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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...

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Autores principales: Sachdeva, Julie, Mahesh, Karthik Vinay, Shree, Ritu, Jain, Gaurav, Kapila, Aastha Takkar, Shashikala, Tirulapati Padmavathi, Goyal, Manoj Kumar, Modi, Manish, Lal, Vivek
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2020
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.
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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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