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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
Main Authors: 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.
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cited_by cdi_FETCH-LOGICAL-c482t-ccd6bad66a73ac45c93f1261108c8950a242bb1efbcd11076e033f5f4b089a593
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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&amp;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. 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Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. 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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.</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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source Oxford Journals Online; Alma/SFX Local Collection
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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