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Male microchimerism and HLA compatibility in French women with sclerodema: a different profile in limited and diffuse subset
Objectives. Male microchimerism (Mc) persisting from pregnancy has been found at greater frequencies and/or higher quantities in women with scleroderma (SSc) compared with controls, suggesting a possible role in disease development. Moreover, women with an HLA-compatible child have a higher risk to...
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Published in: | Rheumatology (Oxford, England) England), 2009-04, Vol.48 (4), p.363-366 |
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creator | Rak, Justyna M. Pagni, Philippe P. Tiev, Kiet Allanore, Yannick Farge, Dominique Harlé, Jean-Robert Launay, David Hachulla, Eric Didelot, Rémi Cabane, Jean Kahan, André Martin, Marielle Granel, Brigitte Roudier, Jean Lambert, Nathalie C. |
description | Objectives. Male microchimerism (Mc) persisting from pregnancy has been found at greater frequencies and/or higher quantities in women with scleroderma (SSc) compared with controls, suggesting a possible role in disease development. Moreover, women with an HLA-compatible child have a higher risk to develop SSc. We tested the hypothesis, on our French SSc cohort, that women with lcSSc and dcSSc, two distinct clinical subsets, have a different profile in terms of Mc and HLA compatibility in families. Methods. We studied 98 women (52 lcSSc and 46 dcSSc) for male Mc, by real-time PCR, in their whole blood and/or peripheral blood mononuclear cells (PBMC). Similarly, 91 matched healthy women were analysed. Complete HLA-DRB1 typing was obtained for 58 SSc and 68 control families (proband/children). Results. Women with lcSSc (N = 50) had male Mc more often in their whole blood than women with dcSSc (N = 40, 20 vs 5%, P = 0.038), but not significantly more than controls. By contrast, women with dcSSc (N = 36) hold Mc more often in PBMC (25 vs 9%), but not significantly and have greater quantities than controls (N = 82, P = 0.048). This contrast is also visible in feto-maternal HLA-DRB1 compatibility, which was increased only among women with lcSSc (N = 33) compared with controls (N = 68, P = 0.003). Conclusion. For the first time, we showed that women with lcSSc and dcSSc hold male Mc in different blood compartments. Furthermore, a distinct pattern between the two SSc subtypes is observed for feto-maternal HLA-DRB1 compatibility. These results suggest a different mechanism behind each type of disease. |
doi_str_mv | 10.1093/rheumatology/ken505 |
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Male microchimerism (Mc) persisting from pregnancy has been found at greater frequencies and/or higher quantities in women with scleroderma (SSc) compared with controls, suggesting a possible role in disease development. Moreover, women with an HLA-compatible child have a higher risk to develop SSc. We tested the hypothesis, on our French SSc cohort, that women with lcSSc and dcSSc, two distinct clinical subsets, have a different profile in terms of Mc and HLA compatibility in families. Methods. We studied 98 women (52 lcSSc and 46 dcSSc) for male Mc, by real-time PCR, in their whole blood and/or peripheral blood mononuclear cells (PBMC). Similarly, 91 matched healthy women were analysed. Complete HLA-DRB1 typing was obtained for 58 SSc and 68 control families (proband/children). Results. Women with lcSSc (N = 50) had male Mc more often in their whole blood than women with dcSSc (N = 40, 20 vs 5%, P = 0.038), but not significantly more than controls. By contrast, women with dcSSc (N = 36) hold Mc more often in PBMC (25 vs 9%), but not significantly and have greater quantities than controls (N = 82, P = 0.048). This contrast is also visible in feto-maternal HLA-DRB1 compatibility, which was increased only among women with lcSSc (N = 33) compared with controls (N = 68, P = 0.003). Conclusion. For the first time, we showed that women with lcSSc and dcSSc hold male Mc in different blood compartments. Furthermore, a distinct pattern between the two SSc subtypes is observed for feto-maternal HLA-DRB1 compatibility. These results suggest a different mechanism behind each type of disease.</description><identifier>ISSN: 1462-0324</identifier><identifier>EISSN: 1462-0332</identifier><identifier>DOI: 10.1093/rheumatology/ken505</identifier><identifier>PMID: 19208687</identifier><identifier>CODEN: BJRHDF</identifier><language>eng</language><publisher>Oxford: Oxford University Press</publisher><subject>Adolescent ; Adult ; Aged ; Biological and medical sciences ; Blood ; Case-Control Studies ; Child ; Chimerism ; Diffuse cutaneous scleroderma ; Diseases of the osteoarticular system ; Female ; Histocompatibility ; Histocompatibility Testing ; HLA-DR Antigens ; HLA-DRB1 Chains ; Humans ; Limited cutaneous scleroderma ; Male ; Medical sciences ; Microchimerism ; Middle Aged ; Mothers ; Peripheral blood mononuclear cells ; Pregnancy - genetics ; Pregnancy - immunology ; Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis ; Scleroderma, Diffuse - genetics ; Scleroderma, Limited - genetics ; Scleroderma, Systemic - genetics ; Scleroderma, Systemic - immunology ; Y-chromosome ; Young Adult</subject><ispartof>Rheumatology (Oxford, England), 2009-04, Vol.48 (4), p.363-366</ispartof><rights>The Author 2009. Published by Oxford University Press on behalf of the British Society for Rheumatology. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org 2009</rights><rights>2009 INIST-CNRS</rights><rights>The Author 2009. Published by Oxford University Press on behalf of the British Society for Rheumatology. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c482t-ccd6bad66a73ac45c93f1261108c8950a242bb1efbcd11076e033f5f4b089a593</citedby><cites>FETCH-LOGICAL-c482t-ccd6bad66a73ac45c93f1261108c8950a242bb1efbcd11076e033f5f4b089a593</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=21336420$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19208687$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Rak, Justyna M.</creatorcontrib><creatorcontrib>Pagni, Philippe P.</creatorcontrib><creatorcontrib>Tiev, Kiet</creatorcontrib><creatorcontrib>Allanore, Yannick</creatorcontrib><creatorcontrib>Farge, Dominique</creatorcontrib><creatorcontrib>Harlé, Jean-Robert</creatorcontrib><creatorcontrib>Launay, David</creatorcontrib><creatorcontrib>Hachulla, Eric</creatorcontrib><creatorcontrib>Didelot, Rémi</creatorcontrib><creatorcontrib>Cabane, Jean</creatorcontrib><creatorcontrib>Kahan, André</creatorcontrib><creatorcontrib>Martin, Marielle</creatorcontrib><creatorcontrib>Granel, Brigitte</creatorcontrib><creatorcontrib>Roudier, Jean</creatorcontrib><creatorcontrib>Lambert, Nathalie C.</creatorcontrib><title>Male microchimerism and HLA compatibility in French women with sclerodema: a different profile in limited and diffuse subset</title><title>Rheumatology (Oxford, England)</title><addtitle>Rheumatology (Oxford)</addtitle><description>Objectives. Male microchimerism (Mc) persisting from pregnancy has been found at greater frequencies and/or higher quantities in women with scleroderma (SSc) compared with controls, suggesting a possible role in disease development. Moreover, women with an HLA-compatible child have a higher risk to develop SSc. We tested the hypothesis, on our French SSc cohort, that women with lcSSc and dcSSc, two distinct clinical subsets, have a different profile in terms of Mc and HLA compatibility in families. Methods. We studied 98 women (52 lcSSc and 46 dcSSc) for male Mc, by real-time PCR, in their whole blood and/or peripheral blood mononuclear cells (PBMC). Similarly, 91 matched healthy women were analysed. Complete HLA-DRB1 typing was obtained for 58 SSc and 68 control families (proband/children). Results. Women with lcSSc (N = 50) had male Mc more often in their whole blood than women with dcSSc (N = 40, 20 vs 5%, P = 0.038), but not significantly more than controls. By contrast, women with dcSSc (N = 36) hold Mc more often in PBMC (25 vs 9%), but not significantly and have greater quantities than controls (N = 82, P = 0.048). This contrast is also visible in feto-maternal HLA-DRB1 compatibility, which was increased only among women with lcSSc (N = 33) compared with controls (N = 68, P = 0.003). Conclusion. For the first time, we showed that women with lcSSc and dcSSc hold male Mc in different blood compartments. Furthermore, a distinct pattern between the two SSc subtypes is observed for feto-maternal HLA-DRB1 compatibility. These results suggest a different mechanism behind each type of disease.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Biological and medical sciences</subject><subject>Blood</subject><subject>Case-Control Studies</subject><subject>Child</subject><subject>Chimerism</subject><subject>Diffuse cutaneous scleroderma</subject><subject>Diseases of the osteoarticular system</subject><subject>Female</subject><subject>Histocompatibility</subject><subject>Histocompatibility Testing</subject><subject>HLA-DR Antigens</subject><subject>HLA-DRB1 Chains</subject><subject>Humans</subject><subject>Limited cutaneous scleroderma</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Microchimerism</subject><subject>Middle Aged</subject><subject>Mothers</subject><subject>Peripheral blood mononuclear cells</subject><subject>Pregnancy - genetics</subject><subject>Pregnancy - immunology</subject><subject>Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis</subject><subject>Scleroderma, Diffuse - genetics</subject><subject>Scleroderma, Limited - genetics</subject><subject>Scleroderma, Systemic - genetics</subject><subject>Scleroderma, Systemic - immunology</subject><subject>Y-chromosome</subject><subject>Young Adult</subject><issn>1462-0324</issn><issn>1462-0332</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><recordid>eNqNkVtrFDEYhgdR7EF_gSBBsHfT5jDJzHhXltYVt4jgCW9CJvPFTTuZrEmGdsEfb-osW_HKq3yE532_w1sULwg-JbhlZ2ENk1PJD_7H9uwGRo75o-KQVIKWmDH6eF_T6qA4ivEaY8wJa54WB6SluBFNfVj8ulIDIGd18HptHQQbHVJjj5arc6S926hkOzvYtEV2RJcBRr1Gt97BiG5tWqOoBwi-B6feIIV6awxkJqFN8MZm5ywarLMJ-j-u98AUAcWpi5CeFU-MGiI8373HxefLi0-LZbn68Pbd4nxV6qqhqdS6F53qhVA1U7riumWGUEEIbnTTcqxoRbuOgOl0nz9rAXl_w03V4aZVvGXHxcnsm6f6OUFM0tmoYRjUCH6KUtSYY1zXGXz1D3jtpzDm2SRpueANr1iG2Azlm8UYwMhNsE6FrSRY3icj_05Gzslk1cud9dQ56B80uygy8HoHqKjVYIIatY17jhLGREVx5k5nzk-b_-xczgIbE9ztJSrc5MVZzeXy23dJv3z9uODviWTsN_PJvEQ</recordid><startdate>20090401</startdate><enddate>20090401</enddate><creator>Rak, Justyna M.</creator><creator>Pagni, Philippe P.</creator><creator>Tiev, Kiet</creator><creator>Allanore, Yannick</creator><creator>Farge, Dominique</creator><creator>Harlé, Jean-Robert</creator><creator>Launay, David</creator><creator>Hachulla, Eric</creator><creator>Didelot, Rémi</creator><creator>Cabane, Jean</creator><creator>Kahan, André</creator><creator>Martin, Marielle</creator><creator>Granel, Brigitte</creator><creator>Roudier, Jean</creator><creator>Lambert, Nathalie C.</creator><general>Oxford University Press</general><general>Oxford Publishing Limited (England)</general><scope>BSCLL</scope><scope>IQODW</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>7QP</scope><scope>K9.</scope><scope>NAPCQ</scope><scope>7X8</scope></search><sort><creationdate>20090401</creationdate><title>Male microchimerism and HLA compatibility in French women with sclerodema: a different profile in limited and diffuse subset</title><author>Rak, Justyna M. ; Pagni, Philippe P. ; Tiev, Kiet ; Allanore, Yannick ; Farge, Dominique ; Harlé, Jean-Robert ; Launay, David ; Hachulla, Eric ; Didelot, Rémi ; Cabane, Jean ; Kahan, André ; Martin, Marielle ; Granel, Brigitte ; Roudier, Jean ; Lambert, Nathalie C.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c482t-ccd6bad66a73ac45c93f1261108c8950a242bb1efbcd11076e033f5f4b089a593</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Aged</topic><topic>Biological and medical sciences</topic><topic>Blood</topic><topic>Case-Control Studies</topic><topic>Child</topic><topic>Chimerism</topic><topic>Diffuse cutaneous scleroderma</topic><topic>Diseases of the osteoarticular system</topic><topic>Female</topic><topic>Histocompatibility</topic><topic>Histocompatibility Testing</topic><topic>HLA-DR Antigens</topic><topic>HLA-DRB1 Chains</topic><topic>Humans</topic><topic>Limited cutaneous scleroderma</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Microchimerism</topic><topic>Middle Aged</topic><topic>Mothers</topic><topic>Peripheral blood mononuclear cells</topic><topic>Pregnancy - genetics</topic><topic>Pregnancy - immunology</topic><topic>Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis</topic><topic>Scleroderma, Diffuse - genetics</topic><topic>Scleroderma, Limited - genetics</topic><topic>Scleroderma, Systemic - genetics</topic><topic>Scleroderma, Systemic - immunology</topic><topic>Y-chromosome</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rak, Justyna M.</creatorcontrib><creatorcontrib>Pagni, Philippe P.</creatorcontrib><creatorcontrib>Tiev, Kiet</creatorcontrib><creatorcontrib>Allanore, Yannick</creatorcontrib><creatorcontrib>Farge, Dominique</creatorcontrib><creatorcontrib>Harlé, Jean-Robert</creatorcontrib><creatorcontrib>Launay, David</creatorcontrib><creatorcontrib>Hachulla, Eric</creatorcontrib><creatorcontrib>Didelot, Rémi</creatorcontrib><creatorcontrib>Cabane, Jean</creatorcontrib><creatorcontrib>Kahan, André</creatorcontrib><creatorcontrib>Martin, Marielle</creatorcontrib><creatorcontrib>Granel, Brigitte</creatorcontrib><creatorcontrib>Roudier, Jean</creatorcontrib><creatorcontrib>Lambert, Nathalie C.</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Premium</collection><collection>MEDLINE - Academic</collection><jtitle>Rheumatology (Oxford, England)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Rak, Justyna M.</au><au>Pagni, Philippe P.</au><au>Tiev, Kiet</au><au>Allanore, Yannick</au><au>Farge, Dominique</au><au>Harlé, Jean-Robert</au><au>Launay, David</au><au>Hachulla, Eric</au><au>Didelot, Rémi</au><au>Cabane, Jean</au><au>Kahan, André</au><au>Martin, Marielle</au><au>Granel, Brigitte</au><au>Roudier, Jean</au><au>Lambert, Nathalie C.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Male microchimerism and HLA compatibility in French women with sclerodema: a different profile in limited and diffuse subset</atitle><jtitle>Rheumatology (Oxford, England)</jtitle><addtitle>Rheumatology (Oxford)</addtitle><date>2009-04-01</date><risdate>2009</risdate><volume>48</volume><issue>4</issue><spage>363</spage><epage>366</epage><pages>363-366</pages><issn>1462-0324</issn><eissn>1462-0332</eissn><coden>BJRHDF</coden><abstract>Objectives. Male microchimerism (Mc) persisting from pregnancy has been found at greater frequencies and/or higher quantities in women with scleroderma (SSc) compared with controls, suggesting a possible role in disease development. Moreover, women with an HLA-compatible child have a higher risk to develop SSc. We tested the hypothesis, on our French SSc cohort, that women with lcSSc and dcSSc, two distinct clinical subsets, have a different profile in terms of Mc and HLA compatibility in families. Methods. We studied 98 women (52 lcSSc and 46 dcSSc) for male Mc, by real-time PCR, in their whole blood and/or peripheral blood mononuclear cells (PBMC). Similarly, 91 matched healthy women were analysed. Complete HLA-DRB1 typing was obtained for 58 SSc and 68 control families (proband/children). Results. Women with lcSSc (N = 50) had male Mc more often in their whole blood than women with dcSSc (N = 40, 20 vs 5%, P = 0.038), but not significantly more than controls. By contrast, women with dcSSc (N = 36) hold Mc more often in PBMC (25 vs 9%), but not significantly and have greater quantities than controls (N = 82, P = 0.048). This contrast is also visible in feto-maternal HLA-DRB1 compatibility, which was increased only among women with lcSSc (N = 33) compared with controls (N = 68, P = 0.003). Conclusion. For the first time, we showed that women with lcSSc and dcSSc hold male Mc in different blood compartments. Furthermore, a distinct pattern between the two SSc subtypes is observed for feto-maternal HLA-DRB1 compatibility. These results suggest a different mechanism behind each type of disease.</abstract><cop>Oxford</cop><pub>Oxford University Press</pub><pmid>19208687</pmid><doi>10.1093/rheumatology/ken505</doi><tpages>4</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adolescent Adult Aged Biological and medical sciences Blood Case-Control Studies Child Chimerism Diffuse cutaneous scleroderma Diseases of the osteoarticular system Female Histocompatibility Histocompatibility Testing HLA-DR Antigens HLA-DRB1 Chains Humans Limited cutaneous scleroderma Male Medical sciences Microchimerism Middle Aged Mothers Peripheral blood mononuclear cells Pregnancy - genetics Pregnancy - immunology Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis Scleroderma, Diffuse - genetics Scleroderma, Limited - genetics Scleroderma, Systemic - genetics Scleroderma, Systemic - immunology Y-chromosome Young Adult |
title | Male microchimerism and HLA compatibility in French women with sclerodema: a different profile in limited and diffuse subset |
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