» Articles » PMID: 25308632

Efficacy and Safety of Rituximab for Myasthenia Gravis: a Systematic Review and Meta-analysis

Overview
Journal J Neurol
Specialty Neurology
Date 2014 Oct 14
PMID 25308632
Citations 64
Authors
Affiliations
Soon will be listed here.
Abstract

Myasthenia gravis is an autoimmune disorder of the neuromuscular junction caused by circulating antibodies specific for the post-synaptic acetylcholine receptor or, in a minority of cases, for the muscle-specific tyrosine-kinase and the low-density lipoprotein receptor-related protein 4. A wide range of symptomatic and immunosuppressive treatments is currently available for MG patients with variable outcome. However, most immunosuppressive treatments are characterized by delayed onset of action and in some cases are not sufficient to induce stable remission of the disease. Rituximab (RTX) is a chimaeric monoclonal antibody specific for the CD20 B-cell surface antigen. Recent studies have provided evidence that RTX may be an effective treatment for patients with myasthenia gravis (MG) who are refractory to standardized immunosuppressive therapy. We performed a systematic review and a meta-analysis of the efficacy and safety of RTX in myasthenia gravis considering the potential predictive factors related to patients' response to RTX in this disease.

Citing Articles

Efficacy and safety of different dosages of rituximab for myasthenia gravis: a single-arm meta-analysis.

Li J, Chen D, Zhao F, Cao W, Jin P Daru. 2025; 33(1):15.

PMID: 40085401 DOI: 10.1007/s40199-025-00557-y.


Composition and function of AChR chimeric autoantibody receptor T cells for antigen-specific B cell depletion in myasthenia gravis.

Oh S, Khani-Habibabadi F, OConnor K, Payne A Sci Adv. 2025; 11(9):eadt0795.

PMID: 40020066 PMC: 11870065. DOI: 10.1126/sciadv.adt0795.


Eculizumab in thymoma-associated myasthenia gravis: a real-world cohort study.

Jin L, He D, Zeng Q, Tan S, Shi J, Liu Y Ther Adv Neurol Disord. 2024; 17:17562864241309431.

PMID: 39735403 PMC: 11672488. DOI: 10.1177/17562864241309431.


Retrospective Analysis of Rituximab Therapy for Myasthenia Gravis: A Case Series.

Albalawi A, Alharbi M, Albalawi T Cureus. 2024; 16(11):e74372.

PMID: 39588530 PMC: 11586585. DOI: 10.7759/cureus.74372.


Efficacy and safety of low-dose rituximab in the treatment of myasthenia gravis: a systemic review and meta-analysis.

Yang X, Zhang W, Guo J, Ma C, Li B Front Neurol. 2024; 15:1439899.

PMID: 39385818 PMC: 11461331. DOI: 10.3389/fneur.2024.1439899.


References
1.
Stieglbauer K, Topakian R, Schaffer V, Aichner F . Rituximab for myasthenia gravis: three case reports and review of the literature. J Neurol Sci. 2009; 280(1-2):120-2. DOI: 10.1016/j.jns.2009.02.357. View

2.
Kuntzer T, Carota A, Novy J, Cavassini M, Du Pasquier R . Rituximab is successful in an HIV-positive patient with MuSK myasthenia gravis. Neurology. 2011; 76(8):757-8. DOI: 10.1212/WNL.0b013e31820d6290. View

3.
Sun F, Ladha S, Yang L, Liu Q, Shi S, Su N . Interleukin-10 producing-B cells and their association with responsiveness to rituximab in myasthenia gravis. Muscle Nerve. 2013; 49(4):487-94. DOI: 10.1002/mus.23951. View

4.
Yi J, Decroos E, Sanders D, Weinhold K, Guptill J . Prolonged B-cell depletion in MuSK myasthenia gravis following rituximab treatment. Muscle Nerve. 2013; 48(6):992-3. PMC: 4230922. DOI: 10.1002/mus.24063. View

5.
Lau A, Chan A, Mok V . Refractory bulbar and respiratory dysfunction in a young Chinese woman with seronegative, muscle-specific tyrosine kinase antibody-positive myasthenia gravis: response to cyclophosphamide and rituximab treatment. Hong Kong Med J. 2011; 17(1):77-9. View