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Published on: December 1, 2023
New autoimmune disorder development after immune reconstitution therapy for multiple sclerosis
Nataša Giedraitienė1, Rasa Kizlaitienė2, Gintaras Kaubrys2
1Clinic of Neurology and Neurosurgery, Institute of Clinical Medicine, Faculty of Medicine, Vilnius University, Vilnius, Lithuania. natasa.giedraitiene@gmail.com.
Immune reconstitution therapies (IRT) can lead to new autoimmune disorders (ADs) in multiple sclerosis (MS) patients. Alemtuzumab and autologous hematopoietic stem cell transplantation show higher risks of ADs compared to cladribine.
Area of Science:
- Neurology
- Immunology
- Clinical Medicine
Background:
- Immune reconstitution therapy (IRT) offers a highly effective treatment for multiple sclerosis (MS).
- The potential for developing secondary autoimmune disorders (ADs) after certain IRTs requires further investigation.
- Understanding the incidence and characteristics of post-IRT ADs is crucial for patient management.
Purpose of the Study:
- To evaluate the incidence of new AD development in MS patients following IRT.
- To characterize the types of ADs that emerge after IRT.
- To determine the time to onset for these secondary ADs.
Main Methods:
- Retrospective analysis of 179 relapsing MS patients treated with IRT over ten years.
- Categorization of IRT into autologous hematopoietic stem cell transplantation (AHSCT), alemtuzumab (ALE), and cladribine (CLA).
- Monitoring and documentation of new AD development and time to onset post-treatment.
Main Results:
- Overall AD incidence varied by IRT: 16.2% after AHSCT, 42.1% after ALE, and 1.6% after CLA.
- ADs emerged sooner after alemtuzumab but later after AHSCT (excluding cytopenias).
- Alemtuzumab and AHSCT were associated with a higher risk of secondary ADs in MS patients.
Conclusions:
- Neurologists must remain vigilant for secondary AD development in MS patients treated with alemtuzumab and AHSCT.
- The risk and timing of ADs differ significantly among various IRT modalities.
- Further research into the mechanisms and management of post-IRT ADs is warranted.
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