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Use of rituximab in muscle-specific tyrosine kinase antibody-positive myasthenia gravis: Preliminary observations from a tertiary care center in Northern India
OBJECTIVES: Approximately 10%–15% of patients with myasthenia gravis (MG) are refractory to standard treatment. A sizable chunk of these patients is due to muscle-specific tyrosine kinase (MuSK) antibody-positive MG which often runs a severe course with frequent relapses and poor response to convent...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer - Medknow
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7074426/ https://www.ncbi.nlm.nih.gov/pubmed/32201447 http://dx.doi.org/10.4103/ijp.IJP_333_18 |
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author | Sachdeva, Julie Mahesh, Karthik Vinay Shree, Ritu Jain, Gaurav Kapila, Aastha Takkar Shashikala, Tirulapati Padmavathi Goyal, Manoj Kumar Modi, Manish Lal, Vivek |
author_facet | Sachdeva, Julie Mahesh, Karthik Vinay Shree, Ritu Jain, Gaurav Kapila, Aastha Takkar Shashikala, Tirulapati Padmavathi Goyal, Manoj Kumar Modi, Manish Lal, Vivek |
author_sort | Sachdeva, Julie |
collection | PubMed |
description | OBJECTIVES: Approximately 10%–15% of patients with myasthenia gravis (MG) are refractory to standard treatment. A sizable chunk of these patients is due to muscle-specific tyrosine kinase (MuSK) antibody-positive MG which often runs a severe course with frequent relapses and poor response to conventional treatment. We report six patients with refractory MuSK-positive MG who responded well to the treatment with rituximab. PATIENTS AND METHODS: In this prospective institute-based observational study, we report six MuSK antibody-positive MG patients, who did not achieve remission with standard treatment and were later started on rituximab infusion. RESULTS: There was a significant clinical improvement in all patients after starting rituximab. CONCLUSION: Rituximab is an effective immunomodulatory therapy in MuSK antibody-positive MG patients who are not responding to the standard treatment. |
format | Online Article Text |
id | pubmed-7074426 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Wolters Kluwer - Medknow |
record_format | MEDLINE/PubMed |
spelling | pubmed-70744262020-03-20 Use of rituximab in muscle-specific tyrosine kinase antibody-positive myasthenia gravis: Preliminary observations from a tertiary care center in Northern India Sachdeva, Julie Mahesh, Karthik Vinay Shree, Ritu Jain, Gaurav Kapila, Aastha Takkar Shashikala, Tirulapati Padmavathi Goyal, Manoj Kumar Modi, Manish Lal, Vivek Indian J Pharmacol Short Communication OBJECTIVES: Approximately 10%–15% of patients with myasthenia gravis (MG) are refractory to standard treatment. A sizable chunk of these patients is due to muscle-specific tyrosine kinase (MuSK) antibody-positive MG which often runs a severe course with frequent relapses and poor response to conventional treatment. We report six patients with refractory MuSK-positive MG who responded well to the treatment with rituximab. PATIENTS AND METHODS: In this prospective institute-based observational study, we report six MuSK antibody-positive MG patients, who did not achieve remission with standard treatment and were later started on rituximab infusion. RESULTS: There was a significant clinical improvement in all patients after starting rituximab. CONCLUSION: Rituximab is an effective immunomodulatory therapy in MuSK antibody-positive MG patients who are not responding to the standard treatment. Wolters Kluwer - Medknow 2020 2020-03-11 /pmc/articles/PMC7074426/ /pubmed/32201447 http://dx.doi.org/10.4103/ijp.IJP_333_18 Text en Copyright: © 2020 Indian Journal of Pharmacology http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms. |
spellingShingle | Short Communication Sachdeva, Julie Mahesh, Karthik Vinay Shree, Ritu Jain, Gaurav Kapila, Aastha Takkar Shashikala, Tirulapati Padmavathi Goyal, Manoj Kumar Modi, Manish Lal, Vivek Use of rituximab in muscle-specific tyrosine kinase antibody-positive myasthenia gravis: Preliminary observations from a tertiary care center in Northern India |
title | Use of rituximab in muscle-specific tyrosine kinase antibody-positive myasthenia gravis: Preliminary observations from a tertiary care center in Northern India |
title_full | Use of rituximab in muscle-specific tyrosine kinase antibody-positive myasthenia gravis: Preliminary observations from a tertiary care center in Northern India |
title_fullStr | Use of rituximab in muscle-specific tyrosine kinase antibody-positive myasthenia gravis: Preliminary observations from a tertiary care center in Northern India |
title_full_unstemmed | Use of rituximab in muscle-specific tyrosine kinase antibody-positive myasthenia gravis: Preliminary observations from a tertiary care center in Northern India |
title_short | Use of rituximab in muscle-specific tyrosine kinase antibody-positive myasthenia gravis: Preliminary observations from a tertiary care center in Northern India |
title_sort | use of rituximab in muscle-specific tyrosine kinase antibody-positive myasthenia gravis: preliminary observations from a tertiary care center in northern india |
topic | Short Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7074426/ https://www.ncbi.nlm.nih.gov/pubmed/32201447 http://dx.doi.org/10.4103/ijp.IJP_333_18 |
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