Loading…

To B or not to B the conductor of Rheumatoid Arthritis orchestra

© Springer Science+Business Media, LLC 2012 Rheumatoid arthritis (RA) is a chronic, systemic immune-mediated inflammatory disorder that mainly targets the joints. Several lines of evidence have pointed to B cell function as a critical factor in the development of RA. B cells play several roles in th...

Full description

Saved in:
Bibliographic Details
Published in:Clinical reviews in allergy & immunology 2012-12, Vol.43 (3), p.281-291
Main Authors: Moura, Rita, Silva Graca, Luis Ricardo, Fonseca, João
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c529t-cf50e32dc0660c9cb174c0848101e65188e481ae29975ee99d2a31b44435d1913
cites cdi_FETCH-LOGICAL-c529t-cf50e32dc0660c9cb174c0848101e65188e481ae29975ee99d2a31b44435d1913
container_end_page 291
container_issue 3
container_start_page 281
container_title Clinical reviews in allergy & immunology
container_volume 43
creator Moura, Rita
Silva Graca, Luis Ricardo
Fonseca, João
description © Springer Science+Business Media, LLC 2012 Rheumatoid arthritis (RA) is a chronic, systemic immune-mediated inflammatory disorder that mainly targets the joints. Several lines of evidence have pointed to B cell function as a critical factor in the development of RA. B cells play several roles in the pathogenesis of RA, such as autoantibody production, antigen presentation and T cell activation, cytokine release, and ectopic lymphoid organogenesis. The success of B cell depletion therapy in RA further supports the relevance of these cells in RA progression. In addition, recent studies have also highlighted the B cell role in the first weeks of RA onset. The present article is a review focused in the immunopathogenic B cell-dependent mechanisms associated with RA development and chronicity and the importance of the recent discoveries documented in untreated very early RA patients with less than 6 weeks of disease duration.
doi_str_mv 10.1007/s12016-012-8318-y
format article
fullrecord <record><control><sourceid>gale_proqu</sourceid><recordid>TN_cdi_proquest_miscellaneous_1257762563</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A372555692</galeid><sourcerecordid>A372555692</sourcerecordid><originalsourceid>FETCH-LOGICAL-c529t-cf50e32dc0660c9cb174c0848101e65188e481ae29975ee99d2a31b44435d1913</originalsourceid><addsrcrecordid>eNqFkluL1TAUhYsozkV_gC9SEcSXjtm5Nm8eh_ECA4KMzyEn3Z1m6GmOSSqcf29KR50RUfKQzc63dljJqqpnQM6AEPUmASUgGwK0aRm0zeFBdQxC6IZQqR6WmrSkIYLro-okpRtCKGmZflwdUapAaSaOq7dXoX5Xh1hPIdd5qfOAtQtTN7tc2qGvvww472wOvqs3MQ_RZ5-Kwg2YcrRPqke9HRM-vd1Pq6_vL67OPzaXnz98Ot9cNk5QnRvXC4KMdo5ISZx2W1DckZa3QAClgLbFUlukWiuBqHVHLYMt55yJDjSw0-r1Oncfw7e5XG12PjkcRzthmJMBKpSSVEj2fxQEECZBqoK-_AO9CXOcipFCcdYqXh74N3VtRzR-6kMx7pahZsMUFUJITQt19heqrA53vrwo9r707wle3REMaMc8pDDO2Ycp3QdhBV0MKUXszT76nY0HA8QsSTBrEkxJglmSYA5F8_zW2bzdYfdL8fPrC0BXIJWj6RrjHev_mPpiFUVn7d5E_O5TtouCCzBcawHsB1kYwu8</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1143874016</pqid></control><display><type>article</type><title>To B or not to B the conductor of Rheumatoid Arthritis orchestra</title><source>Springer Nature:Jisc Collections:Springer Nature Read and Publish 2023-2025: Springer Reading List</source><creator>Moura, Rita ; Silva Graca, Luis Ricardo ; Fonseca, João</creator><creatorcontrib>Moura, Rita ; Silva Graca, Luis Ricardo ; Fonseca, João</creatorcontrib><description>© Springer Science+Business Media, LLC 2012 Rheumatoid arthritis (RA) is a chronic, systemic immune-mediated inflammatory disorder that mainly targets the joints. Several lines of evidence have pointed to B cell function as a critical factor in the development of RA. B cells play several roles in the pathogenesis of RA, such as autoantibody production, antigen presentation and T cell activation, cytokine release, and ectopic lymphoid organogenesis. The success of B cell depletion therapy in RA further supports the relevance of these cells in RA progression. In addition, recent studies have also highlighted the B cell role in the first weeks of RA onset. The present article is a review focused in the immunopathogenic B cell-dependent mechanisms associated with RA development and chronicity and the importance of the recent discoveries documented in untreated very early RA patients with less than 6 weeks of disease duration.</description><identifier>ISSN: 1080-0549</identifier><identifier>EISSN: 1559-0267</identifier><identifier>DOI: 10.1007/s12016-012-8318-y</identifier><identifier>PMID: 22717935</identifier><language>eng</language><publisher>New York: Springer Nature</publisher><subject>Allergology ; Antigen presentation ; Arthritis ; Arthritis, Rheumatoid - etiology ; Arthritis, Rheumatoid - immunology ; Arthritis, Rheumatoid - pathology ; Autoantibodies ; Autoimmunity ; B cells ; B-Lymphocytes - immunology ; B-Lymphocytes - pathology ; Cell activation ; Conductors ; Cytokines ; Developmental biology ; Humans ; Immunology ; Inflammatory diseases ; Internal Medicine ; Joint diseases ; Lymphocytes B ; Lymphocytes T ; Medicine ; Medicine &amp; Public Health ; Organogenesis ; Reviews ; Rheumatoid arthritis ; Rheumatoid factor ; Rituximab ; Synovium ; T cells</subject><ispartof>Clinical reviews in allergy &amp; immunology, 2012-12, Vol.43 (3), p.281-291</ispartof><rights>Springer Science+Business Media, LLC 2012</rights><rights>COPYRIGHT 2012 Springer</rights><rights>Springer Science+Business Media New York 2012</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c529t-cf50e32dc0660c9cb174c0848101e65188e481ae29975ee99d2a31b44435d1913</citedby><cites>FETCH-LOGICAL-c529t-cf50e32dc0660c9cb174c0848101e65188e481ae29975ee99d2a31b44435d1913</cites><orcidid>0000-0003-1432-3671 ; 0000-0002-9685-6924 ; 0000-0001-6935-8500</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22717935$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Moura, Rita</creatorcontrib><creatorcontrib>Silva Graca, Luis Ricardo</creatorcontrib><creatorcontrib>Fonseca, João</creatorcontrib><title>To B or not to B the conductor of Rheumatoid Arthritis orchestra</title><title>Clinical reviews in allergy &amp; immunology</title><addtitle>Clinic Rev Allerg Immunol</addtitle><addtitle>Clin Rev Allergy Immunol</addtitle><description>© Springer Science+Business Media, LLC 2012 Rheumatoid arthritis (RA) is a chronic, systemic immune-mediated inflammatory disorder that mainly targets the joints. Several lines of evidence have pointed to B cell function as a critical factor in the development of RA. B cells play several roles in the pathogenesis of RA, such as autoantibody production, antigen presentation and T cell activation, cytokine release, and ectopic lymphoid organogenesis. The success of B cell depletion therapy in RA further supports the relevance of these cells in RA progression. In addition, recent studies have also highlighted the B cell role in the first weeks of RA onset. The present article is a review focused in the immunopathogenic B cell-dependent mechanisms associated with RA development and chronicity and the importance of the recent discoveries documented in untreated very early RA patients with less than 6 weeks of disease duration.</description><subject>Allergology</subject><subject>Antigen presentation</subject><subject>Arthritis</subject><subject>Arthritis, Rheumatoid - etiology</subject><subject>Arthritis, Rheumatoid - immunology</subject><subject>Arthritis, Rheumatoid - pathology</subject><subject>Autoantibodies</subject><subject>Autoimmunity</subject><subject>B cells</subject><subject>B-Lymphocytes - immunology</subject><subject>B-Lymphocytes - pathology</subject><subject>Cell activation</subject><subject>Conductors</subject><subject>Cytokines</subject><subject>Developmental biology</subject><subject>Humans</subject><subject>Immunology</subject><subject>Inflammatory diseases</subject><subject>Internal Medicine</subject><subject>Joint diseases</subject><subject>Lymphocytes B</subject><subject>Lymphocytes T</subject><subject>Medicine</subject><subject>Medicine &amp; Public Health</subject><subject>Organogenesis</subject><subject>Reviews</subject><subject>Rheumatoid arthritis</subject><subject>Rheumatoid factor</subject><subject>Rituximab</subject><subject>Synovium</subject><subject>T cells</subject><issn>1080-0549</issn><issn>1559-0267</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><recordid>eNqFkluL1TAUhYsozkV_gC9SEcSXjtm5Nm8eh_ECA4KMzyEn3Z1m6GmOSSqcf29KR50RUfKQzc63dljJqqpnQM6AEPUmASUgGwK0aRm0zeFBdQxC6IZQqR6WmrSkIYLro-okpRtCKGmZflwdUapAaSaOq7dXoX5Xh1hPIdd5qfOAtQtTN7tc2qGvvww472wOvqs3MQ_RZ5-Kwg2YcrRPqke9HRM-vd1Pq6_vL67OPzaXnz98Ot9cNk5QnRvXC4KMdo5ISZx2W1DckZa3QAClgLbFUlukWiuBqHVHLYMt55yJDjSw0-r1Oncfw7e5XG12PjkcRzthmJMBKpSSVEj2fxQEECZBqoK-_AO9CXOcipFCcdYqXh74N3VtRzR-6kMx7pahZsMUFUJITQt19heqrA53vrwo9r707wle3REMaMc8pDDO2Ycp3QdhBV0MKUXszT76nY0HA8QsSTBrEkxJglmSYA5F8_zW2bzdYfdL8fPrC0BXIJWj6RrjHev_mPpiFUVn7d5E_O5TtouCCzBcawHsB1kYwu8</recordid><startdate>20121201</startdate><enddate>20121201</enddate><creator>Moura, Rita</creator><creator>Silva Graca, Luis Ricardo</creator><creator>Fonseca, João</creator><general>Springer Nature</general><general>Humana Press Inc</general><general>Springer</general><general>Springer Nature B.V</general><scope>RCLKO</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7T5</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>PHGZM</scope><scope>PHGZT</scope><scope>PJZUB</scope><scope>PKEHL</scope><scope>PPXIY</scope><scope>PQEST</scope><scope>PQGLB</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-1432-3671</orcidid><orcidid>https://orcid.org/0000-0002-9685-6924</orcidid><orcidid>https://orcid.org/0000-0001-6935-8500</orcidid></search><sort><creationdate>20121201</creationdate><title>To B or not to B the conductor of Rheumatoid Arthritis orchestra</title><author>Moura, Rita ; Silva Graca, Luis Ricardo ; Fonseca, João</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c529t-cf50e32dc0660c9cb174c0848101e65188e481ae29975ee99d2a31b44435d1913</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Allergology</topic><topic>Antigen presentation</topic><topic>Arthritis</topic><topic>Arthritis, Rheumatoid - etiology</topic><topic>Arthritis, Rheumatoid - immunology</topic><topic>Arthritis, Rheumatoid - pathology</topic><topic>Autoantibodies</topic><topic>Autoimmunity</topic><topic>B cells</topic><topic>B-Lymphocytes - immunology</topic><topic>B-Lymphocytes - pathology</topic><topic>Cell activation</topic><topic>Conductors</topic><topic>Cytokines</topic><topic>Developmental biology</topic><topic>Humans</topic><topic>Immunology</topic><topic>Inflammatory diseases</topic><topic>Internal Medicine</topic><topic>Joint diseases</topic><topic>Lymphocytes B</topic><topic>Lymphocytes T</topic><topic>Medicine</topic><topic>Medicine &amp; Public Health</topic><topic>Organogenesis</topic><topic>Reviews</topic><topic>Rheumatoid arthritis</topic><topic>Rheumatoid factor</topic><topic>Rituximab</topic><topic>Synovium</topic><topic>T cells</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Moura, Rita</creatorcontrib><creatorcontrib>Silva Graca, Luis Ricardo</creatorcontrib><creatorcontrib>Fonseca, João</creatorcontrib><collection>RCAAP open access repository</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Immunology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science Database</collection><collection>ProQuest Central (New)</collection><collection>ProQuest One Academic (New)</collection><collection>ProQuest Health &amp; Medical Research Collection</collection><collection>ProQuest One Academic Middle East (New)</collection><collection>ProQuest One Health &amp; Nursing</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Applied &amp; Life Sciences</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><jtitle>Clinical reviews in allergy &amp; immunology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Moura, Rita</au><au>Silva Graca, Luis Ricardo</au><au>Fonseca, João</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>To B or not to B the conductor of Rheumatoid Arthritis orchestra</atitle><jtitle>Clinical reviews in allergy &amp; immunology</jtitle><stitle>Clinic Rev Allerg Immunol</stitle><addtitle>Clin Rev Allergy Immunol</addtitle><date>2012-12-01</date><risdate>2012</risdate><volume>43</volume><issue>3</issue><spage>281</spage><epage>291</epage><pages>281-291</pages><issn>1080-0549</issn><eissn>1559-0267</eissn><abstract>© Springer Science+Business Media, LLC 2012 Rheumatoid arthritis (RA) is a chronic, systemic immune-mediated inflammatory disorder that mainly targets the joints. Several lines of evidence have pointed to B cell function as a critical factor in the development of RA. B cells play several roles in the pathogenesis of RA, such as autoantibody production, antigen presentation and T cell activation, cytokine release, and ectopic lymphoid organogenesis. The success of B cell depletion therapy in RA further supports the relevance of these cells in RA progression. In addition, recent studies have also highlighted the B cell role in the first weeks of RA onset. The present article is a review focused in the immunopathogenic B cell-dependent mechanisms associated with RA development and chronicity and the importance of the recent discoveries documented in untreated very early RA patients with less than 6 weeks of disease duration.</abstract><cop>New York</cop><pub>Springer Nature</pub><pmid>22717935</pmid><doi>10.1007/s12016-012-8318-y</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0003-1432-3671</orcidid><orcidid>https://orcid.org/0000-0002-9685-6924</orcidid><orcidid>https://orcid.org/0000-0001-6935-8500</orcidid><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 1080-0549
ispartof Clinical reviews in allergy & immunology, 2012-12, Vol.43 (3), p.281-291
issn 1080-0549
1559-0267
language eng
recordid cdi_proquest_miscellaneous_1257762563
source Springer Nature:Jisc Collections:Springer Nature Read and Publish 2023-2025: Springer Reading List
subjects Allergology
Antigen presentation
Arthritis
Arthritis, Rheumatoid - etiology
Arthritis, Rheumatoid - immunology
Arthritis, Rheumatoid - pathology
Autoantibodies
Autoimmunity
B cells
B-Lymphocytes - immunology
B-Lymphocytes - pathology
Cell activation
Conductors
Cytokines
Developmental biology
Humans
Immunology
Inflammatory diseases
Internal Medicine
Joint diseases
Lymphocytes B
Lymphocytes T
Medicine
Medicine & Public Health
Organogenesis
Reviews
Rheumatoid arthritis
Rheumatoid factor
Rituximab
Synovium
T cells
title To B or not to B the conductor of Rheumatoid Arthritis orchestra
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-23T21%3A05%3A50IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_proqu&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=To%20B%20or%20not%20to%20B%20the%20conductor%20of%20Rheumatoid%20Arthritis%20orchestra&rft.jtitle=Clinical%20reviews%20in%20allergy%20&%20immunology&rft.au=Moura,%20Rita&rft.date=2012-12-01&rft.volume=43&rft.issue=3&rft.spage=281&rft.epage=291&rft.pages=281-291&rft.issn=1080-0549&rft.eissn=1559-0267&rft_id=info:doi/10.1007/s12016-012-8318-y&rft_dat=%3Cgale_proqu%3EA372555692%3C/gale_proqu%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c529t-cf50e32dc0660c9cb174c0848101e65188e481ae29975ee99d2a31b44435d1913%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=1143874016&rft_id=info:pmid/22717935&rft_galeid=A372555692&rfr_iscdi=true