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Current knowledge about fetal blood cells in the maternal circulation
1Department of Pediatrics, New England Medical Center, Boston, MA 02111, USA. Diana.Bianchi@es.nemc.org
Journal of Perinatal Medicine
|October 17, 1998
Summary
Noninvasive prenatal genetic analysis using fetal cells from maternal blood is advancing. This method offers expanded diagnostic possibilities for fetal aneuploidy and genetic testing during pregnancy.
Area of Science:
- Reproductive biology
- Genetics
- Cellular biology
Background:
- Fetal cells are present in maternal circulation.
- Isolation methods vary in cost and expertise.
- Specific fetal cell types like trophoblasts and nucleated erythrocytes are targeted.
Purpose of the Study:
- To review the current status and future of noninvasive prenatal genetic analysis.
- To discuss the isolation and identification of fetal cells from maternal blood.
- To explore diagnostic applications and implications of fetal cells in maternal circulation.
Main Methods:
- Isolation of fetal cells from maternal blood using various separation techniques.
- Identification of fetal cells based on cell surface and cytoplasmic protein expression.
- Screening for aneuploidy via chromosome-specific probes on interphase nuclei.
- Single gene and single cell analysis for expanded diagnostics.
Main Results:
- Improved fetal cell identification through protein expression understanding.
- Detection of aneuploidy in isolated fetal cells.
- Fetal cells are more common in trisomy 21 pregnancies.
- Fetomaternal transfusion at delivery can lead to fetal cell microchimerism.
Conclusions:
- Noninvasive prenatal genetic analysis via fetal cell isolation is a progressing field.
- Technical challenges remain, but diagnostic potential is significant.
- Fetal cells in maternal blood offer insights into pregnancy immunobiology and potential maternal disease links.