HLA-G positive trophoblastic cells in transcervical samples and their isolation and analysis by laser microdissection and QF-PCR.

Abstract:

OBJECTIVE:To assess the frequency of cytotrophoblastic cells in endocervical samples collected by lavage at early stages of gestation using a specific anti-HLA-G McAb (G233). From a set of four selected samples, cells identified by immunostaining were collected by laser microdissection and then tested by quantitative fluorescent polymerase chain reaction (QF-PCR) for the presence of paternally derived DNA markers, in order to establish their fetal origin. METHODS:Syncytial fragments and cytotrophoblastic cells from 23 transcervical samples were identified by immunostaining with McAb G233 reacting against HLA-G antigen and with antibodies against cytokeratin. Slides from the same samples were also tested by fluorescent in situ hybridization (FISH), while selected samples were analysed by QF-PCR. Slides from four samples retrieved from mothers with male fetuses were immunolabelled and then cytotrophoblastic cells, syncytial fragments and maternal epithelial cells were collected by laser microdissection and tested by QF-PCR. RESULTS:All endocervical samples retrieved from mothers with male fetuses were found to contain some cells with chromosome Y-specific signals when tested by FISH. Using McAb anti- HLA-G, cytotrophoblastic cellular elements were detected in about 50% of the samples. From four samples, cellular elements identified by immunostaining as cytotrophoblast or syncytial fragments were collected by laser microdissection and shown to be of fetal origin when tested by QF-PCR for the presence of fetal DNA markers. CONCLUSIONS:These results confirm that, during an early phase of gestation, fetal cells are released in the lower uterine cavity and that they can be isolated and analysed for prenatal diagnosis of single gene defects and aneuploidies.

journal_name

Prenat Diagn

journal_title

Prenatal diagnosis

authors

Bulmer JN,Cioni R,Bussani C,Cirigliano V,Sole F,Costa C,Garcia P,Adinolfi M

doi

10.1002/pd.511

subject

Has Abstract

pub_date

2003-01-01 00:00:00

pages

34-9

issue

1

eissn

0197-3851

issn

1097-0223

journal_volume

23

pub_type

杂志文章
  • Prenatal exclusion of Stickler syndrome.

    abstract::Stickler syndrome is an autosomal dominant disorder of the connective tissue which includes ocular and systemic manifestations. We report on a large kindred in which we were able to demonstrate very tight linkage between the disease and the type II collagen gene (COL2A1) (LOD score 3.91 at theta = 0). In a family in w...

    journal_title:Prenatal diagnosis

    pub_type: 杂志文章

    doi:10.1002/pd.1970140211

    authors: Zlotogora J,Granat M,Knowlton RG

    更新日期:1994-02-01 00:00:00

  • Three-dimensional ultrasound in prenatal diagnosis of skeletal dysplasia.

    abstract::A lethal form of bone dysplasia, platylospondylic lethal chondrodysplasia, was diagnosed prenatally using three-dimensional ultrasound. The various types of three-dimensional imaging mode provided diagnostic details not available by conventional two-dimensional ultrasound. The diagnosis was made after referral in the ...

    journal_title:Prenatal diagnosis

    pub_type: 杂志文章

    doi:10.1002/pd.1970150413

    authors: Steiner H,Spitzer D,Weiss-Wichert PH,Graf AH,Staudach A

    更新日期:1995-04-01 00:00:00

  • Carrier detection of Duchenne muscular dystrophy through analysis of DNA from deciduous teeth of a dead affected child.

    abstract::The sister of a child affected by Duchenne muscular dystrophy (DMD) was referred for genetic counselling to assess the risk of her being a carrier. Her brother had died 15 years previously at the age of 8. There were no other affected males in the family. There were no methods for DNA investigation at the time of the ...

    journal_title:Prenatal diagnosis

    pub_type: 杂志文章

    doi:10.1002/pd.1970150715

    authors: Restagno G,Ferrone M,Doriguzzi C,Palmucci L,Mongini T,Carbonara A

    更新日期:1995-07-01 00:00:00

  • Risk of congenital heart diseases associated with NAT2 genetic polymorphisms and maternal polycyclic aromatic hydrocarbons exposure.

    abstract:OBJECTIVE:N-Acetyltransferase 2 (NAT2) is a phase II xenobiotic-metabolizing enzyme participating in the detoxification of toxic arylamines and aromatic amines. The present study was designed to investigate whether maternal NAT2 genetic polymorphisms are associated with fetal susceptibility to congenital heart diseases...

    journal_title:Prenatal diagnosis

    pub_type: 杂志文章

    doi:10.1002/pd.5516

    authors: Tao J,Li N,Liu Z,Qiu J,Deng Y,Li X,Chen M,Yu J,Zhu J,Yu P,Wang Y

    更新日期:2019-10-01 00:00:00

  • Early vaginal bleeding and first-trimester markers for Down syndrome.

    abstract:OBJECTIVES:To assess the effect of early vaginal bleeding on first-trimester markers for Down syndrome. METHODS:A retrospective study was conducted on 2330 normal singleton fetuses who underwent first-trimester combined screening for Down syndrome based on ultrasound and maternal serum markers. Fetal nuchal translucen...

    journal_title:Prenatal diagnosis

    pub_type: 杂志文章

    doi:10.1002/pd.611

    authors: De Biasio P,Canini S,Crovo A,Prefumo F,Venturini PL

    更新日期:2003-06-01 00:00:00

  • Prenatal echocardiographic diagnosis of right atrial isomerism.

    abstract::A prenatal diagnosis of right atrial isomerism is often inferred through the recognition of a constellation of cardiac anomalies on the four-chamber view or by the detection of visceral heterotaxy and asplenia. However, the actual occurrence of discordance between the arrangement of the atria and thoracic and abdomina...

    journal_title:Prenatal diagnosis

    pub_type: 杂志文章

    doi:10.1002/pd.1970140410

    authors: Colloridi V,Pizzuto F,Ventriglia F,Giancotti A,Pachì A,Gallo P

    更新日期:1994-04-01 00:00:00

  • Recurrent congenital toxoplasmosis in a woman with lupus erythematosus.

    abstract::We describe the case of a patient with systemic lupus erythematosus, treated by corticosteroids, who presented during two successive pregnancies with serological reactivation of toxoplasmosis associated with fetal lesions. The first infected fetus died in utero with signs of hydrops. The second fetus was treated in ut...

    journal_title:Prenatal diagnosis

    pub_type: 杂志文章

    doi:10.1002/pd.1970151216

    authors: D'Ercole C,Boubli L,Franck J,Casta M,Harle JR,Chagnon C,Cravello L,Leclaire M,Blanc B

    更新日期:1995-12-01 00:00:00

  • Preimplantation genetic diagnosis for familial amyloidotic polyneuropathy (FAP).

    abstract::Preimplantation genetic diagnosis (PGD) was developed more than a decade ago to offer an alternative to prenatal diagnosis for couples at risk of transmitting an inherited disease to their offspring. Portuguese-type familial amyloidotic polyneuropathy (FAP type I), is an autosomal dominant disease presenting an inheri...

    journal_title:Prenatal diagnosis

    pub_type: 杂志文章

    doi:10.1002/pd.250

    authors: Carvalho F,Sousa M,Fernandes S,Silva J,Saraiva MJ,Barros A

    更新日期:2001-12-01 00:00:00

  • Cervical teratoma: prenatal diagnosis and long-term follow-up.

    abstract::Cervical teratomas are rare tumours which are the result of abnormal prenatal development. They are usually detected at birth, but can occasionally remain silent until adulthood. Obstruction of the airway is the major challenge in the neonatal period. Prenatal diagnosis allows for early consultation with paediatric su...

    journal_title:Prenatal diagnosis

    pub_type: 杂志文章

    doi:

    authors: Kerner B,Flaum E,Mathews H,Carlson DE,Pepkowitz SH,Hixon H,Graham JM Jr

    更新日期:1998-01-01 00:00:00

  • Prenatal diagnosis of a mosaic extra structurally abnormal chromosome by spectral karyotyping.

    abstract::A de novo mosaic extra structurally abnormal chromosome (ESAC) was detected in 33 per cent of cultured amniotic fluid cells from a pregnant woman. Neither Q-banding nor fluorescence in situ hybridization (FISH) employing a DNA probe for nucleolar organizer region demonstrated the presence of satellites on the ESAC. Sp...

    journal_title:Prenatal diagnosis

    pub_type: 杂志文章

    doi:

    authors: Ning Y,Laundon CH,Schröck E,Buchanan P,Ried T

    更新日期:1999-05-01 00:00:00

  • Quantification of human amniotic fluid constituents by high resolution proton nuclear magnetic resonance (NMR) spectroscopy.

    abstract::We have investigated the ability of high-resolution proton NMR spectroscopy to provide a biochemical constituent screening of human amniotic fluid (AF). Proton NMR spectra were obtained at 300 MHz on AF from patients undergoing amniocentesis in the mid-trimester. Only AF from normal pregnancies (normal fetal karyotype...

    journal_title:Prenatal diagnosis

    pub_type: 杂志文章

    doi:10.1002/pd.1970130609

    authors: Sims CJ,Fujito DT,Burholt DR,Dadok J,Giles HR,Wilkinson DA

    更新日期:1993-06-01 00:00:00

  • Maternal serum screening for down syndrome in pregnancies conceived by intra-uterine insemination.

    abstract::The purpose of our study was to assess the influence of intra-uterine insemination (IUI) on the results of maternal serum Down syndrome screening. 43 women with IUI pregnancies and 4507 healthy women who conceived were studied. Ovulation in IUI pregnancies was induced by clomiphene and/or human menopausal gonadotrophi...

    journal_title:Prenatal diagnosis

    pub_type: 杂志文章

    doi:10.1002/(sici)1097-0223(199911)19:11<1012::aid-pd6

    authors: Hsu TY,Ou CY,Hsu JJ,Kung FT,Chang SY,Soong YK

    更新日期:1999-11-01 00:00:00

  • The thick heterogeneous (jellylike) placenta: a strong predictor of adverse pregnancy outcome.

    abstract:OBJECTIVE:To present a series of cases with a sonographic thick and heterogeneous placenta, and to review the literature. METHODS:A series of 16 cases were analyzed. A heterogeneous placenta was defined as a thick placenta with a patchy decrease of echogenicity, which quivered like jelly to sharp abdominal pressure. A...

    journal_title:Prenatal diagnosis

    pub_type: 杂志文章,评审

    doi:10.1002/pd.828

    authors: Raio L,Ghezzi F,Cromi A,Nelle M,Dürig P,Schneider H

    更新日期:2004-03-01 00:00:00

  • First-trimester sonographic diagnosis of distal urethral atresia with megalourethra in VACTERL association.

    abstract::Congenital megalourethra is a rare disorder. We present an early case diagnosed in the first trimester. Prenatal ultrasound showed a megalourethra with a normal fetal bladder, hyperechogenic cystic right kidney and single umbilical artery. After termination of pregnancy, necropsy confirmed all sonographic findings and...

    journal_title:Prenatal diagnosis

    pub_type: 杂志文章

    doi:10.1002/pd.328

    authors: Krapp M,Geipel A,Germer U,Krokowski M,Gembruch U

    更新日期:2002-05-01 00:00:00

  • Clinical, cytogenetic, and molecular analyses of prenatally diagnosed mosaic tetrasomy for distal chromosome 15q and review of the literature.

    abstract:OBJECTIVES:To present prenatally detected mosaic tetrasomy for distal chromosome 15q and a review of the literature. CLINICAL SUBJECT AND METHODS:Amniocentesis was performed at 17 weeks' gestation because of advanced maternal age. Cytogenetic analysis revealed mosaicism for an analphoid supernumerary marker chromosome...

    journal_title:Prenatal diagnosis

    pub_type: 杂志文章,评审

    doi:10.1002/pd.977

    authors: Chen CP,Lin CC,Li YC,Chern SR,Lee CC,Chen WL,Lee MS,Wang W,Tzen CY

    更新日期:2004-10-01 00:00:00

  • Amiodarone treatment in pregnancy for dilatative cardiomyopathy with ventricular malignant extrasystole and normal maternal and neonatal outcome.

    abstract::Amiodarone treatment in pregnancy might be difficult to handle because of the long half-life of the drug (14-28 days up to 2 months) and because it reduces maternal and neonatal thyroid activity. Although short-term use in pregnancy has been described in cases of fetal supraventricular tachycardia, there are few repor...

    journal_title:Prenatal diagnosis

    pub_type: 杂志文章

    doi:10.1002/pd.1970120903

    authors: Valensise H,Civitella C,Garzetti GG,Romanini C

    更新日期:1992-09-01 00:00:00

  • Noninvasive prenatal detection of sex chromosomal aneuploidies by sequencing circulating cell-free DNA from maternal plasma.

    abstract:OBJECTIVE:Whole-genome sequencing of circulating cell free (ccf) DNA from maternal plasma has enabled noninvasive prenatal testing for common autosomal aneuploidies. The purpose of this study was to extend the detection to include common sex chromosome aneuploidies (SCAs): [47,XXX], [45,X], [47,XXY], and [47,XYY] syndr...

    journal_title:Prenatal diagnosis

    pub_type: 杂志文章

    doi:10.1002/pd.4127

    authors: Mazloom AR,Džakula Ž,Oeth P,Wang H,Jensen T,Tynan J,McCullough R,Saldivar JS,Ehrich M,van den Boom D,Bombard AT,Maeder M,McLennan G,Meschino W,Palomaki GE,Canick JA,Deciu C

    更新日期:2013-06-01 00:00:00

  • Evaluation of population parameters and mathematical strategies for the calculation of prenatal risk of Down syndrome in the first trimester of pregnancy.

    abstract:OBJECTIVE:To evaluate the population parameters applied to the calculation of risk for Down syndrome (DS) in the first trimester screening (FTS) and the comparison of performance obtained including or excluding maternal age from the mathematical algorithm. METHODS:Three different calculation engines for prenatal risk ...

    journal_title:Prenatal diagnosis

    pub_type: 杂志文章

    doi:10.1002/pd.2937

    authors: Martínez-Morillo E,García BP,Calvo FM,Alvarez FV

    更新日期:2012-03-01 00:00:00

  • SARS-CoV2 (COVID-19) infection: is fetal surgery in times of national disasters reasonable?

    abstract::Even though the global COVID-19 pandemic may affect how medical care is delivered in general, most countries try to maintain steady access for women to routine pregnancy care, including fetal anomaly screening. This means that, also during this pandemic, fetal anomalies will be detected, and that discussions regarding...

    journal_title:Prenatal diagnosis

    pub_type: 信件

    doi:10.1002/pd.5702

    authors: Deprest J,Van Ranst M,Lannoo L,Bredaki E,Ryan G,David A,Richter J,Van Mieghem T

    更新日期:2020-12-01 00:00:00

  • A normal 46,XX infant with a 46,XX/69,XXY placenta: a major contribution to the placenta is from a resorbed twin.

    abstract::A predominantly triploid 69,XXY placenta was found associated with a normal 46,XX infant. Therefore, a triploid placenta is apparently capable of supporting normal fetal development. The chromosome and pathological results support the conclusion that the triploid placenta originates from a 'vanishing twin' pregnancy. ...

    journal_title:Prenatal diagnosis

    pub_type: 杂志文章

    doi:10.1002/pd.1970110705

    authors: Callen DF,Fernandez H,Hull YJ,Svigos JM,Chambers HM,Sutherland GR

    更新日期:1991-07-01 00:00:00

  • Prenatal diagnosis of a homologous Robertsonian translocation involving chromosome 15.

    abstract::We report the prenatal diagnosis of a fetus with a de novo Robertsonian translocation: 45,XY,der(15;15)(q10;q10). Although Robertsonian translocations are common chromosomal rearrangements, those involving homologous chromosomes are infrequent. Since chromosome 15 is imprinted, uniparental disomy (UPD) is a concern wh...

    journal_title:Prenatal diagnosis

    pub_type: 杂志文章

    doi:10.1002/pd.133

    authors: Abrams DJ,Aronoff AR,Ann Berend S,Roa BB,Shaffer LG,Geier MR

    更新日期:2001-08-01 00:00:00

  • Maternal serum superoxide dismutase (SOD): a possible marker for screening Down syndrome affected pregnancies.

    abstract::Superoxide dismutase (SOD: EC1.15.1.1) has been shown to increase in Down syndrome (DS) subjects and in amniotic fluid from DS affected pregnancies. In order to verify a possible increase of maternal serum SOD in DS affected pregnancies and its possible contribution in prenatal screening, the serum enzyme activity was...

    journal_title:Prenatal diagnosis

    pub_type: 杂志文章

    doi:

    authors: Ognibene A,Ciuti R,Tozzi P,Messeri G

    更新日期:1999-11-01 00:00:00

  • Aneuploidy and cystic hygroma detectable by ultrasound.

    abstract::During one year, five second trimester fetuses with cystic hygromata and varying degrees of oedema presented to the authors from hospitals in the West of Scotland. Two fetuses had 45X karyotypes, one each had 47XY + 21 and 47XX + 18 karyotypes, and the fifth had a normal 46XY karyotype. Fetal oedema detectable by ultr...

    journal_title:Prenatal diagnosis

    pub_type: 杂志文章

    doi:10.1002/pd.1970040509

    authors: Redford DH,McNay MB,Ferguson-Smith ME,Jamieson ME

    更新日期:1984-09-01 00:00:00

  • Identification of expressed sequence tags preferentially expressed in human placentas by in silico subtraction.

    abstract:OBJECTIVES:To identify expressed sequence tag (EST) clusters preferentially expressed in placentas. METHODS:The National Center for Biotechnology's online UniGene database contains 14 placenta libraries. In silico (computer-based) subtraction compared placenta libraries against the remaining libraries to identify tran...

    journal_title:Prenatal diagnosis

    pub_type: 杂志文章

    doi:10.1002/pd.608

    authors: Miner D,Rajkovic A

    更新日期:2003-05-01 00:00:00

  • Fetal aqueductal stenosis: Prenatal diagnosis and intervention.

    abstract::Fetal severe central nervous system ventriculomegaly is associated with poor neurologic outcomes, usually driven by a primary malformation, deformation, or disruption of brain parenchyma. In utero shunting of excess cerebrospinal fluid (CSF) in hopes of improving neurologic outcomes was attempted in the 1980s but was ...

    journal_title:Prenatal diagnosis

    pub_type: 杂志文章,评审

    doi:10.1002/pd.5527

    authors: Emery SP,Narayanan S,Greene S

    更新日期:2020-01-01 00:00:00

  • Prenatal DNA Sequencing: Clinical, Counseling, and Diagnostic Laboratory Considerations.

    abstract::Clinical diagnostic laboratories are producing next-generation sequencing-based test results that are becoming increasingly incorporated into patient care. Whole genome and exome sequencing on fetal material derived from amniocytes, chorionic villi, or products of conception is starting to be offered clinically in spe...

    journal_title:Prenatal diagnosis

    pub_type: 杂志文章,评审

    doi:10.1002/pd.5038

    authors: Abou Tayoun AN,Spinner NB,Rehm HL,Green RC,Bianchi DW

    更新日期:2018-01-01 00:00:00

  • An investigation of methods for enriching trophoblast from maternal blood.

    abstract::Trophoblast deportation is known to occur in normal human pregnancy, but it is not yet clear whether these cells routinely enter the maternal peripheral circulation and are available as a source of fetal DNA for non-invasive prenatal diagnosis of genetic disorders. To resolve this issue requires an efficient method of...

    journal_title:Prenatal diagnosis

    pub_type: 杂志文章

    doi:10.1002/pd.1970151007

    authors: Johansen M,Knight M,Maher EJ,Smith K,Sargent IL

    更新日期:1995-10-01 00:00:00

  • Trends in elective terminations of pregnancy between 1989 and 2000 in a French county (the Isère).

    abstract:OBJECTIVES:This study was performed in order to provide a description of indications for induced elective terminations of pregnancy (ETOP), their characteristics (e.g. gestational age), and their evolution over time. DESIGN OF THE STUDY:This is an epidemiological study. The geographic area covered is the French county...

    journal_title:Prenatal diagnosis

    pub_type: 杂志文章

    doi:10.1002/pd.711

    authors: Guillem P,Fabre B,Cans C,Robert-Gnansia E,Jouk PS

    更新日期:2003-11-01 00:00:00

  • Dehydro-oestriol and dehydropregnanetriol are candidate analytes for prenatal diagnosis of Smith-Lemli-Opitz syndrome.

    abstract::Gas chromatographic/mass spectrometric (GC/MS) analysis of maternal urine and serum steroids from 13 pregnancies at 25% risk for Smith-Lemli-Opitz syndrome (SLOS) was undertaken. All patients were between 12 and 31 weeks' gestational age. From dehydrocholesterol/cholesterol ratios determined in amniotic fluid and chor...

    journal_title:Prenatal diagnosis

    pub_type: 杂志文章

    doi:10.1002/1097-0223(200103)21:3<207::aid-pd27>3.0.co

    authors: Shackleton CH,Roitman E,Kratz L,Kelley R

    更新日期:2001-03-01 00:00:00

  • A comparison of amniotic fluid alpha-fetoprotein and acetylcholinesterase in the prenatal diagnosis of open neural tube defects and anterior abdominal wall defects.

    abstract::Amniotic fluid samples received for routine prenatal diagnosis of open neural tube defects were used for a study to compare amniotic fluid acetylcholinesterase (AChE) determination using a monoclonal antibody (4F19) enzyme antigen immunoassay and amniotic fluid alpha-fetoprotein (AFP) measurement as diagnostic tests f...

    journal_title:Prenatal diagnosis

    pub_type: 杂志文章

    doi:10.1002/pd.1970130204

    authors: Loft AG,Høgdall E,Larsen SO,Nørgaard-Pedersen B

    更新日期:1993-02-01 00:00:00