Variation in the serum IgA concentration and the production of IgA in vitro in rheumatoid arthritis treated by sulfasalazine

Sulfasalazine is an efficient treatment for rheumatoid arthritis (RA), but its mode of action is not known. In RA, a correlation has been demonstrated between disease activity and the secretion of immunoglobulin A (IgA) by peripheral blood lymphocytes (PBL) in culture. Furthermore, the IgA-producing...

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Tipo de recurso:
Fecha de publicación:
1993
Institución:
Universidad del Rosario
Repositorio:
Repositorio EdocUR - U. Rosario
Idioma:
eng
OAI Identifier:
oai:repository.urosario.edu.co:10336/26008
Acceso en línea:
https://doi.org/10.1007/BF00290298
https://repository.urosario.edu.co/handle/10336/26008
Palabra clave:
Rheumatoid arthritis
Mucous-associated lymphoid tissue
Immunoglobulin A
Sulfasalazine
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id EDOCUR2_7eac15b1f88e482bb2a47bc7ec95bc99
oai_identifier_str oai:repository.urosario.edu.co:10336/26008
network_acronym_str EDOCUR2
network_name_str Repositorio EdocUR - U. Rosario
repository_id_str
spelling 0ffaf063-7823-42e6-9c94-b6fe251a08abe6562e6b-7333-4c58-975d-047badf695a219474778600046b1bf4-71eb-4ffb-a0d7-0bfebd135f05e8938956-af14-46bd-9749-62565a90def12020-08-06T16:20:26Z2020-08-06T16:20:26Z1993-08-01Sulfasalazine is an efficient treatment for rheumatoid arthritis (RA), but its mode of action is not known. In RA, a correlation has been demonstrated between disease activity and the secretion of immunoglobulin A (IgA) by peripheral blood lymphocytes (PBL) in culture. Furthermore, the IgA-producing cells of the peripheral blood have been shown to originate from the mucous-associate lymphoid tissue (MALT). We studied the variations in the total IgA concentration in the serum of RA patients, and the secretion of IgA by PBL after 7 days culture in vitro, before and after treatment with sulfasalazine. A significant decrease in the serum IgA concentraton was obtained, but there was no modification of the spontaneous increase in the in vitro IgA synthesis by circulating monoclear cells. Our results suggested that the decrease in serum IgA concentration after treatment with sulfasalazine was not linked to a decrease in the IgA secretion by PBL. This does not favour a direct effect of sulfasalazine on the mucous-associated lymphoid tissue.application/pdfhttps://doi.org/10.1007/BF00290298ISSN: 0172-8172EISSN: 1437-160Xhttps://repository.urosario.edu.co/handle/10336/26008engSpringer Nature116113Rheumatology InternationalVol. 13Rheumatology International, ISSN: 0172-8172;EISSN: 1437-160X, Vol.13 (August, 1993); pp.113-116https://link.springer.com/article/10.1007/BF00290298Restringido (Acceso a grupos específicos)http://purl.org/coar/access_right/c_16ecRheumatology Internationalinstname:Universidad del Rosarioreponame:Repositorio Institucional EdocURRheumatoid arthritisMucous-associated lymphoid tissueImmunoglobulin ASulfasalazineVariation in the serum IgA concentration and the production of IgA in vitro in rheumatoid arthritis treated by sulfasalazineVariación en la concentración sérica de IgA y la producción de IgA in vitro en artritis reumatoide tratada con sulfasalazinaarticleArtículohttp://purl.org/coar/version/c_970fb48d4fbd8a85http://purl.org/coar/resource_type/c_6501Jorgensen, C.Bologna, C.Anaya, Juan-ManuelReme, T.Sany, J.10336/26008oai:repository.urosario.edu.co:10336/260082021-08-10 21:57:02.594https://repository.urosario.edu.coRepositorio institucional EdocURedocur@urosario.edu.co
dc.title.spa.fl_str_mv Variation in the serum IgA concentration and the production of IgA in vitro in rheumatoid arthritis treated by sulfasalazine
dc.title.TranslatedTitle.eng.fl_str_mv Variación en la concentración sérica de IgA y la producción de IgA in vitro en artritis reumatoide tratada con sulfasalazina
title Variation in the serum IgA concentration and the production of IgA in vitro in rheumatoid arthritis treated by sulfasalazine
spellingShingle Variation in the serum IgA concentration and the production of IgA in vitro in rheumatoid arthritis treated by sulfasalazine
Rheumatoid arthritis
Mucous-associated lymphoid tissue
Immunoglobulin A
Sulfasalazine
title_short Variation in the serum IgA concentration and the production of IgA in vitro in rheumatoid arthritis treated by sulfasalazine
title_full Variation in the serum IgA concentration and the production of IgA in vitro in rheumatoid arthritis treated by sulfasalazine
title_fullStr Variation in the serum IgA concentration and the production of IgA in vitro in rheumatoid arthritis treated by sulfasalazine
title_full_unstemmed Variation in the serum IgA concentration and the production of IgA in vitro in rheumatoid arthritis treated by sulfasalazine
title_sort Variation in the serum IgA concentration and the production of IgA in vitro in rheumatoid arthritis treated by sulfasalazine
dc.subject.keyword.spa.fl_str_mv Rheumatoid arthritis
Mucous-associated lymphoid tissue
Immunoglobulin A
Sulfasalazine
topic Rheumatoid arthritis
Mucous-associated lymphoid tissue
Immunoglobulin A
Sulfasalazine
description Sulfasalazine is an efficient treatment for rheumatoid arthritis (RA), but its mode of action is not known. In RA, a correlation has been demonstrated between disease activity and the secretion of immunoglobulin A (IgA) by peripheral blood lymphocytes (PBL) in culture. Furthermore, the IgA-producing cells of the peripheral blood have been shown to originate from the mucous-associate lymphoid tissue (MALT). We studied the variations in the total IgA concentration in the serum of RA patients, and the secretion of IgA by PBL after 7 days culture in vitro, before and after treatment with sulfasalazine. A significant decrease in the serum IgA concentraton was obtained, but there was no modification of the spontaneous increase in the in vitro IgA synthesis by circulating monoclear cells. Our results suggested that the decrease in serum IgA concentration after treatment with sulfasalazine was not linked to a decrease in the IgA secretion by PBL. This does not favour a direct effect of sulfasalazine on the mucous-associated lymphoid tissue.
publishDate 1993
dc.date.created.spa.fl_str_mv 1993-08-01
dc.date.accessioned.none.fl_str_mv 2020-08-06T16:20:26Z
dc.date.available.none.fl_str_mv 2020-08-06T16:20:26Z
dc.type.eng.fl_str_mv article
dc.type.coarversion.fl_str_mv http://purl.org/coar/version/c_970fb48d4fbd8a85
dc.type.coar.fl_str_mv http://purl.org/coar/resource_type/c_6501
dc.type.spa.spa.fl_str_mv Artículo
dc.identifier.doi.none.fl_str_mv https://doi.org/10.1007/BF00290298
dc.identifier.issn.none.fl_str_mv ISSN: 0172-8172
EISSN: 1437-160X
dc.identifier.uri.none.fl_str_mv https://repository.urosario.edu.co/handle/10336/26008
url https://doi.org/10.1007/BF00290298
https://repository.urosario.edu.co/handle/10336/26008
identifier_str_mv ISSN: 0172-8172
EISSN: 1437-160X
dc.language.iso.spa.fl_str_mv eng
language eng
dc.relation.citationEndPage.none.fl_str_mv 116
dc.relation.citationStartPage.none.fl_str_mv 113
dc.relation.citationTitle.none.fl_str_mv Rheumatology International
dc.relation.citationVolume.none.fl_str_mv Vol. 13
dc.relation.ispartof.spa.fl_str_mv Rheumatology International, ISSN: 0172-8172;EISSN: 1437-160X, Vol.13 (August, 1993); pp.113-116
dc.relation.uri.spa.fl_str_mv https://link.springer.com/article/10.1007/BF00290298
dc.rights.coar.fl_str_mv http://purl.org/coar/access_right/c_16ec
dc.rights.acceso.spa.fl_str_mv Restringido (Acceso a grupos específicos)
rights_invalid_str_mv Restringido (Acceso a grupos específicos)
http://purl.org/coar/access_right/c_16ec
dc.format.mimetype.none.fl_str_mv application/pdf
dc.publisher.spa.fl_str_mv Springer Nature
dc.source.spa.fl_str_mv Rheumatology International
institution Universidad del Rosario
dc.source.instname.none.fl_str_mv instname:Universidad del Rosario
dc.source.reponame.none.fl_str_mv reponame:Repositorio Institucional EdocUR
repository.name.fl_str_mv Repositorio institucional EdocUR
repository.mail.fl_str_mv edocur@urosario.edu.co
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