Literature DB >> 18539707

Pregnancy, chimerism and lupus nephritis: a multi-centre study.

I C L Kremer Hovinga1, M Koopmans, C Grootscholten, A M van der Wal, M Bijl, R H W M Derksen, A E Voskuyl, E de Heer, J A Bruijn, J H M Berden, I M Bajema.   

Abstract

Chimerism occurs twice as often in the kidneys of women with lupus nephritis as in normal kidneys and may be involved in the pathogenesis of systemic lupus erythematosus. Pregnancy is considered the most important source of chimerism, but the exact relationship between pregnancy, the persistence of chimeric cells and the development of systemic lupus erythematosus has not been investigated. Renal biopsies and clinical data from patients in the First Dutch Lupus Nephritis Study were used. Chimeric cells were identified by in-situ hybridization of the Y chromosome. A questionnaire was used to obtain detailed reproductive data including pregnancy history and miscarriages. Chimerism was found in 12 of 26 (46%) renal biopsies. Of the 12 chimeric women, 5 reported a pregnancy; of 14 women who were not chimeric, 8 reported a pregnancy. Chimeric women who had been pregnant reported significantly more pregnancies than non-chimeric women who had been pregnant (P=0.04). The median age of the youngest child was higher in chimeric women (19 years) than in non-chimeric women (6 years). Despite the attention given to pregnancy histories with respect to chimerism, this study shows that in patients with systemic lupus erythematosus, a clear-cut relationship is not apparent. A considerable number of chimeric women did not report a pregnancy: in these women, other sources of chimerism must be considered. Our data support the theory that only certain subsets of chimeric cells persist into the maternal circulation after pregnancy.

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Year:  2008        PMID: 18539707     DOI: 10.1177/0961203308089324

Source DB:  PubMed          Journal:  Lupus        ISSN: 0961-2033            Impact factor:   2.911


  4 in total

Review 1.  The unexplained female predominance of systemic lupus erythematosus: clues from genetic and cytokine studies.

Authors:  Corinna E Weckerle; Timothy B Niewold
Journal:  Clin Rev Allergy Immunol       Date:  2011-02       Impact factor: 8.667

2.  Variables associated to fetal microchimerism in systemic lupus erythematosus patients.

Authors:  Greiciane Maria da Silva Florim; Heloisa Cristina Caldas; Erika Cristina Pavarino; Eny Maria Goloni Bertollo; Ida Maria Maximina Fernandes; Mario Abbud-Filho
Journal:  Clin Rheumatol       Date:  2015-11-25       Impact factor: 2.980

3.  Male microchimerism at high levels in peripheral blood mononuclear cells from women with end stage renal disease before kidney transplantation.

Authors:  Laetitia Albano; Justyna M Rak; Doua F Azzouz; Elisabeth Cassuto-Viguier; Jean Gugenheim; Nathalie C Lambert
Journal:  PLoS One       Date:  2012-03-05       Impact factor: 3.240

4.  Fetal microchimerism in kidney biopsies of lupus nephritis patients may be associated with a beneficial effect.

Authors:  Greiciane M S Florim; Heloisa C Caldas; Julio C R de Melo; Maria Alice S F Baptista; Ida M M Fernandes; Marcela Savoldi-Barbosa; Gustavo H Goldman; Mario Abbud-Filho
Journal:  Arthritis Res Ther       Date:  2015-04-15       Impact factor: 5.156

  4 in total

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