Literature DB >> 15550532

Male microchimerism in women with systemic sclerosis and healthy women who have never given birth to a son.

N C Lambert1, J M Pang, Z Yan, T D Erickson, A M Stevens, D E Furst, J L Nelson.   

Abstract

BACKGROUND: Male DNA or cells are often used to measure microchimerism in a woman. In studies of autoimmune diseases male microchimerism is most often attributed to the previous birth of a son.
OBJECTIVE: To determine the frequency of male microchimerism in healthy women or women with systemic sclerosis who had never given birth to a son.
METHODS: Real time quantitative polymerase chain reaction targeting the Y chromosome specific sequence DYS14 was employed to test DNA extracted from peripheral blood mononuclear cells of 26 women with systemic sclerosis and 23 healthy women who had never given birth to a son.
RESULTS: are expressed as the genome equivalent number of male cells per million host cells (gEq/mil).
Results: Male DNA was found in 15% of women with systemic sclerosis (range 0 to 23.7 gEq/mil) and in 13% of healthy women (range 0 to 5.1 gEq/mil). Although two women with male DNA had an induced abortion, most had no history of spontaneous or induced abortion (either systemic sclerosis or healthy).
CONCLUSIONS: Microchimerism with male DNA can be found in the circulation of women who have never given birth to a son. Thus sources other than a male birth must be considered when male DNA is used to measure microchimerism. Although other studies are needed, there was no apparent difference in women with systemic sclerosis and healthy women. Possible sources of male DNA include unrecognised male pregnancy or unrecognised male twin, an older male sibling with transfer through the maternal circulation, or sexual intercourse alone.

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Year:  2004        PMID: 15550532      PMCID: PMC1755528          DOI: 10.1136/ard.2004.029314

Source DB:  PubMed          Journal:  Ann Rheum Dis        ISSN: 0003-4967            Impact factor:   19.103


  14 in total

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2.  Scleroderma (systemic sclerosis): classification, subsets and pathogenesis.

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3.  Microchimerism of maternal origin persists into adult life.

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9.  Quantification of maternal microchimerism by HLA-specific real-time polymerase chain reaction: studies of healthy women and women with scleroderma.

Authors:  Nathalie C Lambert; Timothy D Erickson; Zhen Yan; Jennifer M Pang; Katherine A Guthrie; Daniel E Furst; J Lee Nelson
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Review 10.  The influence of fetal loss on the presence of fetal cell microchimerism: a systematic review.

Authors:  Kiarash Khosrotehrani; Kirby L Johnson; Joseph Lau; Alain Dupuy; Dong Hyun Cha; Diana W Bianchi
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Review 3.  Naturally acquired microchimerism: implications for transplantation outcome and novel methodologies for detection.

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Review 4.  Transfusion-associated microchimerism: the hybrid within.

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8.  Microchimerism of male origin in a cohort of Danish girls.

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Review 9.  Naturally acquired microchimerism.

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Review 10.  Why are women predisposed to autoimmune rheumatic diseases?

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