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Detection of fetal cells present in transcervical samples

Published online by Cambridge University Press:  15 January 2010

Matteo Adinolfi*
Affiliation:
Department of Obstetrics and Gynaecology and Galton Laboratory, University College London, London.
*
Professor Matteo Adinolfi, The Galton Laboratory, Department of Genetics and Biometry, University College London, Wolfson House, 4 Stephenson Way, London NW1 2HE.

Extract

In 1971 Shettles postulated that, during pregnancy, chorionic cellular elements from degenerating villi were shed into the endocervical canal and could be analysed to assess fetal sex. Accordingly, he retrieved transcervical cells (TCC's) with cotton swabs and tested them for the presence of the Y chromosome using a fluorescent dye (quinacrine mustard). At the time of publishing his note, he had correctly diagnosed the sex of 10 fetuses in 18 pregnancies investigated.

Type
Research Article
Copyright
Copyright © Cambridge University Press 1996

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References

1Shettles, LB. Use of the Y chromosome in prenatal sex determination. Nature 1971; 230: 52.CrossRefGoogle Scholar
2Warren, R, Sanchez, L, Hammond, D, McLeod, A. Prenatal sex determination from exfoliated cells found in cervical mucus Am J Hum Genet 1972; 24: 22.Google Scholar
3Varner, RE. Fluorescent Y bodies from endocervical smears for prenatal sex detection Ala J Med Sci 1977; 14, 438.Google ScholarPubMed
4Bobrów, M, Lewis, BV. Unreliability of fetal sexing using cervical material Lancet 1971; 2: 486.CrossRefGoogle ScholarPubMed
5Tsuji, K, Sasaki, M. Absence of Y-body in the cervical mucus of pregnant women Nature 1973; 243: 539.CrossRefGoogle ScholarPubMed
6Goldstein, AI, Lukesh, RC, Ketchum, M. Prenatal sex determination by fluorescent staining of the cervical smear for the presence of a Y chromosome: an evaluation. Am J Obstet Gynecol 1973; 115: 866.CrossRefGoogle Scholar
7Manuel, M, Park, IJ, Jones, HW. Prenatal sex determination by fluorescent staining of cells for the presence of Y chromatin. Am J Obstet Gynecol 1974; 119: 853–54CrossRefGoogle ScholarPubMed
8Amankwah, KS, Bond, EC. Unreliability of prenatal determination of fetal sex with the use of Y-body fluorescence in midcervical smears. Am J Obstet Gynecol 1978; 130: 300301Google ScholarPubMed
9Rhine, SA, Cain, JL, Cleary, RL, Palmer, CG, Thompson, JF. Prenatal sex detection with endocervical smears: successful results utilizing Y-body fluorescence. Am J Obstet Gynecol 1975; 122: 155160CrossRefGoogle Scholar
10Rhine, SA, Palmer, CG, Thompson, JF. A simple alternative to amniocentesis for first trimester prenatal diagnosis. Birth Defects 1977; 12: 231–47Google Scholar
11Rhine, SA, Milunsky, A. Utilization of trophoblast for early prenatal diagnosis. In: Milunsky, A ed. Genetic disorders and the fetus New York; Plenum Press, 1979: 527539.CrossRefGoogle Scholar
12Goldberg, M, Chen, ATL, Ahn, YW, Reidy, JA, First-trimester fetal chromosomal diagnosis using endocervical lavage: a negative evaluation. Am J Obstet Gynecol 1980; 138: 436440.CrossRefGoogle ScholarPubMed
13Griffith-Jones, MD, Miller, D, Lilford, RJ, Scott, J, Bulmer, J. Detection of fetal DNA in transcervical swabs from the first trimester of pregnancies by gene amplification: a new route to prenatal diagnosis? Br J Obstet Gynaecol 1992; 99: 508–11CrossRefGoogle ScholarPubMed
14Morris, N, Williamson, R. Non-invasive first trimester antenatal diagnosis. Br J Obstet Gynaecol 1992; 99: 446–48CrossRefGoogle ScholarPubMed
15Adinolfi, M, Da vies, A, Sharif, S, Soothill, P, Rodeck, C. Detection of trisomy 18 and Y-derived sequences in fetal nucleated cells obtained by transcervical flushing. Lancet 1993; 342: 403404CrossRefGoogle ScholarPubMed
16Adinolfi, M, Soothill, P, Rodeck, C. A simple alternative to amniocentesis? Prenat Diagn 1994; 14: 231–32CrossRefGoogle ScholarPubMed
17Adinolfi, M. Non- or minimally invasive prenatal diagnostic tests on maternal blood samples or transcervical cells. Prenat Diag 1995; 15: 889–97CrossRefGoogle ScholarPubMed
18Rodeck, C, Tutschek, B, Sherlock, J, Kingdom, J. Methods for the collection of transcervical samples during the first trimester of gestation. Prenat Diagn 1995; 15: 933–43CrossRefGoogle Scholar
19Adinolfi, M, Sherlock, J, Tutschek, B, Haider, A, Delhanty, J, Rodeck, C. Detection of fetal cells in transcervical samples and prenatal diagnosis of chromosomal abnormalities. Prenat Diagn 1995; 15: 943–51CrossRefGoogle ScholarPubMed
20Kingdom, J, Sherlock, J, Rodeck, C, Adinolfi, M. Detection of trophoblast cells in transcervical samples collected by lavage or cytobrush. Obstet Gynecol 1995; 86: 283–88.CrossRefGoogle ScholarPubMed
21Bulmer, JN, Rodeck, C, Adinolfi, M. Immunohistochemical characterisation of cells retrieved by transcervical sampling in early pregnancy. Prenat Diag in press.Google Scholar
22Briggs, J, Miller, D, Bulmer, J, Griffith-Jones, M, Rame, V, Lilford, R. Non-syncytial sources of fetal DNA in transcervically recovered cell populations. Mol Hum Repród 1995; 10: 749–55.CrossRefGoogle ScholarPubMed
23Adinolfi, M, Sherlock, J, Soothill, P, Rodeck, C. Molecular evidence of fetal-derived chromosome 21 markers (STRs) in transcervical samples. Prenat Diagn 1995; 15: 3539.CrossRefGoogle ScholarPubMed
24Mansfield, ES. Diagnosis of Down Syndrome and other aneuploidies using quantitative polymerase chain reaction and small tandem repeat polymorphisms. Hum Mol Genet 1993; 2: 4350CrossRefGoogle ScholarPubMed
25Pertl, B, Yau, SC, Sherlock, J, Davies, AF, Mathew, CG, Adinolfi, M. Rapid molecular method for prenatal detection of Down syndrome. Lancet 1994; 343: 1197–98CrossRefGoogle Scholar
26Adinolfi, MC, Sherlock, J, Pertl, B. Rapid detection of selected aneuploidies by quantitative fluorescent PCR. Bioessays 1995; 17: 661–64CrossRefGoogle ScholarPubMed
27Ishai, D, Amiel, A, Duikman, R, Cogan, O, Lichtenstein, Z, Abramovici, H, Fejgin, MD. Uterine cavity lavage: adding FISH to conventional cytogenetics for embryonic sexing and diagnosing common chromosomal aberrations. Prenat Diagn 1995; 15: 961–67CrossRefGoogle Scholar
28Tutschek, B, Sherlock, J, Haider, A, Delhanty, J, Rodeck, C, Adinolfi, M. Isolation of fetal cells from transcervical samples by micromanipulation: diagnosis of fetal aneuploidy and molecular confirmation of fetal origin. Prenat Diagn 1995; 15: 951–61CrossRefGoogle ScholarPubMed
29Adinolfi, M, Sherlock, J, Kemp, T, Carri«, T, Soothill, P, Kingdom, et al. Prenatal detection of fetal RhD DNA sequences in transcervical samples. Lancet 1995; 345: 318–19CrossRefGoogle ScholarPubMed
30Adinolfi, M. Breaking the blood barrier. Nature Genet 1992; 1(5): 316–18.CrossRefGoogle ScholarPubMed