one.
Conclusion: This open label study provides evidence for the value of Natalizumab as second-line treatment for individual patients with a high dependency on waning efficacy of first-line therapies. CIDP is characterized by heterogeneity of clinical phenotypes, electrophysiological and pathological features, and various variable courses types of evolution. The different responses to drugs of our patients are consistent with some reported cases and may reflect the spectrum of lesional mechanisms and the molecular dysfunctions in CIDP.
Alawneh I, Alenizi A, Paiz F, Nigro E, Vajsar J, Gonorazky H Paediatr Drugs. 2024; 26(6):709-717.
PMID: 39192168 DOI: 10.1007/s40272-024-00646-6.
Kohle F, Dalakas M, Lehmann H Ther Adv Neurol Disord. 2023; 16:17562864221137129.
PMID: 36620728 PMC: 9810996. DOI: 10.1177/17562864221137129.
Targeting the blood-nerve barrier for the management of immune-mediated peripheral neuropathies.
Stubbs Jr E Exp Neurol. 2020; 331:113385.
PMID: 32562668 PMC: 7484028. DOI: 10.1016/j.expneurol.2020.113385.
Kieseier B, Mathey E, Sommer C, Hartung H Nat Rev Dis Primers. 2018; 4(1):31.
PMID: 30310069 DOI: 10.1038/s41572-018-0027-2.
Mahdi-Rogers M, Brassington R, Gunn A, van Doorn P, Hughes R Cochrane Database Syst Rev. 2017; 5:CD003280.
PMID: 28481421 PMC: 6481566. DOI: 10.1002/14651858.CD003280.pub5.