Heterogeneity in myasthenia gravis: considerations for disease management. (3rd July 2021)
- Record Type:
- Journal Article
- Title:
- Heterogeneity in myasthenia gravis: considerations for disease management. (3rd July 2021)
- Main Title:
- Heterogeneity in myasthenia gravis: considerations for disease management
- Authors:
- Evoli, Amelia
Spagni, Gregorio
Monte, Gabriele
Damato, Valentina - Abstract:
- ABSTRACT: Introduction : Myasthenia gravis is a rare disease of the neuromuscular junction and a prototype of B cell-driven immunopathology. Pathogenic antibodies target post-synaptic transmembrane proteins, most commonly the nicotinic acetylcholine receptor and the muscle-specific tyrosine kinase, inducing end-plate alterations and neuromuscular transmission impairment. Several clinical subtypes are distinct on the basis of associated antibodies, age at symptom onset, thymus pathology, genetic factors, and weakness distribution. These subtypes have distinct pathogenesis that can account for different responses to treatment. Conventional therapy is based on the use of symptomatic agents, steroids, immunosuppressants and thymectomy. Of late, biologics have emerged as effective therapeutic options. Areas covered : In this review, we will discuss the management of myasthenia gravis in relation to its phenotypic and biological heterogeneity, in the light of recent advances in the disease immunopathology, new diagnostic tools, and results of clinical trials Expert opinion : Clinical management is shaped on serological subtype, and patient age at onset, lifestyle and comorbidities, balancing therapeutic needs and safety. Although reliable biomarkers predictive of clinical and biologic outcome are still lacking, recent developments promise a more effective and safe treatment. Disease subtyping according to serological testing and immunopathology is crucial to the appropriateness ofABSTRACT: Introduction : Myasthenia gravis is a rare disease of the neuromuscular junction and a prototype of B cell-driven immunopathology. Pathogenic antibodies target post-synaptic transmembrane proteins, most commonly the nicotinic acetylcholine receptor and the muscle-specific tyrosine kinase, inducing end-plate alterations and neuromuscular transmission impairment. Several clinical subtypes are distinct on the basis of associated antibodies, age at symptom onset, thymus pathology, genetic factors, and weakness distribution. These subtypes have distinct pathogenesis that can account for different responses to treatment. Conventional therapy is based on the use of symptomatic agents, steroids, immunosuppressants and thymectomy. Of late, biologics have emerged as effective therapeutic options. Areas covered : In this review, we will discuss the management of myasthenia gravis in relation to its phenotypic and biological heterogeneity, in the light of recent advances in the disease immunopathology, new diagnostic tools, and results of clinical trials Expert opinion : Clinical management is shaped on serological subtype, and patient age at onset, lifestyle and comorbidities, balancing therapeutic needs and safety. Although reliable biomarkers predictive of clinical and biologic outcome are still lacking, recent developments promise a more effective and safe treatment. Disease subtyping according to serological testing and immunopathology is crucial to the appropriateness of clinical management. … (more)
- Is Part Of:
- Expert review of clinical immunology. Volume 17:Number 7(2021)
- Journal:
- Expert review of clinical immunology
- Issue:
- Volume 17:Number 7(2021)
- Issue Display:
- Volume 17, Issue 7 (2021)
- Year:
- 2021
- Volume:
- 17
- Issue:
- 7
- Issue Sort Value:
- 2021-0017-0007-0000
- Page Start:
- 761
- Page End:
- 771
- Publication Date:
- 2021-07-03
- Subjects:
- Myasthenia gravis -- acetylcholine receptor -- muscle-specific tyrosine kinase -- autoantibodies -- immunotherapy -- rituximab
Clinical immunology -- Periodicals
616.079 - Journal URLs:
- http://www.tandfonline.com/toc/ierm20/current ↗
http://www.future-drugs.com/loi/eci ↗
http://informahealthcare.com ↗ - DOI:
- 10.1080/1744666X.2021.1936500 ↗
- Languages:
- English
- ISSNs:
- 1744-666X
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3842.002985
British Library DSC - BLDSS-3PM
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British Library HMNTS - ELD Digital store - Ingest File:
- 18810.xml