Literature DB >> 6755437

Phenotypic analysis of fetal blood leucocytes: potential for prenatal diagnosis of immunodeficiency disorders.

D C Linch, P C Beverley, R J Levinsky, C H Rodeck.   

Abstract

Recent technological advances allow the detection and quantitation of subsets of leucocytes using monoclonal antibodies. We have taken advantage of this to study the ontogeny of fetal blood leucocytes, using very small blood samples obtained at fetoscopy. By 14 weeks gestation T cells represent 35 per cent or more of fetal leucocytes and the distribution of the helper/inducer and suppressor/cytotoxic subsets is similar to that of adults. B lymphocytes before 16 1/2 weeks are low (4-20 per cent), but rise to a mean of 28 per cent in 17-26 week fetuses. Granulocytic cells, many of which are phenotypically immature, represent 18-34 per cent of total leucocytes. The methodology employed is very reliable and offers the opportunity for the prenatal diagnosis of some immunodeficiency disorders, since using the same reagents we have diagnosed children with severe combined immunodeficiency shortly after birth.

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Year:  1982        PMID: 6755437     DOI: 10.1002/pd.1970020310

Source DB:  PubMed          Journal:  Prenat Diagn        ISSN: 0197-3851            Impact factor:   3.050


  12 in total

Review 1.  Prenatal diagnosis and carrier detection in primary immunodeficiency disorders.

Authors:  Y L Lau; R J Levinsky
Journal:  Arch Dis Child       Date:  1988-07       Impact factor: 3.791

2.  The effects of pertussis toxin on human T lymphocytes.

Authors:  E A Macintyre; P E Tatham; R Abdul-Gaffar; D C Linch
Journal:  Immunology       Date:  1988-07       Impact factor: 7.397

3.  The effect of mitogenic lectins and monoclonal antibodies on intracellular free calcium concentration in human T-lymphocytes.

Authors:  K O'Flynn; D C Linch; P E Tatham
Journal:  Biochem J       Date:  1984-04-15       Impact factor: 3.857

4.  Use of monoclonal antibodies in a study of the development of T lymphocytes in the human fetus.

Authors:  G E Asma; R L Van den Bergh; J M Vossen
Journal:  Clin Exp Immunol       Date:  1983-08       Impact factor: 4.330

5.  Prenatal exclusion of severe combined immunodeficiency.

Authors:  R J Levinsky; D C Linch; C L Beverly; C Rodeck
Journal:  Arch Dis Child       Date:  1982-12       Impact factor: 3.791

6.  Binding of monoclonal antibody to CD16 causes calcium mobilization in large granular lymphocytes but inhibits NK killing.

Authors:  E A Macintyre; D W Wallace; K O'Flynn; R Abdul-Gaffar; P A Tetteroo; G Morgan; D C Linch
Journal:  Immunology       Date:  1989-03       Impact factor: 7.397

7.  Prenatal diagnosis of three cases of severe combined immunodeficiency: severe T cell deficiency during the first half of gestation in fetuses with adenosine deaminase deficiency.

Authors:  D C Linch; R J Levinsky; C H Rodeck; K A Maclennan; H A Simmonds
Journal:  Clin Exp Immunol       Date:  1984-05       Impact factor: 4.330

8.  Close linkage of random DNA fragments from Xq 21.3-22 to X-linked agammaglobulinaemia (XLA).

Authors:  S Malcolm; G de Saint Basile; B Arveiler; Y L Lau; P Szabo; A Fischer; C Griscelli; M Debre; J L Mandel; R E Callard
Journal:  Hum Genet       Date:  1987-10       Impact factor: 4.132

9.  Phorbol myristate acetate stimulated NBT test: a simple method suitable for antenatal diagnosis of chronic granulomatous disease.

Authors:  R J Levinsky; B A Harvey; C H Rodeck; J F Soothill
Journal:  Clin Exp Immunol       Date:  1983-11       Impact factor: 4.330

10.  Lymphocyte subpopulations in primary immunodeficiency disorders.

Authors:  E G Davies; R J Levinsky; M Butler; R M Thomas; D C Linch
Journal:  Arch Dis Child       Date:  1983-05       Impact factor: 3.791

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