Clinical significance of the fetal microchimerism for mother

Capa
  • Autores: Rumyantsev AG1, Kurcer MA2, Mareeva J.M3, Misjurin AV3, Roumiantsev SA4, Ustjugov AJ.3
  • Afiliações:
    1. 1 D. Rogachev Federal Scientific and Clinical Center of Pediatric Hematology, Oncology and Immunologyof the Ministry of Health and Social Development of the Russia, Moscow2 N.I. Pirogov Russian National Research Medical University of the Ministry of Healthand Social Development of the Russia, Moscow
    2. N.I. Pirogov Russian National Research Medical University of the Ministry of Healthand Social Development of the Russia, Moscow
    3. D. Rogachev Federal Scientific and Clinical Center of Pediatric Hematology, Oncology and Immunologyof the Ministry of Health and Social Development of the Russia, Moscow
    4. D. Rogachev Federal Scientific and Clinical Center of Pediatric Hematology, Oncology and Immunologyof the Ministry of Health and Social Development of the Russia, Moscow2 N.I. Pirogov Russian National Research Medical University of the Ministry of Healthand Social Development of the Russia, Moscow
  • Edição: Volume 7, Nº 2 (2012)
  • Páginas: 103-111
  • Seção: Articles
  • ##submission.dateSubmitted##: 11.01.2023
  • ##submission.datePublished##: 15.06.2012
  • URL: https://genescells.ru/2313-1829/article/view/121647
  • DOI: https://doi.org/10.23868/gc121647
  • ID: 121647


Citar

Texto integral

Acesso aberto Acesso aberto
Acesso é fechado Acesso está concedido
Acesso é fechado Acesso é pago ou somente para assinantes

Resumo

Fetal cells enter into mother`s body during pregnancy
and remain there for many years. In female body accumulate
genetically foreign cells of all pregnancies, regardless of what
they have ended (a miscarriage, an abortion or a childbirth). It
is shown that fetal cells are found in various maternal tissues
and organs including blood, bone marrow, liver, lungs and skin.
The interaction nature of foreign cells entering the mothers
body in a natural way with her own cells and immune system
of mother can be extrapolated to the study of chimerism in
the iatrogenic effects on the body, such as hematopoietic
stem cell transplantation or blood transfusion. Natural fetomaternal
microchimerism has important effect on the immune
status of women contributing to development of autoimmune
conditions and tolerance to transplants. Understanding
the fact that fetal cells able to pass through the placental
and blood brain barrier, to migrate in various tissues
and to differentiate in multiple cell types can be used for
development of cell therapy. The studies of long-term effects
feto- maternal microchimerism can get more favorable and
unfavorable prognostic criteria for womens health, but also
able to fundamentally change the understanding of current
principles of clinical genetics.
This paper presents an overview of knowledge about
microchimerism appeared during pregnancy and current views
on the implications of this unique biological phenomenon.

Sobre autores

A Rumyantsev

1 D. Rogachev Federal Scientific and Clinical Center of Pediatric Hematology, Oncology and Immunologyof the Ministry of Health and Social Development of the Russia, Moscow2 N.I. Pirogov Russian National Research Medical University of the Ministry of Healthand Social Development of the Russia, Moscow

1 D. Rogachev Federal Scientific and Clinical Center of Pediatric Hematology, Oncology and Immunologyof the Ministry of Health and Social Development of the Russia, Moscow2 N.I. Pirogov Russian National Research Medical University of the Ministry of Healthand Social Development of the Russia, Moscow

M Kurcer

N.I. Pirogov Russian National Research Medical University of the Ministry of Healthand Social Development of the Russia, Moscow

N.I. Pirogov Russian National Research Medical University of the Ministry of Healthand Social Development of the Russia, Moscow

Ju Mareeva

D. Rogachev Federal Scientific and Clinical Center of Pediatric Hematology, Oncology and Immunologyof the Ministry of Health and Social Development of the Russia, Moscow

D. Rogachev Federal Scientific and Clinical Center of Pediatric Hematology, Oncology and Immunologyof the Ministry of Health and Social Development of the Russia, Moscow

A Misjurin

D. Rogachev Federal Scientific and Clinical Center of Pediatric Hematology, Oncology and Immunologyof the Ministry of Health and Social Development of the Russia, Moscow

D. Rogachev Federal Scientific and Clinical Center of Pediatric Hematology, Oncology and Immunologyof the Ministry of Health and Social Development of the Russia, Moscow

S Roumiantsev

D. Rogachev Federal Scientific and Clinical Center of Pediatric Hematology, Oncology and Immunologyof the Ministry of Health and Social Development of the Russia, Moscow2 N.I. Pirogov Russian National Research Medical University of the Ministry of Healthand Social Development of the Russia, Moscow

D. Rogachev Federal Scientific and Clinical Center of Pediatric Hematology, Oncology and Immunologyof the Ministry of Health and Social Development of the Russia, Moscow2 N.I. Pirogov Russian National Research Medical University of the Ministry of Healthand Social Development of the Russia, Moscow

A Ustjugov

D. Rogachev Federal Scientific and Clinical Center of Pediatric Hematology, Oncology and Immunologyof the Ministry of Health and Social Development of the Russia, Moscow

D. Rogachev Federal Scientific and Clinical Center of Pediatric Hematology, Oncology and Immunologyof the Ministry of Health and Social Development of the Russia, Moscow

Bibliografia

  1. Adams K.M., Nelson J.L. Microcbimеrism: An investigative frontier in autoimmunity and transplantation. JAMA 2004; 291: 1127-31.
  2. Reed W., Lee T.H., Norris P.J. et al. Transfusion-associated microchimerism; A new complication of blood transfusions in severely injured patients. Semin. Hematoil. 2007; 44: 24-31.
  3. Bianchi D.W., Shuber A.P., Demaria M.A. et al. Fetal cells in maternal blood: Determination of purity and yield by quantitative polymerase chain reaction. Am. J. Obstet. Gynecol. 1994; 171: 922-6.
  4. Iverson C.M., Bianchi D.W., Cann H.M. et al. Detection and isolation of fetal ceils from maternal blood using the flоurescenceactivated cell sorter (FACS). Prenat. Diagn. 1981; 1: 61-73.
  5. Shalcv S.A., Shalev E., Pras E. et al. Evidence for blood chimerism in dizygotic spontaneous twin pregnancy discordant for Down syndrome. Prenat. Diagn. 2006; 26: 782-4.
  6. Srivatsa B., Srivatsa A., Johnson K.L. et al. Maternal cell microchimerism in newborn tissues. J. Pediatr. 2003; 142: 31-5
  7. O'Donoghue K., Chan J., Kennea N. et al. Microchimerism in female bone marrow and bone decades alter fetal mesenchymal Stemcell trafficking in pregnancy. Lancet 2004; 364: 179-82.
  8. Lapairc O., Hokgreve W., Osterwijk J.C. et al. Georg schmorl on trophobbsts in the maternal circulation. Placenta 2007; 28: 1-5.
  9. Hawes C.S., Suskin H.A., Petropoulps A. et al. A morphologic study of trophoblast isolated from peripheral blood of pregnant women. Am. J. Obstet. Gynecol. 1994; 170: 1297-300.
  10. Ganshirt D., garritsen H., Miny P. et al. Fetal cells in maternal circulation throughout gestation. Lancer 1994; 343: 1038-9.
  11. Khosrotehrani K., Bianchi D.W. Multi-lineage potential of fetal cells in maternal tissue: A legacy in reverse. J. Cell Sci. 2005; 118: 1559-63.
  12. O'Donoghue K., Choolani M., Chan J. et al. Identification of fetal mesenchymal stem cells in maternal blood: Implications for noninvasive prenatal diagnosis. Mol. Hum. Reprod. 2003; 9: 497-502.
  13. Khosrotehrani K., Johnson K.L., Guegan S. et al. Natural history of fetal cell microchimerism during and following murine pregnancy. J. Reprod. Immunol. 2005; 66:1-12.
  14. Geogiades P., Ferguson A.C., Burton G.J. Comparative developmental anatomy of the murine and human definitive placentae. Placenta 2002; 2(3): 3-19.
  15. Carter A.M. Animal models of human placentation - A review. Placenta 2007. 28(Suppl A): S41-7.
  16. Moffett A., Loke C. Immunology of placcntation in eutherian mammals. Nat. Rev. Immunol. 2006: 6: 584-94.
  17. Dawe G.S., Tan X.W., Xiao C.H. Cell migration from baby to mother. Cell Adges. Migrab. 2007; 1: 19-27.
  18. Engelhardt B. Molecular mechanisms involved in T cell migration across the blood-brain barrier. J. Neural. Transm. 2006; 13(3): 477-85.
  19. Tan X.W., Liao H., Sun L. et al. Fetal microchimerism in the maternal mouse brain: A novel population of fetal progenitor or stem cells able to cross the blood-brain barrier? Stem Cells 2005; 23: 1443-52.
  20. Vernochct C., Caucheteux S.M., Kanellopoulos-Langevuin C. Bi-directional cell trafficking between mother and fetus in mouse placenta. Placenta 2007. 28(7): 639-49. 23. Pertl B., Bianchi O.W. First trimester
  21. Pertl B., Bianchi O.W. First trimester prenatal diagnosis: Fetal cells in the maternal circulation Semin. Perinatol. 1999: 23: 393-402.
  22. Guetta E., Gordon D., Simchen M.J. et al. Hematopoietic progenitor cells as targets for non-invasive prenatal diagnosis: Detection of fetal CD34+ cells and assessment of post-delivery persistence in the maternal circulation. Blood Cells Mol. Dis. 2003; 30: 13-21.
  23. Van Z., Lambert N.C., Guthrie K.A. et al. Male microchimerism in women without sons: Quantitative assessment and correlation with pregnancy history. Am. J. Med. 2005; 118: 899-906.
  24. Guettier C., Sebagh M., Buard J. et al. Male cell microchimerism in normal and diseased female livers from fetal life to adulthood. Hepatology 2005; 42: 35-43.
  25. Landy H.J., Keith L.G. The vanishing twin: A review. Hum. Repeod. Update 1998; 4: 177-83.
  26. Veenstra A.l., Heieman M.J., Faas M.M. The immunology of successful pregnancy. Hum. Reprod. Update 2003; 9: 347-57.
  27. Carlson M.J., Doose J.M., Melchior B. et al. CNS immune privilege: Hiding in plain sight. Immunol. Rev. 2006; 213: 48-65.
  28. Bainbridge D.R. Evolution of mammalian pregnancy in the presence of the maternal immune system. Rev. Reprod. 2000; 5: 67-74.
  29. Khosrotehrani K., Jonson K.L., Lau J. et al. The influence of loss on the presence of fetal cell microchimerism: A systematic review. Arthritis Rheum. 2003; 48: 3237-41.
  30. Nelson J.L. Microchimerism in human and disease. Autoimmunity 2003; 36:5-9.
  31. Johnson K.L., Sarnura O., Nelson J.L. et al. Significant fetal cell microchimerism in a nontransfused woman with hepatitis C: Evidence of long-term survival and expansion. Hepatology 2002; 36: 1295-7.
  32. Cha D., Khosrotchrani K., Kim Y. et al. Cervical cancer and microchimerism. Obstct. Gynecol. 2003; 102: 774-81.
  33. Khosrotchrani K., Johnson K.L., Cha D.H. et al. Transfer of fetal cells with multilineage potential to maternal tissue. JAMA 2004; 292: 75-80.
  34. Mosca M., Curcio M., Lapi S. et al. Correlations or Y chromosome microchimerism with disease activity in patients with SLE: Analysis of preliminary data. Ann. Rheum. Dis. 2003; 62: 651-4.

Arquivos suplementares

Arquivos suplementares
Ação
1. JATS XML

Declaração de direitos autorais © Eco-Vector, 2012



СМИ зарегистрировано Федеральной службой по надзору в сфере связи, информационных технологий и массовых коммуникаций (Роскомнадзор).
Регистрационный номер и дата принятия решения о регистрации СМИ: 

Este site utiliza cookies

Ao continuar usando nosso site, você concorda com o procedimento de cookies que mantêm o site funcionando normalmente.

Informação sobre cookies