Literature DB >> 2293504

Biological roles of blood group antigens.

W L Marsh1.   

Abstract

Recognition and application of blood group differences on human red cells permitted the development of safe procedures for blood transfusion. Blood group antigens are markers on surface-exposed red cell proteins or the sugar moiety of glycoproteins or glycolipids. Apart from their presumed biological function, some antigens have been identified as receptors for host/parasite interactions. Thus, carbohydrates that determine P antigenicity are the binding receptor for certain strains of pyelonephritic coliforms. Other pathogenic coliforms bind to the membrane structure that carries the Dra antigen. A structure associated with Duffy antigens is the attachment receptor for the parasite of Plasmodium vivax malaria, while Plasmodium falciparum parasites bind to structures associated with membrane glycophorins. Structure/function relationships have been established by the finding that lack of Rh protein in red cells of Rhnull phenotype is associated with stomatocytic cell morphology and a hemolytic state. Absence of glycophorin C, and the Gerbich blood group antigens that it carries, is associated with elliptocytic red cells. Absence of Kx antigen protein in the Kell system is associated with the McLeod blood group phenotype, with acanthocytic cell morphology and reduced in vivo survival. McLeod individuals also have late-onset muscular dystrophy and neurological disorders.

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Year:  1990        PMID: 2293504      PMCID: PMC2589361     

Source DB:  PubMed          Journal:  Yale J Biol Med        ISSN: 0044-0086


  16 in total

1.  A new phenotype (McLeod) in the Kell blood-group system.

Authors:  F H ALLEN; S M KRABBE; P A CORCORAN
Journal:  Vox Sang       Date:  1961-09       Impact factor: 2.144

2.  Haematological changes associated with the McLeod phenotype of the Kell blood group system.

Authors:  B M Wimer; W L Marsh; H F Taswell; W R Galey
Journal:  Br J Haematol       Date:  1977-06       Impact factor: 6.998

3.  Multiple phenotypic abnormalities associated with Rh-null (---/---).

Authors:  P J Schmidt; G H Vos
Journal:  Vox Sang       Date:  1967-07       Impact factor: 2.144

4.  Glycophorin as a possible receptor for Plasmodium falciparum.

Authors:  G Pasvol; M Jungery; D J Weatherall; S F Parsons; D J Anstee; M J Tanner
Journal:  Lancet       Date:  1982-10-30       Impact factor: 79.321

5.  A possible null phenotype in the Cromer blood group complex.

Authors:  G L Daniels; H Tohyama; M Uchikawa
Journal:  Transfusion       Date:  1982 Sep-Oct       Impact factor: 3.157

6.  Structure of carbohydrate part of receptor on human uroepithelial cells for pyelonephritogenic Escherichia coli.

Authors:  G Källenius; S Svenson; R Möllby; B Cedergren; H Hultberg; J Winberg
Journal:  Lancet       Date:  1981-09-19       Impact factor: 79.321

7.  Elevated serum creatine phosphokinase in subjects with McLeod syndrome.

Authors:  W L Marsh; N J Marsh; A Moore; W A Symmans; C L Johnson; C M Redman
Journal:  Vox Sang       Date:  1981       Impact factor: 2.144

8.  A "new" phenotype confirming a relationship between Cra and Tca.

Authors:  C Levene; N Harel; G Lavie; S Greenberg; B Laird-Fryer; G L Daniels
Journal:  Transfusion       Date:  1984 Jan-Feb       Impact factor: 3.157

9.  Increased potassium transport and ouabain binding in human Rhnull red blood cells.

Authors:  P K Lauf; C H Joiner
Journal:  Blood       Date:  1976-09       Impact factor: 22.113

10.  Isolation of Kell-active protein from the red cell membrane.

Authors:  C M Redman; W L Marsh; K A Mueller; G P Avellino; C L Johnson
Journal:  Transfusion       Date:  1984 Mar-Apr       Impact factor: 3.157

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  1 in total

1.  The Incidence of Spontaneous Abortion in Mothers with Blood Group O Compared with other Blood Types.

Authors:  Mohammad Hassanzadeh-Nazarabadi; Sahar Shekouhi; Najmeh Seif
Journal:  Int J Mol Cell Med       Date:  2012
  1 in total

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