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B Cell Depletion Treatment in Resistant Systemic Sclerosis Interstitial Lung Disease

Systemic sclerosis is a systemic, autoimmune disease that in many patients affects not only the skin, but also internal organs, mainly the lung. It is clear that internal organ (ie, lung) involvement determines the prognosis. Therefore, there is an unmet need to introduce novel and more effective tr...

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Detalles Bibliográficos
Autores principales: Bounia, Constantina A., Liossis, Stamatis-Nick C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Mediterranean Journal of Rheumatology (MJR) 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9092104/
https://www.ncbi.nlm.nih.gov/pubmed/35611107
http://dx.doi.org/10.31138/mjr.33.1.1
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author Bounia, Constantina A.
Liossis, Stamatis-Nick C.
author_facet Bounia, Constantina A.
Liossis, Stamatis-Nick C.
author_sort Bounia, Constantina A.
collection PubMed
description Systemic sclerosis is a systemic, autoimmune disease that in many patients affects not only the skin, but also internal organs, mainly the lung. It is clear that internal organ (ie, lung) involvement determines the prognosis. Therefore, there is an unmet need to introduce novel and more effective treatments capable of halting disease progression and hence improve prognosis. Experimental data over the past decade has accumulated pointing to the B cell as a player in disease pathogenesis. Consequently, a number of controlled and uncontrolled studies have investigated the results of B cell depletion treatment in patients with SSc. The results are preliminary still encouraging for skin as well as for pulmonary involvement. In this review we will analyse and discuss such trials that have currently added B cell depletion as an alternative and promising treatment for resistant interstitial lung disease in scleroderma.
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spelling pubmed-90921042022-05-23 B Cell Depletion Treatment in Resistant Systemic Sclerosis Interstitial Lung Disease Bounia, Constantina A. Liossis, Stamatis-Nick C. Mediterr J Rheumatol Review Systemic sclerosis is a systemic, autoimmune disease that in many patients affects not only the skin, but also internal organs, mainly the lung. It is clear that internal organ (ie, lung) involvement determines the prognosis. Therefore, there is an unmet need to introduce novel and more effective treatments capable of halting disease progression and hence improve prognosis. Experimental data over the past decade has accumulated pointing to the B cell as a player in disease pathogenesis. Consequently, a number of controlled and uncontrolled studies have investigated the results of B cell depletion treatment in patients with SSc. The results are preliminary still encouraging for skin as well as for pulmonary involvement. In this review we will analyse and discuss such trials that have currently added B cell depletion as an alternative and promising treatment for resistant interstitial lung disease in scleroderma. The Mediterranean Journal of Rheumatology (MJR) 2022-03-31 /pmc/articles/PMC9092104/ /pubmed/35611107 http://dx.doi.org/10.31138/mjr.33.1.1 Text en © 2022 The Mediterranean Journal of Rheumatology (MJR) https://creativecommons.org/licenses/by/4.0/This work is licensed under and Creative Commons Attribution-NonCommercial 4.0 International License.
spellingShingle Review
Bounia, Constantina A.
Liossis, Stamatis-Nick C.
B Cell Depletion Treatment in Resistant Systemic Sclerosis Interstitial Lung Disease
title B Cell Depletion Treatment in Resistant Systemic Sclerosis Interstitial Lung Disease
title_full B Cell Depletion Treatment in Resistant Systemic Sclerosis Interstitial Lung Disease
title_fullStr B Cell Depletion Treatment in Resistant Systemic Sclerosis Interstitial Lung Disease
title_full_unstemmed B Cell Depletion Treatment in Resistant Systemic Sclerosis Interstitial Lung Disease
title_short B Cell Depletion Treatment in Resistant Systemic Sclerosis Interstitial Lung Disease
title_sort b cell depletion treatment in resistant systemic sclerosis interstitial lung disease
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9092104/
https://www.ncbi.nlm.nih.gov/pubmed/35611107
http://dx.doi.org/10.31138/mjr.33.1.1
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