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...
- Autores:
- 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
- Rights
- License
- Restringido (Acceso a grupos específicos)
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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 |
_version_ |
1814167463067123712 |