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. 2024 Dec 28;14(1):30991.
doi: 10.1038/s41598-024-82196-y.

New autoimmune disorder development after immune reconstitution therapy for multiple sclerosis

Affiliations

New autoimmune disorder development after immune reconstitution therapy for multiple sclerosis

Nataša Giedraitienė et al. Sci Rep. .

Abstract

Immune reconstitution therapy (IRT) is a relatively new and highly effective treatment option for multiple sclerosis (MS). Uncertainty regarding the development of autoimmune disorders (ADs) after some therapies remains. The aim of this study was to assess new AD development after IRT in MS patients and to describe the nature of those ADs and the time to onset. A total of 179 patients with relapsing multiple sclerosis (37 after autologous haematopoietic stem cell transplantation (AHSCT), 19 after alemtuzumab (ALE) and 123 after cladribine (CLA) treatment) over a ten year period were included in the study. ADs were observed in 6 patients (16.2%) after AHSCT, 8 patients (42.1%) after ALE and 2 patients (1.6%) after CLA treatment. ADs developed earlier after ALE infusions, but later after AHSCT except for cytopenias. Neurologists should be attentive to the development of secondary ADs after ALE and AHSCT in MS patients.

Keywords: Alemtuzumab; Autoimmune disorder; Autologous haematopoietic stem cell transplantation; Cladribine; Immune reconstitution therapy; Relapsing multiple sclerosis.

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Conflict of interest statement

Declarations. Competing interests: The authors declare no competing interests.

Figures

Fig. 1
Fig. 1
Occurrence of secondary AD per year of follow-up in MS patients treated with AHSCT. 1,—up to 12 months; 2,—13 −24 months; 3,—25–36 months; 4,—37–48 months; 5,—49–60 months; 6,—> 60 months. AD,—autoimmune disorder; AHSCT,—autologous haematopoietic stem cell transplantation. The number of patients with AD is shown in black relative to the total number of treated patients in grey.
Fig. 2
Fig. 2
Occurrence of secondary AD per year of follow-up in MS patients treated with ALE. 1,—up to 12 months; 2,—13 −24 months; 3,—25–36 months; 4,—37–48 months; 5,—49–60 months; 6,—> 60 months. AD,—autoimmune disorder; ALE,—alemtuzumab. The number of patients with AD is shown in black relative to the total number of treated patients in grey.
Fig. 3
Fig. 3
Occurrence of secondary AD per year of follow-up in MS patients treated with CLA. 1,—up to 12 months; 2,—13–24 months; 3,—25–36 months; 4,—37–48 months; 5,—49–60 months; 6,—> 60 months. AD,—autoimmune disorder; CLA,—cladribine. The number of patients with AD is shown in black relative to the total number of treated patients in grey.

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