Enrichment of malondialdehyde-acetaldehyde antibody in the rheumatoid arthritis joint
To characterize the expression of malondialdehdye-acetaldehyde (MAA) adducts and anti-MAA antibody in articular tissues and serum of patients with RA. Paired sera and SF were examined from 29 RA and 13 OA patients. Anti-MAA antibody, RF, ACPA and total immunoglobulin were quantified. SF-serum measur...
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Veröffentlicht in: | Rheumatology (Oxford, England) England), 2017-10, Vol.56 (10), p.1794-1803 |
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creator | Mikuls, Ted R Duryee, Michael J Rahman, Rafid Anderson, Daniel R Sayles, Harlan R Hollins, Andrew Michaud, Kaleb Wolfe, Frederick Thiele, Geoffrey E Sokolove, Jeremy Robinson, William H Lingampalli, Nithya Nicholas, Anthony P Talmon, Geoffrey A Su, Kaihong Zimmerman, Matthew C Klassen, Lynell W Thiele, Geoffrey M |
description | To characterize the expression of malondialdehdye-acetaldehyde (MAA) adducts and anti-MAA antibody in articular tissues and serum of patients with RA.
Paired sera and SF were examined from 29 RA and 13 OA patients. Anti-MAA antibody, RF, ACPA and total immunoglobulin were quantified. SF-serum measures were compared within and between disease groups. The presence and co-localization of MAA, citrulline and select leukocyte antigens in RA and OA synovial tissues were examined using immunohistochemistry.
Circulating and SF anti-MAA antibody concentrations were higher in RA vs OA by 1.5- to 5-fold. IgG (P < 0.001), IgM (P = 0.006) and IgA (P = 0.036) anti-MAA antibodies were higher in paired RA SF than serum, differences not observed for total immunoglobulin, RF or ACPA. In RA synovial tissues, co-localization of MAA with citrulline and CD19+ or CD27+ B cells was demonstrated and was much higher in magnitude than MAA or citrulline co-localization with T cells, monocytes, macrophages or dendritic cells (P < 0.01).
Anti-MAA antibodies are present in higher concentrations in the RA joint compared with sera, a finding not observed for other disease-related autoantibodies. Co-localization of MAA and citrulline with mature B cells, coupled with the local enrichment of anti-MAA immune responses, implicates MAA-adduct formation in local autoantibody production. |
doi_str_mv | 10.1093/rheumatology/kex212 |
format | Article |
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Paired sera and SF were examined from 29 RA and 13 OA patients. Anti-MAA antibody, RF, ACPA and total immunoglobulin were quantified. SF-serum measures were compared within and between disease groups. The presence and co-localization of MAA, citrulline and select leukocyte antigens in RA and OA synovial tissues were examined using immunohistochemistry.
Circulating and SF anti-MAA antibody concentrations were higher in RA vs OA by 1.5- to 5-fold. IgG (P < 0.001), IgM (P = 0.006) and IgA (P = 0.036) anti-MAA antibodies were higher in paired RA SF than serum, differences not observed for total immunoglobulin, RF or ACPA. In RA synovial tissues, co-localization of MAA with citrulline and CD19+ or CD27+ B cells was demonstrated and was much higher in magnitude than MAA or citrulline co-localization with T cells, monocytes, macrophages or dendritic cells (P < 0.01).
Anti-MAA antibodies are present in higher concentrations in the RA joint compared with sera, a finding not observed for other disease-related autoantibodies. Co-localization of MAA and citrulline with mature B cells, coupled with the local enrichment of anti-MAA immune responses, implicates MAA-adduct formation in local autoantibody production.</description><identifier>ISSN: 1462-0324</identifier><identifier>EISSN: 1462-0332</identifier><identifier>DOI: 10.1093/rheumatology/kex212</identifier><identifier>PMID: 28957552</identifier><language>eng</language><publisher>England: Oxford University Press</publisher><subject>Acetaldehyde - immunology ; Aged ; Arthritis, Rheumatoid - blood ; Arthritis, Rheumatoid - immunology ; Autoantibodies - analysis ; Basic and Translational Science ; Case-Control Studies ; Female ; Humans ; Immunohistochemistry ; Joints - immunology ; Male ; Malondialdehyde - immunology ; Middle Aged ; Osteoarthritis - blood ; Osteoarthritis - immunology ; Rheumatoid Factor - blood ; Synovial Fluid - immunology</subject><ispartof>Rheumatology (Oxford, England), 2017-10, Vol.56 (10), p.1794-1803</ispartof><rights>The Author 2017. Published by Oxford University Press on behalf of the British Society for Rheumatology. All rights reserved. For Permissions, please email: journals.permissions@oup.com</rights><rights>The Author 2017. Published by Oxford University Press on behalf of the British Society for Rheumatology. All rights reserved. For Permissions, please email: journals.permissions@oup.com 2017</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c405t-6947903aa4b135c8f2f8b699714c7f3f4e74aa5700563a02b170bb933a8eb75b3</citedby><cites>FETCH-LOGICAL-c405t-6947903aa4b135c8f2f8b699714c7f3f4e74aa5700563a02b170bb933a8eb75b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28957552$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mikuls, Ted R</creatorcontrib><creatorcontrib>Duryee, Michael J</creatorcontrib><creatorcontrib>Rahman, Rafid</creatorcontrib><creatorcontrib>Anderson, Daniel R</creatorcontrib><creatorcontrib>Sayles, Harlan R</creatorcontrib><creatorcontrib>Hollins, Andrew</creatorcontrib><creatorcontrib>Michaud, Kaleb</creatorcontrib><creatorcontrib>Wolfe, Frederick</creatorcontrib><creatorcontrib>Thiele, Geoffrey E</creatorcontrib><creatorcontrib>Sokolove, Jeremy</creatorcontrib><creatorcontrib>Robinson, William H</creatorcontrib><creatorcontrib>Lingampalli, Nithya</creatorcontrib><creatorcontrib>Nicholas, Anthony P</creatorcontrib><creatorcontrib>Talmon, Geoffrey A</creatorcontrib><creatorcontrib>Su, Kaihong</creatorcontrib><creatorcontrib>Zimmerman, Matthew C</creatorcontrib><creatorcontrib>Klassen, Lynell W</creatorcontrib><creatorcontrib>Thiele, Geoffrey M</creatorcontrib><title>Enrichment of malondialdehyde-acetaldehyde antibody in the rheumatoid arthritis joint</title><title>Rheumatology (Oxford, England)</title><addtitle>Rheumatology (Oxford)</addtitle><description>To characterize the expression of malondialdehdye-acetaldehyde (MAA) adducts and anti-MAA antibody in articular tissues and serum of patients with RA.
Paired sera and SF were examined from 29 RA and 13 OA patients. Anti-MAA antibody, RF, ACPA and total immunoglobulin were quantified. SF-serum measures were compared within and between disease groups. The presence and co-localization of MAA, citrulline and select leukocyte antigens in RA and OA synovial tissues were examined using immunohistochemistry.
Circulating and SF anti-MAA antibody concentrations were higher in RA vs OA by 1.5- to 5-fold. IgG (P < 0.001), IgM (P = 0.006) and IgA (P = 0.036) anti-MAA antibodies were higher in paired RA SF than serum, differences not observed for total immunoglobulin, RF or ACPA. In RA synovial tissues, co-localization of MAA with citrulline and CD19+ or CD27+ B cells was demonstrated and was much higher in magnitude than MAA or citrulline co-localization with T cells, monocytes, macrophages or dendritic cells (P < 0.01).
Anti-MAA antibodies are present in higher concentrations in the RA joint compared with sera, a finding not observed for other disease-related autoantibodies. Co-localization of MAA and citrulline with mature B cells, coupled with the local enrichment of anti-MAA immune responses, implicates MAA-adduct formation in local autoantibody production.</description><subject>Acetaldehyde - immunology</subject><subject>Aged</subject><subject>Arthritis, Rheumatoid - blood</subject><subject>Arthritis, Rheumatoid - immunology</subject><subject>Autoantibodies - analysis</subject><subject>Basic and Translational Science</subject><subject>Case-Control Studies</subject><subject>Female</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>Joints - immunology</subject><subject>Male</subject><subject>Malondialdehyde - immunology</subject><subject>Middle Aged</subject><subject>Osteoarthritis - blood</subject><subject>Osteoarthritis - immunology</subject><subject>Rheumatoid Factor - blood</subject><subject>Synovial Fluid - immunology</subject><issn>1462-0324</issn><issn>1462-0332</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVUctOwzAQtBCIlsIXIKEcuYT62cQXJFSVh1SJCz1b68RpXJK42C6if09QHyqn3dXOzM5qELol-IFgyca-NpsWomvccjv-ND-U0DM0JHxCU8wYPT_2lA_QVQgrjLEgLL9EA5pLkQlBh2gx67wt6tZ0MXFV0kLjutJCU5p6W5oUChMPQwJdtNqV28R2SaxNcjBgywR8rL2NNiQrZ7t4jS4qaIK52dcRWjzPPqav6fz95W36NE8LjkVMJ5JnEjMArgkTRV7RKtcTKTPCi6xiFTcZBxBZ73vCAFNNMqy1ZAxyozOh2Qg97nTXG92asui_8NCotbct-K1yYNX_TWdrtXTfSuQC54z1Avd7Ae--NiZE1dpQmKaBzrhNUERyQSnJJe-hbActvAvBm-p4hmD1F4g6DUTtAulZd6cOj5xDAuwXZTqOgA</recordid><startdate>20171001</startdate><enddate>20171001</enddate><creator>Mikuls, Ted R</creator><creator>Duryee, Michael J</creator><creator>Rahman, Rafid</creator><creator>Anderson, Daniel R</creator><creator>Sayles, Harlan R</creator><creator>Hollins, Andrew</creator><creator>Michaud, Kaleb</creator><creator>Wolfe, Frederick</creator><creator>Thiele, Geoffrey E</creator><creator>Sokolove, Jeremy</creator><creator>Robinson, William H</creator><creator>Lingampalli, Nithya</creator><creator>Nicholas, Anthony P</creator><creator>Talmon, Geoffrey A</creator><creator>Su, Kaihong</creator><creator>Zimmerman, Matthew C</creator><creator>Klassen, Lynell W</creator><creator>Thiele, Geoffrey M</creator><general>Oxford University Press</general><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>7X8</scope><scope>5PM</scope></search><sort><creationdate>20171001</creationdate><title>Enrichment of malondialdehyde-acetaldehyde antibody in the rheumatoid arthritis joint</title><author>Mikuls, Ted R ; Duryee, Michael J ; Rahman, Rafid ; Anderson, Daniel R ; Sayles, Harlan R ; Hollins, Andrew ; Michaud, Kaleb ; Wolfe, Frederick ; Thiele, Geoffrey E ; Sokolove, Jeremy ; Robinson, William H ; Lingampalli, Nithya ; Nicholas, Anthony P ; Talmon, Geoffrey A ; Su, Kaihong ; Zimmerman, Matthew C ; Klassen, Lynell W ; Thiele, Geoffrey M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c405t-6947903aa4b135c8f2f8b699714c7f3f4e74aa5700563a02b170bb933a8eb75b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Acetaldehyde - immunology</topic><topic>Aged</topic><topic>Arthritis, Rheumatoid - blood</topic><topic>Arthritis, Rheumatoid - immunology</topic><topic>Autoantibodies - analysis</topic><topic>Basic and Translational Science</topic><topic>Case-Control Studies</topic><topic>Female</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>Joints - immunology</topic><topic>Male</topic><topic>Malondialdehyde - immunology</topic><topic>Middle Aged</topic><topic>Osteoarthritis - blood</topic><topic>Osteoarthritis - immunology</topic><topic>Rheumatoid Factor - blood</topic><topic>Synovial Fluid - immunology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mikuls, Ted R</creatorcontrib><creatorcontrib>Duryee, Michael J</creatorcontrib><creatorcontrib>Rahman, Rafid</creatorcontrib><creatorcontrib>Anderson, Daniel R</creatorcontrib><creatorcontrib>Sayles, Harlan R</creatorcontrib><creatorcontrib>Hollins, Andrew</creatorcontrib><creatorcontrib>Michaud, Kaleb</creatorcontrib><creatorcontrib>Wolfe, Frederick</creatorcontrib><creatorcontrib>Thiele, Geoffrey E</creatorcontrib><creatorcontrib>Sokolove, Jeremy</creatorcontrib><creatorcontrib>Robinson, William H</creatorcontrib><creatorcontrib>Lingampalli, Nithya</creatorcontrib><creatorcontrib>Nicholas, Anthony P</creatorcontrib><creatorcontrib>Talmon, Geoffrey A</creatorcontrib><creatorcontrib>Su, Kaihong</creatorcontrib><creatorcontrib>Zimmerman, Matthew C</creatorcontrib><creatorcontrib>Klassen, Lynell W</creatorcontrib><creatorcontrib>Thiele, Geoffrey M</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Rheumatology (Oxford, England)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mikuls, Ted R</au><au>Duryee, Michael J</au><au>Rahman, Rafid</au><au>Anderson, Daniel R</au><au>Sayles, Harlan R</au><au>Hollins, Andrew</au><au>Michaud, Kaleb</au><au>Wolfe, Frederick</au><au>Thiele, Geoffrey E</au><au>Sokolove, Jeremy</au><au>Robinson, William H</au><au>Lingampalli, Nithya</au><au>Nicholas, Anthony P</au><au>Talmon, Geoffrey A</au><au>Su, Kaihong</au><au>Zimmerman, Matthew C</au><au>Klassen, Lynell W</au><au>Thiele, Geoffrey M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Enrichment of malondialdehyde-acetaldehyde antibody in the rheumatoid arthritis joint</atitle><jtitle>Rheumatology (Oxford, England)</jtitle><addtitle>Rheumatology (Oxford)</addtitle><date>2017-10-01</date><risdate>2017</risdate><volume>56</volume><issue>10</issue><spage>1794</spage><epage>1803</epage><pages>1794-1803</pages><issn>1462-0324</issn><eissn>1462-0332</eissn><abstract>To characterize the expression of malondialdehdye-acetaldehyde (MAA) adducts and anti-MAA antibody in articular tissues and serum of patients with RA.
Paired sera and SF were examined from 29 RA and 13 OA patients. Anti-MAA antibody, RF, ACPA and total immunoglobulin were quantified. SF-serum measures were compared within and between disease groups. The presence and co-localization of MAA, citrulline and select leukocyte antigens in RA and OA synovial tissues were examined using immunohistochemistry.
Circulating and SF anti-MAA antibody concentrations were higher in RA vs OA by 1.5- to 5-fold. IgG (P < 0.001), IgM (P = 0.006) and IgA (P = 0.036) anti-MAA antibodies were higher in paired RA SF than serum, differences not observed for total immunoglobulin, RF or ACPA. In RA synovial tissues, co-localization of MAA with citrulline and CD19+ or CD27+ B cells was demonstrated and was much higher in magnitude than MAA or citrulline co-localization with T cells, monocytes, macrophages or dendritic cells (P < 0.01).
Anti-MAA antibodies are present in higher concentrations in the RA joint compared with sera, a finding not observed for other disease-related autoantibodies. Co-localization of MAA and citrulline with mature B cells, coupled with the local enrichment of anti-MAA immune responses, implicates MAA-adduct formation in local autoantibody production.</abstract><cop>England</cop><pub>Oxford University Press</pub><pmid>28957552</pmid><doi>10.1093/rheumatology/kex212</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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source | Oxford University Press Journals All Titles (1996-Current); MEDLINE; Alma/SFX Local Collection |
subjects | Acetaldehyde - immunology Aged Arthritis, Rheumatoid - blood Arthritis, Rheumatoid - immunology Autoantibodies - analysis Basic and Translational Science Case-Control Studies Female Humans Immunohistochemistry Joints - immunology Male Malondialdehyde - immunology Middle Aged Osteoarthritis - blood Osteoarthritis - immunology Rheumatoid Factor - blood Synovial Fluid - immunology |
title | Enrichment of malondialdehyde-acetaldehyde antibody in the rheumatoid arthritis joint |
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