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Treatment of early arthritis using arthrofoon (ultra-low doses of antibodies to tumor necrosis factor-α)

The main aim of treatment of early rheumatoid arthritis (RA) should be to achieve clinical remission to prevent structural damage and physical disability. Arthrofoon modifies production/activity of endogenous inhibitors of tumor necrosis factor-α (TNF-α). The sublingual rout is the most acceptable t...

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Autor principal: Sizova, Lyudmila V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3229795/
https://www.ncbi.nlm.nih.gov/pubmed/22144784
http://dx.doi.org/10.4103/0253-7613.89836
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author Sizova, Lyudmila V.
author_facet Sizova, Lyudmila V.
author_sort Sizova, Lyudmila V.
collection PubMed
description The main aim of treatment of early rheumatoid arthritis (RA) should be to achieve clinical remission to prevent structural damage and physical disability. Arthrofoon modifies production/activity of endogenous inhibitors of tumor necrosis factor-α (TNF-α). The sublingual rout is the most acceptable to ambulatory treatment because it does not produce the adverse reactions associated with intravenous therapy. The treatment with arthrofoon in outpatient with early RA is analyzed here. This report is devoted to the 28-year-old Russian woman who received arthrofoon due to suspicion of early RA. The strategy of early prescription of ultra-low doses of TNF-α antibody within two years was confirmed by the clinical improvement and delay of radiological disease progression in patient with undifferentiated arthritis or probable RA initially.
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spelling pubmed-32297952011-12-05 Treatment of early arthritis using arthrofoon (ultra-low doses of antibodies to tumor necrosis factor-α) Sizova, Lyudmila V. Indian J Pharmacol Drug Watch The main aim of treatment of early rheumatoid arthritis (RA) should be to achieve clinical remission to prevent structural damage and physical disability. Arthrofoon modifies production/activity of endogenous inhibitors of tumor necrosis factor-α (TNF-α). The sublingual rout is the most acceptable to ambulatory treatment because it does not produce the adverse reactions associated with intravenous therapy. The treatment with arthrofoon in outpatient with early RA is analyzed here. This report is devoted to the 28-year-old Russian woman who received arthrofoon due to suspicion of early RA. The strategy of early prescription of ultra-low doses of TNF-α antibody within two years was confirmed by the clinical improvement and delay of radiological disease progression in patient with undifferentiated arthritis or probable RA initially. Medknow Publications & Media Pvt Ltd 2011 /pmc/articles/PMC3229795/ /pubmed/22144784 http://dx.doi.org/10.4103/0253-7613.89836 Text en Copyright: © Indian Journal of Pharmacology http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Drug Watch
Sizova, Lyudmila V.
Treatment of early arthritis using arthrofoon (ultra-low doses of antibodies to tumor necrosis factor-α)
title Treatment of early arthritis using arthrofoon (ultra-low doses of antibodies to tumor necrosis factor-α)
title_full Treatment of early arthritis using arthrofoon (ultra-low doses of antibodies to tumor necrosis factor-α)
title_fullStr Treatment of early arthritis using arthrofoon (ultra-low doses of antibodies to tumor necrosis factor-α)
title_full_unstemmed Treatment of early arthritis using arthrofoon (ultra-low doses of antibodies to tumor necrosis factor-α)
title_short Treatment of early arthritis using arthrofoon (ultra-low doses of antibodies to tumor necrosis factor-α)
title_sort treatment of early arthritis using arthrofoon (ultra-low doses of antibodies to tumor necrosis factor-α)
topic Drug Watch
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3229795/
https://www.ncbi.nlm.nih.gov/pubmed/22144784
http://dx.doi.org/10.4103/0253-7613.89836
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