Free Fetal DNA in Maternal Circulation

JAMA ◽  
2004 ◽  
Vol 292 (23) ◽  
pp. 2835 ◽  
2019 ◽  
Vol 97 (Supplement_3) ◽  
pp. 256-257
Author(s):  
Hannah M Teague ◽  
Erika S Niland ◽  
Natalie L Pierce ◽  
J Bret Taylor ◽  
J Alison Brown

Abstract The presence of a male co-twin during pregnancy has been found to impact lifetime reproductive performance in the sibling ewe. XY chimerism, thought to originate from a male co-twin, has been observed in ewes, and may be associated with the rare development of freemartins. Fetal ram DNA has been observed in the maternal circulation during pregnancy, but it is unknown if this chimerism persists after parturition. The objective of this study was to determine if fetal male cells were present in soft tissues of older ewes and if so, does the occurrence differ with lifetime offspring sex ratio. Eight ewes approximately 7-years-old and having given birth to at least 71% female (n = 4) or 82% males (n = 4) were tested. DNA was extracted from 10 different tissues from each ewe (n = 80). In triplicate, real-time PCR (qPCR) was used to identify the presence of the SRY gene in each sample. Using the SRY primer pair, male DNA was identified in the brain (between 1.25 ng / µL and 125 pg / µL) and liver (between 125 and 12.5 pg / µL) from a ewe that had given birth to two males during her lifetime. If any additional male fetal DNA was present, it was below the detectable limits. In addition to giving birth to two males, this ewe was also born with two male co-siblings, thus the origin (sibling or offspring) of the male DNA is not known. These data suggest fetal cell transfer in sheep is possible and the frequency of fetal microchimerism is not associated with sex ratio of lifetime offspring.


Author(s):  
Sashi C. Siva ◽  
Sylvia I. Johnson ◽  
Sharon A. Mccracken ◽  
Jonathan M. Morris

2008 ◽  
Vol 28 (4) ◽  
pp. 304-308 ◽  
Author(s):  
L. Hui ◽  
J. I. Vaughan ◽  
M. Nelson

2015 ◽  
Vol 212 (1) ◽  
pp. S65-S66
Author(s):  
Edward Wolf ◽  
Victoria DeSantos ◽  
Christopher McNamara ◽  
Natalie Porat ◽  
Richard Miller ◽  
...  

2015 ◽  
Vol 3 (6) ◽  
pp. 489-491 ◽  
Author(s):  
Ron Hochstenbach ◽  
Peter G. J. Nikkels ◽  
Martin G. Elferink ◽  
Martijn A. Oudijk ◽  
Carla Oppen ◽  
...  

2019 ◽  
Vol 23 (3) ◽  
pp. 156-167
Author(s):  
sara mahmoud ◽  
hasnaa aboalwafa ◽  
Eman Ali ◽  
Nesma Ahmed ◽  
mohamed mahmoud ◽  
...  

2021 ◽  
Vol 9 (4) ◽  
pp. 170-176
Author(s):  
Rafal Sibiak ◽  
Ewa Wender-Ożegowska

Abstract Trophoblast cells can be detected and isolated from the cervical epithelial cells obtained via various techniques of trans-cervical samples collection such as a mucus aspiration, endocervical lavage, or standard cervical brushing in the early first trimester, even from the 5 weeks’ gestation. Isolated fetal cells can be used in the early prediction of fetal sex, prenatal diagnostics of the most common aneuploidies, and any other genetic abnormalities. Nevertheless, the collection of trophoblastic cells has limited efficacy compared to currently used methods of detection of free fetal DNA in maternal circulation or other protocols of invasive prenatal diagnostics available at later stages of pregnancy. In the past years, trans-cervical cell samples were collected mainly in women before planned pregnancy termination. The early trophoblastic cells isolation from women in ongoing pregnancies opens new perspectives for further studies focused on the elucidation of pathophysiology of numerous pregnancy-related complications.


Sign in / Sign up

Export Citation Format

Share Document