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Microchimerism in female bone marrow and bone decades after fetal mesenchymal stem-cell trafficking in pregnancy

  • Keelin O'Donoghue
  • , Jerry Chan
  • , Josu De La Fuente
  • , Nigel Kennea
  • , Ann Sandison
  • , Jonathan R. Anderson
  • , Irene A.G. Roberts
  • , Nicholas M. Fisk
  • Imperial College London
  • University College London
  • Imperial College Healthcare NHS Trust

Research output: Contribution to journalArticlepeer-review

Abstract

Fetal cells enter maternal blood during pregnancy and persist in women with autoimmune disease. The frequency of subsequent fetomaternal microchimerism in healthy women and its cell type is unknown. To test the hypothesis that fetal mesenchymal stem cells persist in maternal organs, we studied female bone marrow and ribs. Male cells were identified by XY fluorescence in-situ hybridisation in marrow-derived mesenchymal stem cells and in rib sections from all women with male pregnancies, but not in controls (9/9 vs 0/5, p=0·0005). We conclude that fetal stem cells transferred into maternal blood engraft in marrow, where they remain throughout life. This finding has implications for normal pregnancy, for obstetric complications that increase fetomaternal trafficking, and for graft survival after transplantation.

Original languageEnglish
Pages (from-to)179-182
Number of pages4
JournalThe Lancet
Volume364
Issue number9429
DOIs
Publication statusPublished - 10 Jul 2004
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

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